<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<jPostDataset id="JPST000938" formatVersion="1.0">
  <Project id="JPST000938" pxid="PXD020851" createdDate="2020-08-11" modifiedDate="2020-08-12" mode="partial" jpostRevision="0" type="Mass spectrometry" announced="true">
    <Title>Time course treatment with Palmitate and thapsigargin of insulinoma INS-1E cells</Title>
    <Description>Time course treatment with 0.4 mM Palmitate and 200 nM thapsigargin of insulinoma INS-1E cells. Timepoints; 0, 4, 16 and 24h in biological duplicates within an iTRAQ 8 set for palmitate and thapsigargin, respectively. &#10;</Description>
    <AnnouncementDate>2020-08-18</AnnouncementDate>
    <Note/>
  </Project>
  <presetSummary>
    <Species>
      <PresetElement id="10117" value="Rattus rattus (Black rat)"/>
    </Species>
    <Instrument>
      <PresetElement id="MS:1001742" value="LTQ Orbitrap Velos"/>
    </Instrument>
    <Modification>
      <PresetElement id="MOD:01060" ontologyName="S-carboxamidomethyl-L-cysteine" value="Carbamidomethyl (C)"/>
      <PresetElement id="MOD:00719" ontologyName="L-methionine sulfoxide" value="Oxidation (M)"/>
      <PresetElement id="MOD:01710" ontologyName="iTRAQ8plex reporter+balance reagent N-acylated residue" value="iTRAQ8plex (K)"/>
      <PresetElement id="MOD:01712" ontologyName="iTRAQ8plex reporter+balance reagent acylated N-terminal" value="iTRAQ8plex (N-term)"/>
    </Modification>
  </presetSummary>
  <Contact>
    <Name>Henrik Johansson</Name>
    <Affiliation>Karolinska Institutet</Affiliation>
    <PrincipalInvestigator>Janne Lehtiö</PrincipalInvestigator>
  </Contact>
  <Relation>
    <Keywords>Palmitate, thapsigargin, insulinoma, diabetes</Keywords>
    <PubMed/>
  </Relation>
  <FileList>
    <File id="f_0000581449">
      <Name>100702_VR_Palm_fr_11.raw</Name>
      <Type>raw</Type>
      <Size>453879808</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Name>100702_VR_Palm_fr_12.raw</Name>
      <Type>raw</Type>
      <Size>424600814</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581451">
      <Name>100709_VR_Palm_60min_Fr_13.raw</Name>
      <Type>raw</Type>
      <Size>475553449</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581452">
      <Name>100709_VR_Palm_60min_Fr_14.raw</Name>
      <Type>raw</Type>
      <Size>492987497</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581453">
      <Name>100709_VR_Palm_60min_Fr_15.raw</Name>
      <Type>raw</Type>
      <Size>445700502</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
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        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
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          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
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      </Profile>
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        <Sample id="S0000002175">
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          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
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          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
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      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
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        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
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      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
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          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
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      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
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          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
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      </Profile>
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        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
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          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
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      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
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          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
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      </Profile>
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        <Sample id="S0000002175">
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          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
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          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
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          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581456">
      <Name>100709_VR_Palm_60min_Fr_18.raw</Name>
      <Type>raw</Type>
      <Size>352385299</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581457">
      <Name>100709_VR_Palm_60min_Fr_19.raw</Name>
      <Type>raw</Type>
      <Size>389505480</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581458">
      <Name>100709_VR_Palm_60min_Fr_20.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581459">
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581461">
      <Name>100709_VR_Palm_90min_fr_17.raw</Name>
      <Type>raw</Type>
      <Size>504787405</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581462">
      <Name>100709_VR_Palm_90min_fr_23.raw</Name>
      <Type>raw</Type>
      <Size>636042178</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581463">
      <Name>100709_VR_Palm_90min_fr_24.raw</Name>
      <Type>raw</Type>
      <Size>516542419</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581464">
      <Name>100709_VR_Palm_90min_fr_25.raw</Name>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581466">
      <Name>100710_VR_Palm_60min_fr_32.raw</Name>
      <Type>raw</Type>
      <Size>391960344</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581467">
      <Name>100710_VR_Palm_60min_fr_33.raw</Name>
      <Type>raw</Type>
      <Size>386083316</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581468">
      <Name>100710_VR_Palm_60min_fr_34.raw</Name>
      <Type>raw</Type>
      <Size>350011778</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581469">
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        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
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      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
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        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
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      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
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          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
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      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
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      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
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      </Profile>
    </File>
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      <Size>395306850</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581471">
      <Name>100710_VR_Palm_60min_fr_37.raw</Name>
      <Type>raw</Type>
      <Size>358005204</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581472">
      <Name>100710_VR_Palm_60min_fr_38.raw</Name>
      <Type>raw</Type>
      <Size>368880885</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581473">
      <Name>100710_VR_Palm_60min_fr_39.raw</Name>
      <Type>raw</Type>
      <Size>350060133</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581474">
      <Name>100710_VR_Palm_60min_fr_40.raw</Name>
      <Type>raw</Type>
      <Size>366217895</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Name>100710_VR_Palm_60min_fr_41.raw</Name>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
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      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
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      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
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      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
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      </Profile>
    </File>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
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      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581477">
      <Name>100710_VR_Palm_60min_fr_43.raw</Name>
      <Type>raw</Type>
      <Size>357098043</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581478">
      <Name>100710_VR_Palm_60min_fr_60.raw</Name>
      <Type>raw</Type>
      <Size>379546363</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581479">
      <Name>100710_VR_Palm_60min_fr_61.raw</Name>
      <Type>raw</Type>
      <Size>423081246</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581480">
      <Name>100710_VR_Palm_60min_fr_62.raw</Name>
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        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
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      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
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      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
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      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
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          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581482">
      <Name>100710_VR_Palm_60min_fr_64.raw</Name>
      <Type>raw</Type>
      <Size>447054912</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581483">
      <Name>100710_VR_Palm_60min_fr_65.raw</Name>
      <Type>raw</Type>
      <Size>377724245</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581484">
      <Name>100710_VR_Palm_60min_fr_66.raw</Name>
      <Type>raw</Type>
      <Size>392779784</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581485">
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        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
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      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
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      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
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      </Profile>
    </File>
    <File id="f_0000581486">
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
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      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581487">
      <Name>100710_VR_Palm_60min_fr_69.raw</Name>
      <Type>raw</Type>
      <Size>402437833</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581488">
      <Name>100710_VR_Palm_90min_fr_28.raw</Name>
      <Type>raw</Type>
      <Size>511217029</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581489">
      <Name>100710_VR_Palm_90min_fr_29.raw</Name>
      <Type>raw</Type>
      <Size>527244451</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581490">
      <Name>100710_VR_Palm_90min_fr_30.raw</Name>
      <Type>raw</Type>
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        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581492">
      <Name>100710_VR_Palm_90min_fr_44.raw</Name>
      <Type>raw</Type>
      <Size>488909805</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581493">
      <Name>100710_VR_Palm_90min_fr_45.raw</Name>
      <Type>raw</Type>
      <Size>526425145</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581494">
      <Name>100710_VR_Palm_90min_fr_46.raw</Name>
      <Type>raw</Type>
      <Size>441975385</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581495">
      <Name>100710_VR_Palm_90min_fr_47.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581496">
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      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581497">
      <Name>100710_VR_Palm_90min_fr_49.raw</Name>
      <Type>raw</Type>
      <Size>464160162</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581498">
      <Name>100710_VR_Palm_90min_fr_50.raw</Name>
      <Type>raw</Type>
      <Size>509045929</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581499">
      <Name>100710_VR_Palm_90min_fr_51.raw</Name>
      <Type>raw</Type>
      <Size>452918315</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581500">
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        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
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      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
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      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
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      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Size>470614468</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581502">
      <Name>100710_VR_Palm_90min_fr_54.raw</Name>
      <Type>raw</Type>
      <Size>481326089</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581503">
      <Name>100710_VR_Palm_90min_fr_55.raw</Name>
      <Type>raw</Type>
      <Size>484748695</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581504">
      <Name>100710_VR_Palm_90min_fr_56.raw</Name>
      <Type>raw</Type>
      <Size>504524975</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581505">
      <Name>100710_VR_Palm_90min_fr_57.raw</Name>
      <Type>raw</Type>
      <Size>507480660</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581506">
      <Name>100710_VR_Palm_90min_fr_58.raw</Name>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
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      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
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      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
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      </Profile>
    </File>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
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      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581508">
      <Name>100819_VR_Palm_60min_fr_25.raw</Name>
      <Type>raw</Type>
      <Size>665118019</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581509">
      <Name>100819_VR_Palm_60min_fr_26.raw</Name>
      <Type>raw</Type>
      <Size>550692389</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581510">
      <Name>100819_VR_Palm_60min_fr_27.raw</Name>
      <Type>raw</Type>
      <Size>559989979</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581511">
      <Name>100819_VR_Palm_60min_fr_28.raw</Name>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
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      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
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      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581513">
      <Name>100819_VR_Palm_60min_fr_30.raw</Name>
      <Type>raw</Type>
      <Size>547326405</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581514">
      <Name>100819_VR_Palm_60min_fr_31.raw</Name>
      <Type>raw</Type>
      <Size>562622963</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581515">
      <Name>100819_VR_Palm_60min_fr_32.raw</Name>
      <Type>raw</Type>
      <Size>563356173</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581516">
      <Name>100819_VR_Palm_60min_fr_33.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581517">
      <Name>100819_VR_Palm_60min_fr_35.raw</Name>
      <Type>raw</Type>
      <Size>600996775</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581518">
      <Name>100819_VR_Palm_60min_fr_36.raw</Name>
      <Type>raw</Type>
      <Size>523138661</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581519">
      <Name>100819_VR_Palm_60min_fr_37.raw</Name>
      <Type>raw</Type>
      <Size>567783061</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581520">
      <Name>100819_VR_Palm_60min_fr_38.raw</Name>
      <Type>raw</Type>
      <Size>546882784</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581521">
      <Name>100819_VR_Palm_60min_fr_39.raw</Name>
      <Type>raw</Type>
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        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
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      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581523">
      <Name>100702_VR_Palm_fr_5.raw</Name>
      <Type>raw</Type>
      <Size>454546816</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581524">
      <Name>100702_VR_Palm_fr_6.raw</Name>
      <Type>raw</Type>
      <Size>229421899</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581525">
      <Name>100702_VR_Palm_fr_7.raw</Name>
      <Type>raw</Type>
      <Size>402746760</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581526">
      <Name>100702_VR_Palm_fr_8.raw</Name>
      <Type>raw</Type>
      <Size>495034255</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581527">
      <Name>100702_VR_Palm_fr_9.raw</Name>
      <Type>raw</Type>
      <Size>437276575</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581528">
      <Name>100702_VR_Palm_fr_10.raw</Name>
      <Type>raw</Type>
      <Size>327968471</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581529">
      <Name>100624_VR_Thaps_fr_04.raw</Name>
      <Type>raw</Type>
      <Size>836477022</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581530">
      <Name>100624_VR_Thaps_fr_05.raw</Name>
      <Type>raw</Type>
      <Size>579442223</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581531">
      <Name>100624_VR_Thaps_fr_06.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581533">
      <Name>100624_VR_Thaps_fr_08.raw</Name>
      <Type>raw</Type>
      <Size>471123909</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581534">
      <Name>100624_VR_Thaps_fr_09.raw</Name>
      <Type>raw</Type>
      <Size>404484144</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581535">
      <Name>100624_VR_Thaps_fr_10.raw</Name>
      <Type>raw</Type>
      <Size>469284151</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581536">
      <Name>100624_VR_Thaps_fr_11.raw</Name>
      <Type>raw</Type>
      <Size>395690380</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Name>100624_VR_Thaps_fr_12.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
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      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
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      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581539">
      <Name>100624_VR_Thaps_fr_14.raw</Name>
      <Type>raw</Type>
      <Size>296577678</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581540">
      <Name>100624_VR_Thaps_fr_15.raw</Name>
      <Type>raw</Type>
      <Size>283263677</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581541">
      <Name>100624_VR_Thaps_fr_16.raw</Name>
      <Type>raw</Type>
      <Size>299745529</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581542">
      <Name>100624_VR_Thaps_fr_17.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581544">
      <Name>100624_VR_Thaps_fr_19.raw</Name>
      <Type>raw</Type>
      <Size>292532953</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581545">
      <Name>100624_VR_Thaps_fr_20.raw</Name>
      <Type>raw</Type>
      <Size>296282877</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581546">
      <Name>100624_VR_Thaps_fr_21.raw</Name>
      <Type>raw</Type>
      <Size>321406809</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581547">
      <Name>100624_VR_Thaps_fr_22.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
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      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
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      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581549">
      <Name>100624_VR_Thaps_fr_24.raw</Name>
      <Type>raw</Type>
      <Size>404185641</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581550">
      <Name>100624_VR_Thaps_fr_25.raw</Name>
      <Type>raw</Type>
      <Size>418905015</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581551">
      <Name>100624_VR_Thaps_fr_26.raw</Name>
      <Type>raw</Type>
      <Size>383141077</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581552">
      <Name>100624_VR_Thaps_fr_27.raw</Name>
      <Type>raw</Type>
      <Size>352021577</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581553">
      <Name>100624_VR_Thaps_fr_28_1st_after_cal.raw</Name>
      <Type>raw</Type>
      <Size>522314104</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581554">
      <Name>100624_VR_Thaps_fr_29.raw</Name>
      <Type>raw</Type>
      <Size>393527428</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581555">
      <Name>100624_VR_Thaps_fr_30.raw</Name>
      <Type>raw</Type>
      <Size>355966903</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581556">
      <Name>100624_VR_Thaps_fr_31.raw</Name>
      <Type>raw</Type>
      <Size>364276377</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581557">
      <Name>100624_VR_Thaps_fr_32.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581558">
      <Name>100624_VR_Thaps_fr_33.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581559">
      <Name>100624_VR_Thaps_fr_34.raw</Name>
      <Type>raw</Type>
      <Size>327029813</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581560">
      <Name>100624_VR_Thaps_fr_35.raw</Name>
      <Type>raw</Type>
      <Size>348754574</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581561">
      <Name>100624_VR_Thaps_fr_36.raw</Name>
      <Type>raw</Type>
      <Size>354102189</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581562">
      <Name>100624_VR_Thaps_fr_37.raw</Name>
      <Type>raw</Type>
      <Size>343042059</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581563">
      <Name>100624_VR_Thaps_fr_38.raw</Name>
      <Type>raw</Type>
      <Size>337736526</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581564">
      <Name>100624_VR_Thaps_fr_39.raw</Name>
      <Type>raw</Type>
      <Size>351987726</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581565">
      <Name>100624_VR_Thaps_fr_40.raw</Name>
      <Type>raw</Type>
      <Size>340503030</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581566">
      <Name>100624_VR_Thaps_fr_40_2.raw</Name>
      <Type>raw</Type>
      <Size>361885642</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581567">
      <Name>100624_VR_Thaps_fr_41.raw</Name>
      <Type>raw</Type>
      <Size>355311351</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581568">
      <Name>100624_VR_Thaps_fr_42.raw</Name>
      <Type>raw</Type>
      <Size>350054270</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581569">
      <Name>100624_VR_Thaps_fr_43.raw</Name>
      <Type>raw</Type>
      <Size>361556983</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581570">
      <Name>100624_VR_Thaps_fr_44.raw</Name>
      <Type>raw</Type>
      <Size>335585233</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581571">
      <Name>100624_VR_Thaps_fr_45.raw</Name>
      <Type>raw</Type>
      <Size>333652640</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581572">
      <Name>100624_VR_Thaps_fr_46.raw</Name>
      <Type>raw</Type>
      <Size>320741163</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581573">
      <Name>100624_VR_Thaps_fr_47.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581574">
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      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581575">
      <Name>100624_VR_Thaps_fr_49.raw</Name>
      <Type>raw</Type>
      <Size>336554200</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581576">
      <Name>100624_VR_Thaps_fr_50.raw</Name>
      <Type>raw</Type>
      <Size>337599773</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581577">
      <Name>100624_VR_Thaps_fr_51.raw</Name>
      <Type>raw</Type>
      <Size>330812557</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581578">
      <Name>100624_VR_Thaps_fr_52.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
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      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581580">
      <Name>100624_VR_Thaps_fr_54.raw</Name>
      <Type>raw</Type>
      <Size>327919772</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581581">
      <Name>100624_VR_Thaps_fr_55.raw</Name>
      <Type>raw</Type>
      <Size>440526862</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581582">
      <Name>100624_VR_Thaps_fr_56.raw</Name>
      <Type>raw</Type>
      <Size>505105004</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581583">
      <Name>100624_VR_Thaps_fr_57.raw</Name>
      <Type>raw</Type>
      <Size>504858172</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581584">
      <Name>100624_VR_Thaps_fr_58.raw</Name>
      <Type>raw</Type>
      <Size>520798124</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581585">
      <Name>100624_VR_Thaps_fr_59.raw</Name>
      <Type>raw</Type>
      <Size>463735518</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581586">
      <Name>100624_VR_Thaps_fr_60.raw</Name>
      <Type>raw</Type>
      <Size>404510997</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581587">
      <Name>100624_VR_Thaps_fr_61.raw</Name>
      <Type>raw</Type>
      <Size>715178210</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581588">
      <Name>100624_VR_Thaps_fr_62.raw</Name>
      <Type>raw</Type>
      <Size>427827135</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Name>100624_VR_Thaps_fr_63.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581590">
      <Name>100624_VR_Thaps_fr_64.raw</Name>
      <Type>raw</Type>
      <Size>475485913</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581591">
      <Name>100624_VR_Thaps_fr_65.raw</Name>
      <Type>raw</Type>
      <Size>485625701</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581592">
      <Name>100624_VR_Thaps_fr_66.raw</Name>
      <Type>raw</Type>
      <Size>472691318</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581593">
      <Name>100624_VR_Thaps_fr_67.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581595">
      <Name>100624_VR_Thaps_fr_69.raw</Name>
      <Type>raw</Type>
      <Size>444926153</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581596">
      <Name>100818_VR_Thaps_60min_fr25.raw</Name>
      <Type>raw</Type>
      <Size>710417642</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581597">
      <Name>100818_VR_Thaps_60min_fr26.raw</Name>
      <Type>raw</Type>
      <Size>523920435</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581598">
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Size>540546741</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581600">
      <Name>100818_VR_Thaps_60min_fr29.raw</Name>
      <Type>raw</Type>
      <Size>511641747</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581601">
      <Name>100818_VR_Thaps_60min_fr30.raw</Name>
      <Type>raw</Type>
      <Size>510382385</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581602">
      <Name>100818_VR_Thaps_60min_fr31.raw</Name>
      <Type>raw</Type>
      <Size>537322027</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581603">
      <Name>100818_VR_Thaps_60min_fr32.raw</Name>
      <Type>raw</Type>
      <Size>562453337</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581604">
      <Name>100818_VR_Thaps_60min_fr33.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581606">
      <Name>100818_VR_Thaps_60min_fr35.raw</Name>
      <Type>raw</Type>
      <Size>549865987</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581607">
      <Name>100818_VR_Thaps_60min_fr36.raw</Name>
      <Type>raw</Type>
      <Size>558890014</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581608">
      <Name>100818_VR_Thaps_60min_fr37.raw</Name>
      <Type>raw</Type>
      <Size>555082844</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581609">
      <Name>100818_VR_Thaps_60min_fr38.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581611">
      <Name>100818_VR_Thaps_60min_fr40.raw</Name>
      <Type>raw</Type>
      <Size>545769725</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581612">
      <Name>100618_VR_Thaps_IPG34to48_fr_07.raw</Name>
      <Type>raw</Type>
      <Size>820086404</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581613">
      <Name>100618_VR_Thaps_IPG34to48_fr_09.raw</Name>
      <Type>raw</Type>
      <Size>759870407</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581614">
      <Name>100618_VR_Thaps_IPG34to48_fr_10.raw</Name>
      <Type>raw</Type>
      <Size>666136951</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581615">
      <Name>100618_VR_Thaps_IPG34to48_fr_11.raw</Name>
      <Type>raw</Type>
      <Size>666341783</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581616">
      <Name>100618_VR_Thaps_IPG34to48_fr_12.raw</Name>
      <Type>raw</Type>
      <Size>982573524</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581617">
      <Name>100624_VR_Thaps_fr_01.raw</Name>
      <Type>raw</Type>
      <Size>600810512</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581618">
      <Name>100624_VR_Thaps_fr_02.raw</Name>
      <Type>raw</Type>
      <Size>575925633</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581619">
      <Name>100624_VR_Thaps_fr_03.raw</Name>
      <Type>raw</Type>
      <Size>846010143</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000566">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide fraction="72" replicate="">IPG-IEF pH 3.4-4.8 fractionation</peptide>
          <note>The iTRAQ labelled peptides were separated by immobilized pH gradient - isoelectric focusing (IPG-IEF) on a 3.4-4.8 strip. Peptides were extracted from the strips into 72 fractions by a prototype liquid handling robot, supplied by GE Healthcare Bio-Sciences AB. A plastic device with 72 wells was put onto each strip and 50 µl of ultra-pure water (Milli-Q, Millipore) was added to each well. After 30 minutes incubation, the liquid was transferred to a 96 well plate and the extraction was repeated 2 more times. The extracted peptides were dried in a SpeedVac vaccum concentrator and dissolved in 3% acetronitrile (ACN), 0.1 % formic acid.</note>
          <title>IPG-IEF pH 3.4-4.8</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581620">
      <Name>100514_VR_Palm_4h_2microg.raw</Name>
      <Type>raw</Type>
      <Size>1557459337</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581621">
      <Name>100514_VR_Palm_4h_from5_2microg.raw</Name>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
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        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
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      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
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      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
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      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581622">
      <Name>100426_VR_Palm_4h_2microg.raw</Name>
      <Type>raw</Type>
      <Size>1612798577</Size>
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        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581623">
      <Name>100514_VR_Thaps_4h_2microg.raw</Name>
      <Type>raw</Type>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581624">
      <Name>100514_VR_Thaps_4h_from5_2microg.raw</Name>
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      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
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      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
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        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
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      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
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        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
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      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581625">
      <Name>100426_VR_Thaps_4h_2microg.raw</Name>
      <Type>raw</Type>
      <Size>1597002638</Size>
      <Profile plex="iTRAQ 113">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="1">iTRAQ 113</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 114">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="2">iTRAQ 114</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 115">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="3">iTRAQ 115</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 116">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="4">iTRAQ 116</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 117">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="5">iTRAQ 117</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 118">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="6">iTRAQ 118</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 119">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="7">iTRAQ 119</label>
        </MS_mode>
      </Profile>
      <Profile plex="iTRAQ 121">
        <Sample id="S0000002175">
          <species id="10117">Rattus rattus (Black rat)</species>
          <tissue id="BTO:0000214">cell culture</tissue>
          <celltype>insulinoma</celltype>
          <disease>diabetes</disease>
          <note>Treatment with palmitate or thapsigargin for 0, 4, 16 and 24 hours in duplicates.</note>
          <title>Time course experiment of INS-1E cells</title>
        </Sample>
        <Fractionation id="F0000000130">
          <subcellular replicate="">Whole</subcellular>
          <protein replicate=""/>
          <peptide replicate="">240 min RP gradient</peptide>
          <note>The TMT labelled peptides were separated by a 240 min gradient before analysis by MS. </note>
          <title>Long gradient separation - 4hrs</title>
        </Fractionation>
        <Enzyme_Mod id="E0000000561">
          <enzyme id="MS:1001251">Trypsin</enzyme>
          <fixedModification id="MOD:01060" name="S-carboxamidomethyl-L-cysteine">Carbamidomethyl (C)</fixedModification>
          <variableModification id="MOD:00719" name="L-methionine sulfoxide">Oxidation (M)</variableModification>
          <taxonomy id="10117">Rattus rattus (Black rat)</taxonomy>
          <note/>
          <fixedModification id="MOD:01710" name="iTRAQ8plex reporter+balance reagent N-acylated residue">iTRAQ8plex (K)</fixedModification>
          <fixedModification id="MOD:01712" name="iTRAQ8plex reporter+balance reagent acylated N-terminal">iTRAQ8plex (N-term)</fixedModification>
          <title>iTRAQ 8 - Rat</title>
        </Enzyme_Mod>
        <MS_mode id="M0000000141">
          <instrument id="MS:1001742">LTQ Orbitrap Velos</instrument>
          <instrumentMode>DDA-high res.</instrumentMode>
          <purpose>Relative quantification</purpose>
          <quantificationPlatform>Product ion (reporter quantification)</quantificationPlatform>
          <plex>8</plex>
          <note>See excel file with protein search results for sample assignments to each iTRAQ tag.</note>
          <title>LTQ Orbitrap - iTRAQ8</title>
          <label id="8">iTRAQ 121</label>
        </MS_mode>
      </Profile>
    </File>
    <File id="f_0000581626">
      <Name>VR_Thaps_IPG-IEF_fr1-69_3x4h_uniprot_rat.msf</Name>
      <Type>result</Type>
      <Size>8252215296</Size>
      <Profile/>
      <Format/>
      <Software>Proteome Discoverer 1.3</Software>
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      <Type>result</Type>
      <Size>9786109952</Size>
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      <Format/>
      <Software>Proteome Discoverer 1.3</Software>
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      <Format/>
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      <Format/>
      <Software>Proteome Discoverer 1.3</Software>
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      <Format>other</Format>
      <Software>Proteome Discoverer 1.3</Software>
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