{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST000685","ANALYSIS_ID":"AN001056","VERSION":"1","CREATED_ON":"June 30, 2017, 12:05 pm"},

"PROJECT":{"PROJECT_TITLE":"Molecular genetic study on nonalcoholic fatty liver disease (NAFLD)","PROJECT_TYPE":"MS analysis","PROJECT_SUMMARY":"In this study, we determine the genetic mechanism of action by which variants near GCKR and PPP1R3B exert their effects on promoting NAFLD","INSTITUTE":"University of Michigan","DEPARTMENT":"Internal Medicine","LABORATORY":"Speliotes Lab","LAST_NAME":"Speliotes","FIRST_NAME":"Elizabeth","ADDRESS":"Ann Arbor, MI","EMAIL":"espeliot@umich.edu","PHONE":"734-647-2964"},

"STUDY":{"STUDY_TITLE":"Lipidomics analysis for human liver cell lines","STUDY_TYPE":"MS analysis","STUDY_SUMMARY":"On day 1, seed 1 million cells/dish Huh7_Lok cells (vector, GCKR(WT), GCKR(P446L), Non-Target, GCKR KD and PPP1R3B/OE) in 100 mm dishes with DMEM complete medium and incubate at 37C for 24 h. On day 2, replace DMEM medium with delipidated serum medium for these cells and incubate for another 24 h. On day 3, add heated Oleic Acid-Albumin into each dish at final concentration of 200?M for 24h. On day 4, collect cells with Trypsin/EDTA lysis and count cells with automated cell counter and calculate total cell numbers in each sample, then centrifuge cells down and take out the supernatant and keep cells in -80 C freezer.","INSTITUTE":"University of Michigan","DEPARTMENT":"Biomedical Research Core Facilities","LABORATORY":"Metabolomics core","LAST_NAME":"Kachman","FIRST_NAME":"Maureen","ADDRESS":"6300 Brehm Tower, 1000 Wall Street, Ann Arbor, MI 48105-5714","EMAIL":"mkachman@med.umich.edu","PHONE":"(734) 232-8175","NUM_GROUPS":"6","TOTAL_SUBJECTS":"1"},

"SUBJECT":{"SUBJECT_TYPE":"Human","SUBJECT_SPECIES":"Homo sapiens","TAXONOMY_ID":"9606"},
"SUBJECT_SAMPLE_FACTORS":[
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"Subject ID":"SU0017688",
"Sample ID":"S00027752",
"Factors":{"Construct":"Vector"}
},
{
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"Sample ID":"S00027753",
"Factors":{"Construct":"Vector"}
},
{
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"Sample ID":"S00027754",
"Factors":{"Construct":"Vector"}
},
{
"Subject ID":"SU0017688",
"Sample ID":"S00027755",
"Factors":{"Construct":"GCKR(WT)"}
},
{
"Subject ID":"SU0017688",
"Sample ID":"S00027756",
"Factors":{"Construct":"GCKR(WT)"}
},
{
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"Sample ID":"S00027757",
"Factors":{"Construct":"GCKR(WT)"}
},
{
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"Sample ID":"S00027758",
"Factors":{"Construct":"GCKR(P446L)"}
},
{
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"Sample ID":"S00027759",
"Factors":{"Construct":"GCKR(P446L)"}
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"Sample ID":"S00027760",
"Factors":{"Construct":"GCKR(P446L)"}
},
{
"Subject ID":"SU0017688",
"Sample ID":"S00027761",
"Factors":{"Construct":"PPP1R3B"}
},
{
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"Sample ID":"S00027762",
"Factors":{"Construct":"PPP1R3B"}
},
{
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"Sample ID":"S00027763",
"Factors":{"Construct":"NT"}
},
{
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"Sample ID":"S00027764",
"Factors":{"Construct":"NT"}
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{
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"Sample ID":"S00027765",
"Factors":{"Construct":"NT"}
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{
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"Sample ID":"S00027766",
"Factors":{"Construct":"GCKR_52621"}
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{
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"Sample ID":"S00027767",
"Factors":{"Construct":"GCKR_52621"}
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{
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"Sample ID":"S00027768",
"Factors":{"Construct":"GCKR_52621"}
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],
"COLLECTION":{"COLLECTION_SUMMARY":"-"},

"TREATMENT":{"TREATMENT_SUMMARY":"-"},

"SAMPLEPREP":{"SAMPLEPREP_SUMMARY":"-","SAMPLEPREP_PROTOCOL_FILENAME":"A004 - Shotgun Lipidomics.pdf"},

"CHROMATOGRAPHY":{"CHROMATOGRAPHY_TYPE":"Reversed phase","INSTRUMENT_NAME":"ABI Sciex 5600+ TripleTOF","COLUMN_NAME":"Waters Acquity HSS T3 (50 x 2.1mm, 1.8um)"},

"ANALYSIS":{"ANALYSIS_TYPE":"MS","ANALYSIS_PROTOCOL_FILE":"A004 - Shotgun Lipidomics.pdf"},

"MS":{"MS_COMMENTS":"-","INSTRUMENT_NAME":"ABI Sciex 5600+ TripleTOF","INSTRUMENT_TYPE":"Triple TOF","MS_TYPE":"ESI","ION_MODE":"NEGATIVE"},

"MS_METABOLITE_DATA":{
"Units":"peak area normalized",

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}