{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST000768","ANALYSIS_ID":"AN001215","VERSION":"1","CREATED_ON":"July 5, 2017, 1:03 pm"},

"PROJECT":{"PROJECT_TITLE":"Metabolites of human neurons and stem cells (siNeuron metabolomics)","PROJECT_TYPE":"MS analysis","PROJECT_SUMMARY":"metabolites of human neurons and stem cells","INSTITUTE":"University of Michigan","DEPARTMENT":"Mol Behav Neurosci Inst","LABORATORY":"Uhler Lab","LAST_NAME":"Uhler","FIRST_NAME":"Michael","ADDRESS":"Ann Arbor, MI","EMAIL":"muhler@umich.edu","PHONE":"734-657-3192"},

"STUDY":{"STUDY_TITLE":"Metabolites of human neurons and stem cells (siNeuron metabolomics)","STUDY_TYPE":"MS analysis","STUDY_SUMMARY":"There are a total of four samples each for this analysis. Each sample consists of the cells grown on three 10 cm culture plates. Each plate should have 2x106 cells for a total of 6x106 cells per sample when all three plates are combined. The first sample is undifferentiated human embryonic stem cells, the second sample is human glutamatergic neurons derived from those human embryonic stem cells, the third sample is undifferentiated human induced pluripotent stem cells and the fourth sample is human glutamatergic neurons derived from those human induced pluripotent stem cells.","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":"4","TOTAL_SUBJECTS":"1"},

"SUBJECT":{"SUBJECT_TYPE":"HUMAN","SUBJECT_SPECIES":"Homo sapiens","TAXONOMY_ID":"9606"},
"SUBJECT_SAMPLE_FACTORS":[
{
"Subject ID":"SU0016366",
"Sample ID":"S00026210",
"Factors":{"Media":"E8 media","Type":"stem cells"}
},
{
"Subject ID":"SU0016366",
"Sample ID":"S00026211",
"Factors":{"Media":"3N media","Type":"neurons"}
},
{
"Subject ID":"SU0016366",
"Sample ID":"S00026212",
"Factors":{"Media":"E8 media","Type":"stem cells"}
},
{
"Subject ID":"SU0016366",
"Sample ID":"S00026213",
"Factors":{"Media":"3N media","Type":"neurons"}
}
],
"COLLECTION":{"COLLECTION_SUMMARY":"-"},

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

"SAMPLEPREP":{"SAMPLEPREP_SUMMARY":"-","SAMPLEPREP_PROTOCOL_FILENAME":"A003 - Untargeted Metabolomics.pdf"},

"CHROMATOGRAPHY":{"CHROMATOGRAPHY_TYPE":"Reversed phase","INSTRUMENT_NAME":"Agilent","COLUMN_NAME":"Waters Acquity HSS T3 (50 x 2.1mm, 1.8um)"},

"ANALYSIS":{"ANALYSIS_TYPE":"MS","ANALYSIS_PROTOCOL_FILE":"A003 - Untargeted Metabolomics.pdf"},

"MS":{"MS_COMMENTS":"-","INSTRUMENT_NAME":"Agilent 6530 QTOF","INSTRUMENT_TYPE":"QTOF","MS_TYPE":"ESI","ION_MODE":"POSITIVE"},

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

"Data":[{"Metabolite":"1-AMINOCYCLOPROPANE-1-CARBOXYLIC ACID (M+H)+","S00026210":"6998","S00026211":"7091","S00026212":"98331","S00026213":"95045"},{"Metabolite":"1-METHYLNICOTINAMIDE M+","S00026210":"","S00026211":"24624","S00026212":"","S00026213":"96194"},{"Metabolite":"1-METHYLXANTHINE (M+H)+","S00026210":"3409597","S00026211":"2847800","S00026212":"4300639","S00026213":"4217875"},{"Metabolite":"1-METHYLXANTHINE (M+NA)+","S00026210":"38216","S00026211":"36617","S00026212":"46279","S00026213":"49837"},{"Metabolite":"16:0 LYSO PC (M+H)+","S00026210":"161599","S00026211":"222225","S00026212":"88666","S00026213":"132678"},{"Metabolite":"16:0 LYSO PC (M+NA)+","S00026210":"86382","S00026211":"138208","S00026212":"49458","S00026213":"87424"},{"Metabolite":"16:0-18:0 PC (M+H)+","S00026210":"10348","S00026211":"264406","S00026212":"41064","S00026213":"308061"},{"Metabolite":"16:0-18:0 PC (M+NA)+","S00026210":"","S00026211":"118666","S00026212":"","S00026213":"121529"},{"Metabolite":"18:0 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}

}