{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST000702","ANALYSIS_ID":"AN001092","VERSION":"1","CREATED_ON":"July 1, 2017, 5:22 pm"},

"PROJECT":{"PROJECT_TITLE":"NIH 3T3 fibroblast cells with Ceftriaxone Treatment","PROJECT_TYPE":"MS analysis","PROJECT_SUMMARY":"3T3 cells treated with 50uM Ceftriaxone for 24hrs, 1hr, or 0 hrs.","INSTITUTE":"Vanderbilt University","DEPARTMENT":"Pharmacology","LABORATORY":"Blakely Lab","LAST_NAME":"Blakely","FIRST_NAME":"Randy","ADDRESS":"Nashville, TN","EMAIL":"randy.blakely@vanderbilt.edu","PHONE":"615-936-1700"},

"STUDY":{"STUDY_TITLE":"NIH 3T3 fibroblast cells with Ceftriaxone Treatment","STUDY_TYPE":"MS analysis","STUDY_SUMMARY":"NIH 3T3 cells were plated at 1.5million cells per 10cM dish into 12 10cm dishes. 24hrs post plating media was changed on all plates. At the time of media change, 4 dishes were treated with a final concentration of 50uM ceftriaxone (24hrs ceftriaxone n=4). 23 hrs post media change, 4 separate dishes were treated with 50uM ceftriaxone for 1hr (1hr ceftriaxone n=4). 4 dishes were untreated (0hr, basal, n=4). 24 hrs post media change, media was quickly removed from all 12 plates, each plate was rapidly washed with MilliQ H2O and rapidly frozen with liquid nitrogen poured directly into the dishes. All plates were transferred to dry ice and stored at -80 until shipped.","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":"3","TOTAL_SUBJECTS":"2"},

"SUBJECT":{"SUBJECT_TYPE":"Mouse","SUBJECT_SPECIES":"Mus musculus","TAXONOMY_ID":"10088"},
"SUBJECT_SAMPLE_FACTORS":[
{
"Subject ID":"SU0012748",
"Sample ID":"S00019331",
"Factors":{"Timepoint":"0hr"}
},
{
"Subject ID":"SU0012748",
"Sample ID":"S00019332",
"Factors":{"Timepoint":"0hr"}
},
{
"Subject ID":"SU0012748",
"Sample ID":"S00019333",
"Factors":{"Timepoint":"0hr"}
},
{
"Subject ID":"SU0012748",
"Sample ID":"S00019334",
"Factors":{"Timepoint":"0hr"}
},
{
"Subject ID":"SU0012748",
"Sample ID":"S00019335",
"Factors":{"Timepoint":"1hr"}
},
{
"Subject ID":"SU0012748",
"Sample ID":"S00019336",
"Factors":{"Timepoint":"1hr"}
},
{
"Subject ID":"SU0012748",
"Sample ID":"S00019337",
"Factors":{"Timepoint":"1hr"}
},
{
"Subject ID":"SU0012748",
"Sample ID":"S00019338",
"Factors":{"Timepoint":"1hr"}
},
{
"Subject ID":"SU0012748",
"Sample ID":"S00019339",
"Factors":{"Timepoint":"24hr"}
},
{
"Subject ID":"SU0012748",
"Sample ID":"S00019340",
"Factors":{"Timepoint":"24hr"}
},
{
"Subject ID":"SU0012748",
"Sample ID":"S00019341",
"Factors":{"Timepoint":"24hr"}
},
{
"Subject ID":"SU0012748",
"Sample ID":"S00019342",
"Factors":{"Timepoint":"24hr"}
},
{
"Subject ID":"SU9999996",
"Sample ID":"S00020154",
"Factors":{"Timepoint":"-"}
}
],
"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 normalized",

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}

}