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MB Sample ID: SA177866

Local Sample ID:0060_LC_20190903_sample_0001
Subject ID:SU001997
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090
Gender:Male and female

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Combined analysis:

Analysis ID AN003118
Analysis type MS
Chromatography type Reversed phase
Chromatography system Agilent 6545 LC/QTOF
Column Waters ACQUITY UPLC BEH C18
MS Type ESI
MS instrument type GC-TOF
MS instrument name Agilent 6545 LC/QTOF
Ion Mode UNSPECIFIED
Units Summarised value

MS:

MS ID:MS002899
Analysis ID:AN003118
Instrument Name:Agilent 6545 LC/QTOF
Instrument Type:GC-TOF
MS Type:ESI
MS Comments:The data processing included alignment of peaks, peak integration, normalization and identification. Lipids were identified using an internal spectral library. The data were normalized using one or more internal standards representative of each class of lipid present in the samples: the intensity of each identified lipid was normalized by dividing it with the intensity of its corresponding standard and multiplying it by the concentration of the standard. All monoacyl lipids except cholesterol esters, such as monoacylglycerols and monoacylglycerophospholipids, were normalized with PC(17:0/0:0), all diacyl lipids except ethanolamine phospholipids were normalized with PC(17:0/17:0), all ceramides with Cer(d18:1/17:0), all diacyl ethanolamine phospholipids with PE(17:0/17:0), and TG and cholesterol esters with TG(17:0/17:0/17:0). Other (unidentified) molecular species were normalized with PC(17:0/0:0) for retention times < 300 s, PC(17:0/17:0) for a retention time between 300 s and 410 s, and TG(17:0/17:0/17:0) for longer retention times. Quality control of the method showed that the day-to-day repeatability of control serum samples, and the relative standard deviation (RSD) for values identified was on average below 25% and 20% for discovery and validation sECs, respectively. The internal standards added to all samples in the study had an average RSD of 25% and 13 % in the discovery and validation sECs.
Ion Mode:UNSPECIFIED
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