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MB Sample ID: SA256104
| Local Sample ID: | D_Serum_24 |
| Subject ID: | SU002650 |
| Subject Type: | Human |
| Subject Species: | Homo sapiens |
| Taxonomy ID: | 9606 |
| Gender: | Male and female |
Select appropriate tab below to view additional metadata details:
Combined analysis:
| Analysis ID | AN004198 | AN004199 |
|---|---|---|
| Analysis type | MS | MS |
| Chromatography type | Reversed phase | Reversed phase |
| Chromatography system | Agilent 1290 | Agilent 1290 |
| Column | Agilent ZORBAX Eclipse Plus C18 (50 x 2.1mm,1.8um) | Agilent Pursuit 5 C18 (150 x 2.1mm,5um) |
| MS Type | ESI | ESI |
| MS instrument type | QTRAP | QTRAP |
| MS instrument name | ABI Sciex 5500 QTrap | ABI Sciex 5500 QTrap |
| Ion Mode | POSITIVE | POSITIVE |
| Units | nM | nM |
MS:
| MS ID: | MS003945 |
| Analysis ID: | AN004198 |
| Instrument Name: | ABI Sciex 5500 QTrap |
| Instrument Type: | QTRAP |
| MS Type: | ESI |
| MS Comments: | Data analysis was performed using Analyst 1.5.2 software. Extracted ion chromatograms (EIC) corresponding to each metabolite were used for quantitation (MRM). The area under the curve of each EIC was normalized to that of the internal standard. For metabolites related to PC/PE profiling, the peak area ratio of each metabolite to that of the internal standard was used for a relative comparison. For plasmalogens, the calibration range was generally 0.1 nM to 10 μM with R2>0.99 |
| Ion Mode: | POSITIVE |
| MS ID: | MS003946 |
| Analysis ID: | AN004199 |
| Instrument Name: | ABI Sciex 5500 QTrap |
| Instrument Type: | QTRAP |
| MS Type: | ESI |
| MS Comments: | Data analysis was performed using Analyst 1.5.2 software. Extracted ion chromatograms (EIC) corresponding to each metabolite were used for quantitation (MRM). The area under the curve of each EIC was normalized to that of the internal standard. For ceramides and sphingomyelins, the calibration range was generally 0.1 nM to 10 μM with R2>0.99 |
| Ion Mode: | POSITIVE |
