Return to study ST002389 main page
MB Sample ID: SA238067
| Local Sample ID: | blank_3_Gln |
| Subject ID: | SU002478 |
| Subject Type: | Cultured cells |
| Subject Species: | Homo sapiens |
| Taxonomy ID: | 9606 |
| Gender: | Male and female |
| Cell Biosource Or Supplier: | ForIPS consortium |
| Cell Strain Details: | Midbrain neuronal precursor cells differentiated from patient derived induced pluripotent stem cells |
Select appropriate tab below to view additional metadata details:
Combined analysis:
| Analysis ID | AN003893 |
|---|---|
| Analysis type | MS |
| Chromatography type | GC |
| Chromatography system | Agilent 7890B gas chromatograph |
| Column | 30 m DB-35 ms and 5 m Duruguard capillary column |
| MS Type | EI |
| MS instrument type | Single quadrupole |
| MS instrument name | Agilent 5977 |
| Ion Mode | POSITIVE |
| Units | Mass isotopomer distributions |
MS:
| MS ID: | MS003633 |
| Analysis ID: | AN003893 |
| Instrument Name: | Agilent 5977 |
| Instrument Type: | Single quadrupole |
| MS Type: | EI |
| MS Comments: | One microliter sample was injected into an SSL injector at 270 °C in a split or splitless mode. GC-MS analysis was performed using an Agilent 7890B gas chromatograph equipped with a 30 m DB-35 ms and 5 m Duruguard capillary column. Metabolites were detected in selected ion mode by an Agilent 5977 MSD system. The MetaboliteDetector software was used to analyze chromatograms, calculate mass isotopomer distributions (MIDs) and perform relative comparison of metabolite levels. |
| Ion Mode: | POSITIVE |
