Powered by BiozThis cell line contains an expected karyotypic abnormality consistent with the phenotype indicated in the “disease” field below. Please see the karyotype report in the “Product Information & Testing” PDF(s) linked below for more information.
- Cell Line Alias HE00812
- Unit of Measure (UOM) vial
- Cell Type Human iPS
- Sex Female
- Age at Collection 86 Years
- Ethnicity Information Ethnicity was obtained by sequencing.
- Reprogramming Method Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, L-Myc, shp53, Lin28)
- Tissue Origin Blood
- Genetic Alteration Mutation Information Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the risk alleles at all 3 sites.
- Disease Turner Syndrome
- Ethnicity Caucasian
- Provider The Scripps Research Institute - Dr. Eric Topol
- Collections NHLBI Next Gen - Coronary artery disease and myocardial infarction (Dr. Eric Topol, Scripps Research Institute), Wellderly Study Collection
| Lot Number | Culture Platform | Lot Description | Banked By | Passage Number | Protocol | Product Info URL |
| DB43120 | mTeSR1/Matrigel | Provider | 10 | WiCell Feeder Independent Pluripotent Stem Cell Protocol |