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- Cell Type Human iPS
- Sex Male
- Age at Collection 29 Years
- Reprogramming Method Transfection with a combination of pEP4EO2SET2K, pEP4EO2SEN2K and pCEP-M2L plasmids
- Tissue Origin Blood (GM20920)
- Genetic Alteration Mutation Information Mutation of A>T in the b-globin (HBB) gene that changes codon 6 from Glu (GAG) to Val (GTG)
- Diagnosis Information Diagnosis of Sickle Cell Anemia was physician reported. Age of diagnosis was 6 months. Age of onset was 18 months.
- Disease Sickle cell anemia SS
- Ethnicity African American > Nigerian
- Genetic Alteration Mutation HBB
- Provider University of Wisconsin - Dr. Igor Slukvin
- Collections Uncategorized
| Lot Number | Culture Platform | Lot Description | Banked By | Passage Number | Protocol | Product Info URL |
| WB66718 | mTeSR1/Matrigel | WiCell | 19 | WiCell Feeder Independent Pluripotent Stem Cell Protocol |