Powered by BiozThis cell line is a modified version of WA01 (H1), engineered to contain the modified gene KCTD13.
- Unit of Measure (UOM) vial
- Cell Type Modified Human ES
- Sex Male
- Genetic Alteration Mutation Information Disruption of both alleles of KCTD13.
- Genetic Modification Keyword Isogenic; Autism
- Disease 16p11.2 disorders
- Genetic Alteration Mutation KCTD13
- Pubmed Abstract Martinez, RA et al. "Genome engineering of isogenic human ES cells to model autism disorders." Nucleic Acids Research 43(10) (2015).
- NIH Approval NIHhESC-10-0043
- Provider Allen Institute - Dr. Boaz Levi
- Collections Allen Institute Stem Cell Collection for Early Human Brain Development
| Lot Number | Culture Platform | Lot Description | Banked By | Passage Number | Protocol | Product Information & Testing |
| DB66695 | mTeSR1/Matrigel | Provider | 54 | WiCell Feeder Independent Pluripotent Stem Cell Protocol |