Powered by Bioz** This cell line has an unexpected abnormal karyotype. Please see the karyotype report in the “Product Information & Testing” PDF(s) linked below for more information.
This cell line is a modified version of WIBR3, engineered to contain a DJ1 exon 1-5 deletion. Mutations in DJ1, encoding the Parkinson disease protein 7, have been identified as a rare cause of autosomal recessive Parkinson’s Disease (PD).
- Cell Line Alias WIBR3_DJ1_X1-5DEL_2876
- Unit of Measure (UOM) vial
- Cell Type Modified Human ES
- Sex Female
- Genetic Alteration Mutation Information DJ1 Ex 1-5 Deletion, NM_007262.5, c.-4252_322+1945del/c.-4245_322+1942del (NP_009193.2, no protein expected)
- Genetic Modification Keyword Isogenic - Parkinson's Disease
- Disease Parkinson's Disease
- Genetic Alteration Mutation DJ1
- hPSCReg ID WIBRe001-A-28
- Provider Albert Einstein College of Medicine
- Collections iSCORE-PD: Isogenic Stem Cell Collection to Research Parkinson’s Disease
| Lot Number | Culture Platform | Lot Description | Banked By | Passage Number | Protocol | Product Information & Testing |
| WB69034 | iSCORE 01 medium / 2x CF1 MEF | WiCell | 46 | WiCell Feeder Based (MEF) Protocol 01 for Culture of MJFF iSCORE Lines |