Powered by BiozThis cell line is a full mutation FXS iPS cell line that lacks FMR1 and FMRP expression consistent with FXS diagnosis.
- Cell Line Alias FX13-2
- Unit of Measure (UOM) Vial
- Cell Type Human iPS
- Sex Male
- Age at Collection 8 Years
- Reprogramming Method Viral transfection (Lentivirus: Oct4, Klf4, Sox2, cMyc)
- Disease Fragile X syndrome
- Genetic Alteration Mutation FMR1
- Pubmed Abstract Doers, ME et al. "iPSC-derived forebrain neurons from FXS individuals show defects in initial neurite outgrowth" Stem Cells Dev. 23.15 (2014) 1777-87
- Provider University of Wisconsin - Dr. Anita Bhattacharyya
- Collections Fragile X syndrome Collection
| Lot Number | Culture Platform | Lot Description | Banked By | Passage Number | Protocol | Product Information & Testing |
| WB68026 | mTeSR1/Matrigel | WiCell | 21 | WiCell Feeder Independent Pluripotent Stem Cell Protocol |
| Lot Number | Culture Platform | Lot Description | Banked By | Protocol | Product Information & Testing |
| WB66934 | TeSR-E8/Matrigel | WiCell | WiCell Feeder Independent Pluripotent Stem Cell Protocol |