- Cell Line Alias SMA-2
- Unit of Measure (UOM) vial
- Cell Type Human iPS
- Sex Male
- Age at Collection 2 Years
- Reprogramming Method Viral transfection (Lentivirus: Oct4, Klf4, Sox2, cMyc)
- Tissue Origin Lens Fibroblast (GM09677)
- Genetic Alteration Mutation Information 3 copies of SMN2 gene with homozygous deletion of exons 7 and 8 in SMN1 gene
- Disease Spinal Muscular Atrophy (Type I)
- Ethnicity Caucasian
- Genetic Alteration Mutation SMN1
- Pubmed Abstract Liu, H. et al. "Spinal muscular atrophy patient-derived motor neurons exhibit hyperexcitability." Sci. Rep. (2015) 20;5:12189.
- Provider University of Wisconsin - Dr. Su-Chun Zhang
- Collections Spinal Muscular Atrophy Collection
Lot Number | Culture Platform | Lot Description | Banked By | Passage Number | Protocol | Product Info URL |
WB47072 | mTeSR1/Matrigel | WiCell | 11 | WiCell Feeder Independent Pluripotent Stem Cell Protocol |