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WC023i-SMA-GM232

Cell Line Alias SMA-3
Cell Type Human iPS
Disease Spinal Muscular Atrophy (Type I)
Genetic Alteration/Mutation SMN1
Genetic Alteration/Mutation Information 2 copies of the SMN2 gene and is homozygous for deletion of exons 7 and 8 of the SMN1 gene
Sex Male
Age at Collection 7 Months
Ethnicity Caucasian
Genetically Related Cell Lines  
Reprogramming Method Viral transfection (Lentivirus: Oct4, Klf4, Sox2, cMyc)
Tissue Origin Fibroblast (GM00232)
Provider University of Wisconsin - Dr. Su-Chun Zhang
dbGaP Data  
hPSCReg ID  
NIH Approval  
Pub Med Abstract  
Collection(s) Spinal Muscular Atrophy Collection
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Current Lot Information

Lot Number Culture Platform Lot Description Passage Number Banked By Protocol Product Information & Testing
WB47173 mTeSR1/Matrigel   33 WiCell WiCell Feeder Independent Pluripotent Stem Cell Protocol PDF