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WC019i-SMA-GM13

Cell Line Alias SMA-1
Cell Type Human iPS
Disease Spinal Muscular Atrophy (Type II)
Genetic Alteration/Mutation SMN1
Genetic Alteration/Mutation Information 3 copies of SMN2 gene with homozygous deletion of exons 7 and 8 in SMN1 gene
Sex Male
Age at Collection 3 Years
Ethnicity Caucasian
Genetically Related Cell Lines  
Reprogramming Method Viral transfection (Lentivirus: Oct4, Klf4, Sox2, cMyc)
Tissue Origin Skin Fibroblast (GM03813)
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
WB44684 mTeSR1/Matrigel   41 WiCell WiCell Feeder Independent Pluripotent Stem Cell Protocol PDF