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WC007i-FX13-2

This 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
Cell Type Human iPS
Disease Fragile X syndrome
Genetic Alteration/Mutation FMR1
Sex Male
Age at Collection 8 Years
Genetically Related Cell Lines  
Reprogramming Method Viral transfection (Lentivirus: Oct4, Klf4, Sox2, cMyc)
Provider University of Wisconsin - Dr. Anita Bhattacharyya
dbGaP Data  
hPSCReg ID  
NIH Approval  
Pub Med Abstract  
Collection(s) Fragile X syndrome Collection
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Current Lot Information

Lot Number Culture Platform Lot Description Passage Number Banked By Protocol Product Information & Testing
WB68026 mTeSR1/Matrigel   21 WiCell WiCell Feeder Independent Pluripotent Stem Cell Protocol PDF

Historical Lot Information

Lot Number Culture Platform Lot Description Banked By Protocol Product Information & Testing
WB66934 TeSR-E8/Matrigel   WiCell WiCell Feeder Independent Pluripotent Stem Cell Protocol PDF