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JFRBi4

** The karyotype for this cell line may contain a non-clonal finding known to be recurrent in pluripotent stem cells. Please see the karyotype report in the currently distributing lot(s) Product Information & Testing PDF(s) linked below for more information.

Additional clones from this iPS cell line (JFRBi1, JFRBi2, JFRBi3 and JFRBi5) are available from WiCell.
Cell Line Alias 01457
Cell Type Human iPS
Disease Limb-Girdle Muscular Dystrophy, LGMD2B
Diagnosis Information Limb-Girdle Muscular Dystrophy, LGMD2B was physican reported. Age of onset (i.e. muscle weakness) 20 years.
Genetic Alteration/Mutation DYSF (heterozygous 2 mutations)
Genetic Alteration/Mutation Information c.5946+1G>Ac.5497G>T; p.Glu1833X
Sex Male
Age at Collection 48 Years
Ethnicity Caucasian
Genetically Related Cell Lines  
Reprogramming Method Non-integrating (OCT4, SOX2, NANOG, LIN28, L-MYC, KLF4, SV40LT)
Tissue Origin Blood
Provider Jain Foundation
dbGaP Data  
hPSCReg ID  
NIH Approval  
Pub Med Abstract  
Collection(s) Dysferlin-Deficient Collection
Have you received this cell line previously? Yes No Why we ask
Quantity: Learn about our volume discounts

Current Lot Information

Lot Number Culture Platform Lot Description Passage Number Banked By Protocol Product Information & Testing
WB66606 TeSR-E8/Matrigel   8 WiCell WiCell Feeder Independent Pluripotent Stem Cell Protocol PDF