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AI09e-KCTD13a

This cell line is a modified version of WA01 (H1), engineered to contain the modified gene KCTD13.
Cell Type Modified Human ES
Disease 16p11.2 disorders
Genetic Alteration/Mutation KCTD13
Genetic Alteration/Mutation Information Disruption of one allele of KCTD13.
Genetic Modification Keyword Isogenic; Autism
Sex Male
Genetically Related Cell Lines  
Provider Allen Institute - Dr. Boaz Levi
dbGaP Data  
hPSCReg ID  
NIH Approval  
Pub Med Abstract  
Related Products
Collection(s) Allen Institute Stem Cell Collection for Early Human Brain Development
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Current Lot Information

Lot Number Culture Platform Lot Description Passage Number Banked By Protocol Product Information & Testing
DB66694 mTeSR1/Matrigel   55 Provider WiCell Feeder Independent Pluripotent Stem Cell Protocol PDF