Generation of SCN1A Knock out induced pluripotent stem cell (iPSC) line
Summary
The SCN1A gene encodes the voltage-gated Na+ channel alpha subunit Nav1.1 and is the most clinically relevant epilepsy gene. Variants in SCN1A result in a broad phenotypic spectrum of epilepsy syndromes, from mild genetic epilepsy with febrile seizures plus to severe Dravet syndrome (DS). Here, we generated a SCN1A-knockout human iPSC line via CRISPR/Cas9 gene editing. The resulting iPSCs had a normal karyotype, were free of genomically integrated epitomal plasmids, expressed pluripotency markers, and maintained trilineage differentiation potential. Copyright © 2021 The Author(s). Published by Elsevier B.V. All rights reserved.
Authors | Shan W, Yang X, Ren Q, Wang Q |
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Journal | Stem cell research |
Publication Date | 2021 Aug;55:102452 |
PubMed | 34247112 |
DOI | 10.1016/j.scr.2021.102452 |