清脆的
Cas9
电穿孔
诱导多能干细胞
基因组编辑
生物
人诱导多能干细胞
荧光蛋白
细胞生物学
计算生物学
基因敲除
胚胎干细胞
分子生物学
绿色荧光蛋白
遗传学
基因
作者
Tatsuya Anzai,Hiromasa Hara,Nawin Chanthra,Taketaro Sadahiro,Masaki Ieda,Yutaka Hanazono,Hideki Uosaki
标识
DOI:10.1007/978-1-0716-1484-6_22
摘要
A knock-in can generate fluorescent or Cre-reporter under the control of an endogenous promoter. It also generates knock-out or tagged-protein with fluorescent protein and short tags for tracking and purification. Recent advances in genome editing with clustered regularly interspaced short palindromic repeat (CRISPR) and CRISPR-associated protein 9 (Cas9) significantly increased the efficiencies of making knock-in cells. Here we describe the detailed protocols of generating knock-in mouse and human pluripotent stem cells (PSCs) by electroporation and lipofection, respectively.
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