| Literature DB >> 34302663 |
Tatsuya Anzai1,2, Hiromasa Hara1,3, Nawin Chanthra1, Taketaro Sadahiro4, Masaki Ieda4, Yutaka Hanazono1,5, Hideki Uosaki6,7.
Abstract
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.Entities:
Keywords: CRISPR-Cas9; Genome editing; Homology-directed repair; Knock-in; Pluripotent stem cells
Year: 2021 PMID: 34302663 DOI: 10.1007/978-1-0716-1484-6_22
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745