| Literature DB >> 25762293 |
Rahel Wettstein1, Maxime Bodak1, Constance Ciaudo2.
Abstract
CRISPR/Cas9, originally discovered as a bacterial immune system, has recently been engineered into the latest tool to successfully introduce site-specific mutations in a variety of different organisms. Composed only of the Cas9 protein as well as one engineered guide RNA for its functionality, this system is much less complex in its setup and easier to handle than other guided nucleases such as Zinc-finger nucleases or TALENs.Here, we describe the simultaneous transfection of two paired CRISPR sgRNAs-Cas9 plasmids, in mouse embryonic stem cells (mESCs), resulting in the knockout of the selected target gene. Together with a four primer-evaluation system, it poses an efficient way to generate new independent knockout mouse embryonic stem cell lines.Entities:
Keywords: (Homozygous) knockout; CRISPR-Cas9 paired design; CRISPR/Cas9; Genome engineering; mESCs: mouse embryonic stem cells
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Year: 2016 PMID: 25762293 DOI: 10.1007/7651_2015_213
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745