锌指核酸酶
清脆的
基因组编辑
转录激活物样效应核酸酶
核酸酶
电穿孔
Cas9
生物
基因组
效应器
基因组工程
回文
计算生物学
遗传学
分子生物学
DNA
细胞生物学
基因
出处
期刊:Methods in molecular biology
日期:2023-01-01
卷期号:: 125-134
被引量:1
标识
DOI:10.1007/978-1-0716-3016-7_10
摘要
Many genome-edited mouse and rat strains have been produced using engineered endonucleases, including zinc finger nuclease (ZFN), transcription activator-like effector nuclease (TALEN), or clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9. Especially, CRISPR-Cas9 is powerful tool that can be easy, rapid, and high-efficiency-produced new genome-edited strains. Furthermore, new technique, Technique for Animal Knockout system by Electroporation (TAKE), efficiently accelerate production of new strains by direct nuclease introduction into intact embryos using electroporation. This chapter presents a latest technical information in the production of genome-edited mouse and rat by TAKE method.
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