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Efficient generation of mice carrying homozygous double-floxp alleles using the Cas9-Avidin/Biotin-donor DNA system

The clustered, regularly interspaced, short palin- dromic repeats (CRISPR)/CRISPR-associated protein 9 (Casg) system is a versatile tool for genomic engineering in mammalian cells and organisms, enabling the intro- duction of site-specific genomic double-strand breaks (DSBs) [1]. The resulting DSBs...

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Bibliographic Details
Published in:Cell research 2017-04, Vol.27 (4), p.578-581
Main Authors: Ma, Ming, Zhuang, Fengfeng, Hu, Xiongbing, Wang, Bolun, Wen, Xian-Zi, Ji, Jia-Fu, Xi, Jianzhong Jeff
Format: Article
Language:English
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Summary:The clustered, regularly interspaced, short palin- dromic repeats (CRISPR)/CRISPR-associated protein 9 (Casg) system is a versatile tool for genomic engineering in mammalian cells and organisms, enabling the intro- duction of site-specific genomic double-strand breaks (DSBs) [1]. The resulting DSBs are repaired by at least two distinct and competitive mechanisms, nonhomolo- gous end-joining (NHEJ) and homology-directed repair (HDR). The former results in insertions and deletions (indels), whereas the latter leads to precise genetic modi- fication.
ISSN:1001-0602
1748-7838
DOI:10.1038/cr.2017.29