摘要
The clustered regularly interspaced short palindromic repeat （CRISPR） - CRISPR-associated protein 9 （CRISPR-Cas9） system has emerged as a versatile molecular tool for genome editing in various organisms in recent years （Tsai and Joung, 2016）. In this system, the endonuclease of Cas9 is directed to DNA targets by a synthetic guide RNA （sgRNA）.
The clustered regularly interspaced short palindromic repeat （CRISPR） - CRISPR-associated protein 9 （CRISPR-Cas9） system has emerged as a versatile molecular tool for genome editing in various organisms in recent years （Tsai and Joung, 2016）. In this system, the endonuclease of Cas9 is directed to DNA targets by a synthetic guide RNA （sgRNA）.
