Abstract
CRISPR/Cas9 is a novel method that has become the most widely used genome editing technology around the world. Its widespread adoption is largely due to its simplicity and easy of use. Here, we introduce the construction of vectors and genome editing of the target gene in cells expressing the CRISPR/Cas9 system.
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APA
Hatada, I., & Horii, T. (2017). CRISPR/Cas9. In Methods in Molecular Biology (Vol. 1630, pp. 37–42). Humana Press Inc. https://doi.org/10.1007/978-1-4939-7128-2_3
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