JoVE Journal
Immunology and Infection
Immunology and Infection
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Lentiviral CRISPR/Cas9介导基因组编辑,用于疾病模型中造血细胞的研究
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Article
DOI:
10.3791/59977-v
•
08:14 min
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October 3rd, 2019
Lentiviral CRISPR/Cas9介导基因组编辑,用于疾病模型中造血细胞的研究
October 3rd, 2019
•
Chapters
Summary
Please note that all translations are automatically generated.
Click here for the English version.
本文介绍了CRISPR/Cas9系统对鼠血干细胞和祖细胞(HSPC)进行高效基因组编辑的协议,以快速开发具有造血系统特异性基因修饰的小鼠模型系统。