清脆的
电穿孔
转染
Cas9
基因敲除
基因组编辑
计算生物学
生物
基因
功能(生物学)
遗传学
标识
DOI:10.1007/978-1-4939-9740-4_9
摘要
CRISPR-Cas9 is a unique technology that enables geneticists and medical researchers to edit genomic DNA for studying biology, pathogenesis, and molecular basis of treatment in malignant B cells. Unfortunately, malignant B cells are extremely difficult to transfect by most traditional methods. In this chapter, we describe the use of the Nucleofector™ Technology-based electroporation system with optimized transfection conditions for generating a malignant B cell model, JEKO-1, with ROR1-gene knockout via CRISPR-Cas9 technology.
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