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Author Spotlight: Efficient CRISPR/Cas9 Genome Editing in Bone Marrow-Derived Macrophages for Precise Gene Disruption
用于小鼠骨髓来源巨噬细胞基因组编辑的电穿孔和核糖核蛋白递送的制备
该协议描述了使用 体外 组装并通过电穿孔递送的Cas9-sgRNA核糖核蛋白复合物在小鼠骨髓来源的巨噬细胞中进行基因组编辑的过程。
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