CRISPR-Cas9 genome editing of immune cell types holds great therapeutic potential, but application of genome editing to primary human immune cells has been hampered by challenges in efficient delivery and expression of the CRISPR machinery. Explore our protocols and resources for information on how to overcome these barriers and perform high-efficiency genome editing of these difficult-to-manipulate cell types in your own lab.
For detailed protocols developed specifically for our products, please consult the Product Information Sheet or enter the product keyword or catalog number below.
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