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Protocol for editing fibroblasts with in vitro transcribed Cas9 mRNA and profile off-target editing by optimized GUIDE-seq

Summary: CRISPR-Cas9 gene editing is an efficient technique to modify specific sites/regions of DNA. Delivery of the Cas9 by mRNA is particularly promising in pre-clinical genome editing applications for its transient, nonintegrating feature. However, the off-target of Cas9-gRNA still remains a conc...

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Bibliografiska uppgifter
Huvudupphov: Zhuokun Li, Ganna Reint, Emma Maria Haapaniemi
Materialtyp: Artigo
Språk:Inglês
Utgiven: Elsevier 2023-12-01
Serie:STAR Protocols
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Länkar:http://www.sciencedirect.com/science/article/pii/S2666166723006299
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