Advantage of delivering the gene therapy tool (Cas9) as purified protein formulation
Gene editing permits the alteration of genomic sequences in vitro and in vivo, which could serve as a powerful tool in basic research and human gene therapy. The recent clustered regularly interspaced short palindromic repeat (CRISPR) system has revolutionized the way of gene editing. To be used i...
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| Format: | Article |
| Language: | English |
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OMICS International
2017
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| Online Access: | http://irep.iium.edu.my/60039/ http://irep.iium.edu.my/60039/ http://irep.iium.edu.my/60039/1/advantage-of-delivering-the-gene-therapy-tool-cas9-as-purified-protein-formulation.pdf |