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...
Main Author: | Doolaanea, Abd Almonem |
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Format: | Article |
Language: | English |
Published: |
OMICS International
2017
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Subjects: | |
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 |
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