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Improved CRISPR/Cas9 gene editing by fluorescence activated cell sorting of green fluorescence protein tagged protoplasts.

BMC Biotechnol.. 2019; 
PetersenBent Larsen,M?llerSvenning Rune,MravecJozef,J?rgensenBodil,ChristensenMikkel,LiuYing,WandallHans H,BennettEric Paul,YangZ
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CRISPR Bacteria & Yeast Engineering The gRNA Gateway entry vector V26 (pUC57_attL1-AtU6:BbsI-BbsI-tracr-TT_AttL2) was synthesized by Genscript. Get A Quote

摘要

CRISPR/Cas9 is widely used for precise genetic editing in various organisms. CRISPR/Cas9 editing may in many plants be hampered by the presence of complex and high ploidy genomes and inefficient or poorly controlled delivery of the CRISPR/Cas9 components to gamete cells or cells with regenerative potential. Optimized strategies and methods to overcome these challenges are therefore in demand.

关键词

CRISPR/Cas9,Fluorescence activated cell sorting,Genome engineering,Mutation enrichment,Nicotiana benthamiana,Precise genetic editing,Protoplas