phex2 gus vector (Addgene inc)
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85
Structured Review
Addgene inc
phex2 gus vector
Phex2 Gus Vector, supplied by Addgene inc, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/phex2+gus+vector/pHEX2+GUS+(Plasmid+%2344462)/pm23625357-72-1-4
Average 85 stars, based on 1 article reviews
Phex2 Gus Vector, supplied by Addgene inc, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/phex2+gus+vector/pHEX2+GUS+(Plasmid+%2344462)/pm23625357-72-1-4
Average 85 stars, based on 1 article reviews
phex2 gus vector - by Bioz Stars,
2026-10
85/100 stars
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Plasmid Preparation:Article Title: A rapid assay to quantify the cleavage efficiency of custom-designed nucleases in planta. Article Snippet: Custom-designed nucleases are a promising technology for genome editing through the catalysis of double-strand DNA breaks within target loci and subsequent repair by the host cell, which can result in targeted mutagenesis or gene replacement.. Implementing this new technology requires a rapid means to determine the cleavage efficiency of these custom-designed proteins in planta.. Here we present such an assay that is based on cleavage-dependent luciferase gene correction as part of a transient dual-luciferase reporter (Promega) expression system. Control:Article Title: A rapid assay to quantify the cleavage efficiency of custom-designed nucleases in planta. Article Snippet: Custom-designed nucleases are a promising technology for genome editing through the catalysis of double-strand DNA breaks within target loci and subsequent repair by the host cell, which can result in targeted mutagenesis or gene replacement.. Implementing this new technology requires a rapid means to determine the cleavage efficiency of these custom-designed proteins in planta.. Here we present such an assay that is based on cleavage-dependent luciferase gene correction as part of a transient dual-luciferase reporter (Promega) expression system. Expressing:Article Title: A rapid assay to quantify the cleavage efficiency of custom-designed nucleases in planta. Article Snippet: Custom-designed nucleases are a promising technology for genome editing through the catalysis of double-strand DNA breaks within target loci and subsequent repair by the host cell, which can result in targeted mutagenesis or gene replacement.. Implementing this new technology requires a rapid means to determine the cleavage efficiency of these custom-designed proteins in planta.. Here we present such an assay that is based on cleavage-dependent luciferase gene correction as part of a transient dual-luciferase reporter (Promega) expression system. Activity Assay:Article Title: A rapid assay to quantify the cleavage efficiency of custom-designed nucleases in planta. Article Snippet: Custom-designed nucleases are a promising technology for genome editing through the catalysis of double-strand DNA breaks within target loci and subsequent repair by the host cell, which can result in targeted mutagenesis or gene replacement.. Implementing this new technology requires a rapid means to determine the cleavage efficiency of these custom-designed proteins in planta.. Here we present such an assay that is based on cleavage-dependent luciferase gene correction as part of a transient dual-luciferase reporter (Promega) expression system. |