codon-optimized cas9 Search Results


seeds of maize  (Jinsheng Group Co Ltd)
90
Jinsheng Group Co Ltd seeds of maize
Seeds Of Maize, supplied by Jinsheng Group Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/seeds of maize/product/Jinsheng Group Co Ltd
Average 90 stars, based on 1 article reviews
seeds of maize - by Bioz Stars, 2026-05
90/100 stars
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human codon-optimized cas9  (Darma Inc)
90
Darma Inc human codon-optimized cas9
Schematic illustration of <t>Cas9/gRNA</t> genome editing. a sgRNA-mediated <t>Cas9</t> <t>protein</t> can bind to target sequences of site and cut DNA double strands. b When the DNA double-strand breaks occur, the cell initiates the self-repair mechanism. The NHEJ-dominated repair pathway will cause the random loss, insertion, and replacement of bases at the breakage point, resulting in gene mutation. The HR pathway will accurately edit the target gene guided by the donor DNA fragment. c Single-promoter-driven gRNA expression cassette. d multiple gRNA expression cassettes can be constructed by concatenating 2 or more of gRNA linked together by linkers, which can then be enzymatically processed into multiple single gRNAs thus targeting multiple sites
Human Codon Optimized Cas9, supplied by Darma Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human codon-optimized cas9/product/Darma Inc
Average 90 stars, based on 1 article reviews
human codon-optimized cas9 - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier
yeast codon optimized cas9 28  (Twist Bioscience)
86
Twist Bioscience yeast codon optimized cas9 28
Schematic illustration of <t>Cas9/gRNA</t> genome editing. a sgRNA-mediated <t>Cas9</t> <t>protein</t> can bind to target sequences of site and cut DNA double strands. b When the DNA double-strand breaks occur, the cell initiates the self-repair mechanism. The NHEJ-dominated repair pathway will cause the random loss, insertion, and replacement of bases at the breakage point, resulting in gene mutation. The HR pathway will accurately edit the target gene guided by the donor DNA fragment. c Single-promoter-driven gRNA expression cassette. d multiple gRNA expression cassettes can be constructed by concatenating 2 or more of gRNA linked together by linkers, which can then be enzymatically processed into multiple single gRNAs thus targeting multiple sites
Yeast Codon Optimized Cas9 28, supplied by Twist Bioscience, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/yeast codon optimized cas9 28/product/Twist Bioscience
Average 86 stars, based on 1 article reviews
yeast codon optimized cas9 28 - by Bioz Stars, 2026-05
86/100 stars
  Buy from Supplier

Image Search Results


Schematic illustration of Cas9/gRNA genome editing. a sgRNA-mediated Cas9 protein can bind to target sequences of site and cut DNA double strands. b When the DNA double-strand breaks occur, the cell initiates the self-repair mechanism. The NHEJ-dominated repair pathway will cause the random loss, insertion, and replacement of bases at the breakage point, resulting in gene mutation. The HR pathway will accurately edit the target gene guided by the donor DNA fragment. c Single-promoter-driven gRNA expression cassette. d multiple gRNA expression cassettes can be constructed by concatenating 2 or more of gRNA linked together by linkers, which can then be enzymatically processed into multiple single gRNAs thus targeting multiple sites

Journal: Applied Microbiology and Biotechnology

Article Title: CRISPR/Cas9 genome editing technology in filamentous fungi: progress and perspective

doi: 10.1007/s00253-019-10007-w

Figure Lengend Snippet: Schematic illustration of Cas9/gRNA genome editing. a sgRNA-mediated Cas9 protein can bind to target sequences of site and cut DNA double strands. b When the DNA double-strand breaks occur, the cell initiates the self-repair mechanism. The NHEJ-dominated repair pathway will cause the random loss, insertion, and replacement of bases at the breakage point, resulting in gene mutation. The HR pathway will accurately edit the target gene guided by the donor DNA fragment. c Single-promoter-driven gRNA expression cassette. d multiple gRNA expression cassettes can be constructed by concatenating 2 or more of gRNA linked together by linkers, which can then be enzymatically processed into multiple single gRNAs thus targeting multiple sites

Article Snippet: L. maculans , Human codon-optimized Cas9, hph , act1 , AMT , NHEJ , Double-gene disruption , Darma et al. .

Techniques: Mutagenesis, Expressing, Construct

The history of the development and application of CRISPR/Cas9 technology in filamentous fungi; different colors represent different promoter-driven gRNA expression cassettes

Journal: Applied Microbiology and Biotechnology

Article Title: CRISPR/Cas9 genome editing technology in filamentous fungi: progress and perspective

doi: 10.1007/s00253-019-10007-w

Figure Lengend Snippet: The history of the development and application of CRISPR/Cas9 technology in filamentous fungi; different colors represent different promoter-driven gRNA expression cassettes

Article Snippet: L. maculans , Human codon-optimized Cas9, hph , act1 , AMT , NHEJ , Double-gene disruption , Darma et al. .

Techniques: CRISPR, Expressing

The application of the CRISPR/Cas9 system in filamentous fungi

Journal: Applied Microbiology and Biotechnology

Article Title: CRISPR/Cas9 genome editing technology in filamentous fungi: progress and perspective

doi: 10.1007/s00253-019-10007-w

Figure Lengend Snippet: The application of the CRISPR/Cas9 system in filamentous fungi

Article Snippet: L. maculans , Human codon-optimized Cas9, hph , act1 , AMT , NHEJ , Double-gene disruption , Darma et al. .

Techniques: CRISPR, Expressing, Selection, Marker, Disruption, Modification, Electroporation