“CRISPR-Cas9 Specificity: Taming Off-target Mutagenesis” Technical bulletin

The CRISPR (Clustered, Regularly Interspaced, Short Palindromic Repeats)-Cas (CRISPR-associated) (CRISPR-Cas) system has become trendy as it is suitable for numerous applications such as gene knockouts, genome-engineering, to name but a few. In a recent Technical Bulletin, Ed Davis describes the mechanism of CRISPR-Cas for genome editing and how the recent experimental improvements improve CRISPR-Cas9 specificity while reducing off-target effects.

In this Bulletin, Ed Davis and GeneCopoeia’s experts demonstrate how recent improvements in sgRNA design and strategy, combined with alternative versions of the Cas9 nuclease, make CRISPR-Cas9 CRISPR-Cas 9 Genome Engineeringa viable approach for many applications, including gene therapy, with much less concern about off-target mutagenesis than initially thought.

See how these experts are able to design a full suite of efficient and specific CRISPR-Cas9 genome editing tools, including both the wild-type and D10A nickase versions of Cas9, sgRNA design for single and double nickase targets and sgRNA and Cas9 vectors in both lentiviral and non-viral formats

Request for your free copy of the Technical Bulletin “CRISPR-Cas9 Specificity: Taming Off-target Mutagenesis” now!

 

 

 

 

Trackbacks

  1. […] Davis (from GeneCopoeia) “CRISPR-Cas9 Specificity: Taming Off-target Mutagenesis” (2014) Technical bulletin -TNGE2-050814 (Mechanism of CRISPR for genome editing and experimental […]

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