Cas9 (7A9-3A3) Mouse Monoclonal Antibody (Alexa Fluor^®594 Conjugate)#97534,Cell Signaling Technology (CST),97534

The CRISPR associated protein 9 (Cas9) is an RNA-guided DNA nuclease and part of theStreptococcus pyogenesCRISPR antiviral immunity system that provides adaptive immunity against extrachromosomal genetic material (1). The CRISPR antiviral mechanism of action involves three steps: (i), acquisition of foreign DNA by host bacterium; (ii), synthesis and maturation of CRISPR RNA (crRNA) followed by the formation of RNA-Cas nuclease protein complexes; and (iii), target interference through recognition of foreign DNA by the complex and its cleavage by Cas nuclease activity (2). The type II CRISPR/Cas antiviral immunity system provides a powerful tool for precise genome editing and has potential for specific gene regulation and therapeutic applications (3). The Cas9 protein and a guide RNA consisting of a fusion between a crRNA and a trans-activating crRNA (tracrRNA) must be introduced or expressed in a cell. A 20-nucleotide sequence at the 5' end of the guide RNA directs Cas9 to a specific DNA target site. As a result, Cas9 can be "programmed" to cut various DNA sites bothin vitroand in cells and organisms. CRISPR/Cas9 genome editing tools have been used in many organisms, including mouse and human cells (4,5). Research studies demonstrate that CRISPR can be used to generate mutant alleles or reporter genes in rodents and primate embryonic stem cells (6-8).Horvath, P. and Barrangou, R. (2010)Science327, 167-70.Wiedenheft, B. et al. (2012)Nature482, 331-8.Singh, P. et al. (2015)Genetics199, 1-15.Cong, L. et al. (2013)Science339, 819-23.Mali, P. et al. (2013)Science339, 823-6.Li, D. et al. (2013)Nat Biotechnol31, 681-3.Shen, B. et al. (2013)Cell Res23, 720-3.Niu, Y. et al. (2014)Cell156, 836-43.Alternate Namescas9; CRISPR-associated endonuclease Cas9/Csn1; csn1

cas9; CRISPR-associated endonuclease Cas9/Csn1; csn1