AAV-ESYN-SACAS9

Vector Biolabs

AAV-ESYN-SACAS9

5

Other Application

Research Use Only

1E13 GC/ml

Cas9 is the nuclease guided by the crRNA and tracrRNA (or trans-activating crRNA) to cleave specific DNA sequences. A guide RNA (gRNA) can be designed to include a hairpin that mimics the tracrRNA-crRNA complex. Binding specificity is based on the gRNA and a three nucleotide NGG sequence called the protospacer adjacent motif (PAM) sequence. With its ease in designing guide sequences to target specific genomic loci, the CRISPR/Cas system is a much simpler, faster, and robust alternative to TALEN and Zinc finger nuclease platforms. The Cas9 from Streptococcus pyogenes SF370 (SpCas9) is too big to be packaged into AAV for most promoters, and theres no extra room for including a sgRNA in the same payload with spCas9 in AAV. A small Cas9 from Staphylococcus aureus subsp. aureus (SaCas9) with high efficiency for cleaving mammalian endogenous DNA is the ideal solution to package into AAV along with sgRNA for effective gene modification in vivo. This is an AAV-DJ (a synthetic serotype made from 8 wild type AAV including AAV2, 4, 5, 8, 9) expressing saCas9 nuclease under a neuronal specific eSYN promoter. The eSYN is a hybrid promoter consisting of a 0.4Kb CMV enhancer (e) and the 0.45Kb human Synapsin I promoter fragment (SYN). eSYN promoter provides 2-4 fold higher expression than that of the parental hSYN1 promoter. This AAV-eSYN-saCas9 can be package into other AAV serotypes upon request.

-80°C

41106621