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 AAV-DJ is a synthetic serotype made from DNA family shuffling of 8 wild type serotypes of AAV, including AAV2, 4, 5, 8, 9, avian, bovine and goat AAV. This synthetic serotype has better infection efficiency in most cultured cells than wild type AAV serotype 1-8, and it also has superior liver & neuronal tropism for in vivo infection. This is an AAV-DJ expressing spCas9 nuclease under a short CMV7 promoter. It can be used along with guided RNA for targeted genome-editing. We can also package this spCas9 into other serotypes of AAV upon request.
Categories
AAV, Over-Expression, CRISPR/Cas9
Product Type
Pre-Made
Virus Type
AAV
Function
CRISPR/Cas9
Promoter
CMV7 (ubiquitous)
Storage Buffer
PBS/5% Glycerol
Viral Backbone
Recombinant AAV
Shelf Life
12 Months
HS Code
3822190000
UNSPSC Code
41106621
Insert Gene
spCas9
Serotype
AAV2//DJ
Availability
Ready to Ship
Titer
1x10^13 GC/ml
ITRs
AAV2
Reviews of CRISPR/spCas9 nuclease AAV AAV (AAV/DJ-CMV-spCas9)