Each CRISPR/Cas9 Knockout (KO) Plasmid product consists of a pool of 3 plasmids designed to ensure identification and cleavage of a specific gene for maximum knockout efficiency. Each plasmid encodes a unique 20 nt sequence derived from the GeCKO (v2) library.
Each CRISPR/Cas9 Knockout (KO) Plasmid product consists of a pool of 3 plasmids designed to ensure identification and cleavage of a specific gene for maximum knockout efficiency. Each plasmid encodes a unique 20 nt sequence derived from the GeCKO (v2) library.
CRISPR/Cas9 KO Plasmids consists of RACK1-specific 20 nt guide RNA sequences derived from the GeCKO (v2) library
For CRISPR gene knockout, gRNA sequences direct the Cas9 protein to induce a site-specific double strand break (DSB) in the genomic DNA
Target-specific CRISPR Plasmids for both gene knockout and activation are available. Please refer to the detailed product information in the tabs below
Gene knockdown or activation can be assayed using RACK1 Antibody (B-3): sc-17754
All products are provided as transfection-ready, purified plasmid DNA, except the Lentiviral Activation Particles which have been prepackaged as Lentiviral Particles for use with hard-to-transfect cells
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Ordering Information
Double Nickase Plasmids
Recommended Control Products
SEE ALSO...
RACK1 Antibodies for analysis of cellular responses to RACK1 CRISPR Products
CRISPR/Cas9 KO plasmids, Double Nickase Plasmids and CRISPR/dCas9 Activation plasmids are considered a "Licensed Product" and are to be used in accordance with the Limited/Label License. Click here for details
Description
20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
RACK1 Double Nickase Plasmid (m) consists of a pair of plasmids each encoding a D10A mutated Cas9 nuclease and a target-specific 20 nt guide RNA (gRNA) designed to knockout gene expression with greater specificity than its CRISPR/Cas9 KO counterpart
Paired gRNA sequences are offset by approximately 20 bp to allow for specific Cas9-mediated double nicking of the genomic DNA, which mimics a DSB
One plasmid in the pair contains a puromycin-resistance gene for selection; the other plasmid in the pair contains a GFP marker to visually confirm transfection
The paired gRNAs encoded by RACK1 Double Nickase Plasmid (m2) differ from the paired gRNAs in RACK1 Double Nickase Plasmid (m)
Following transfection, gene knockout efficiency can be assayed by WB, IF or IHC using antibody: RACK1 Antibody (B-3): sc-17754