SAB4200751
Anti-CRISPR/Cas9 (C-terminal) antibody, Mouse monoclonal
clone 10C11-A12, purified from hybridoma cell culture
Synonym(s):
Anti-CRISPR-associated protein-9 nuclease, Anti-Crispr, Anti-Crsipr RNA
About This Item
antibody form
purified from hybridoma cell culture
Quality Level
antibody product type
primary antibodies
clone
10C11-A12, monoclonal
form
buffered aqueous solution
concentration
~1.00 mg/mL
technique(s)
immunoblotting: 1-2 μg/mL using whole extracts of human HEK-293T cells over-expressing CAS9 protein
immunofluorescence: 1.25-2.5 μg/mL using human HEK-293T cells over-expressing CAS9 protein
immunoprecipitation (IP): 5-10 μg/test using whole extract of human HEK-293T cells over-expressing CAS9 protein
UniProt accession no.
shipped in
dry ice
storage temp.
−20°C
target post-translational modification
unmodified
General description
The Cas9 endonuclease can be engineered with a single gRNA, directing a DNA double-strand break (DSB) at a desired genomic location. Similar to DSBs induced by zinc finger nucleases (ZFNs), the cell then activates endogenous DNA repair processes, either non-homologous end joining (NHEJ) or homology-directed repair (HDR), to heal the targeted DSB.
In comparison to other genome-editing technologies such as designer zinc fingers (ZFs), transcription activator–like effectors (TALEs) and homing meganucleases, the CRISPR/CAS9 system is a scalable, affordable and easy to engineer. Therefore, the anti-CRISPR/CAS9 antibody can be a useful tool for detecting CRISPR/CAS9 positively transfected cells, revealing DSB sites in the genome and in ChIP (Chromatin Immunoprecipitation) related assays
Immunogen
Application
Biochem/physiol Actions
Physical form
Storage and Stability
Other Notes
In order to obtain best results in different techniques and preparations we recommend determining optimal working concentration by titration test.
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Storage Class Code
10 - Combustible liquids
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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