SAB4200735
Anti-CRISPR/CAS9 -FITC antibody, Mouse monoclonal
clone 7A9-3A3, purified from hybridoma cell culture
Synonym(s):
Anti-CRISPR-associated protein-9 nuclease, Anti-Crispr, Anti-Crispr RNA
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conjugate
FITC conjugate
Quality Level
antibody form
purified from hybridoma cell culture
antibody product type
primary antibodies
clone
7A9-3A3, monoclonal
form
buffered aqueous solution
storage condition
protect from light
concentration
~1.0 mg/mL
technique(s)
immunofluorescence: 1:200-1:400 using human HEK-293T cells over-expressing CAS9 protein
isotype
IgG1
UniProt accession no.
shipped in
dry ice
storage temp.
−20°C
target post-translational modification
unmodified
1 of 4
This Item | SAB4200756 | SAB4200777 | MABS1291 |
|---|---|---|---|
| clone 7A9-3A3, monoclonal | clone AsCpf-11, monoclonal | clone LbCpf1, monoclonal | clone 10C11-A12, monoclonal |
| conjugate FITC conjugate | conjugate - | conjugate - | conjugate - |
| antibody form purified from hybridoma cell culture | antibody form purified from hybridoma cell culture | antibody form purified from hybridoma cell culture | antibody form purified antibody |
| storage temp. −20°C | storage temp. −20°C | storage temp. −20°C | storage temp. - |
| UniProt accession no. | UniProt accession no. | UniProt accession no. | UniProt accession no. |
| technique(s) immunofluorescence: 1:200-1:400 using human HEK-293T cells over-expressing CAS9 protein | technique(s) immunoblotting: 1.25-2.5 μg/mL using purified recombinant AsCpf1 produced in E. coli, immunofluorescence: 1.25-2.5 μg/mL using human HEK-293T cells over-expressing AsCpf1 protein, immunoprecipitation (IP): 2.5-5 μg/test using lysate of human HEK-293T cells over-expressing AsCpf1 protein | technique(s) immunoblotting: 0.6-1.2 μg/mL using human HEK-293T cells over-expressing LbCpf1 protein, immunofluorescence: 0.25-0.5 μg/mL using human HEK-293T cells over-expressing LbCpf1 protein, immunoprecipitation (IP): 1-2.5 μg/test using lysate of human HEK-293T cells over-expressing LbCpf1 protein | technique(s) immunocytochemistry: suitable, immunoprecipitation (IP): suitable, western blot: suitable |
General description
The type II CRISPR/Cas system has been adapted to expression in eukaryotic cells. The Cas9 endonuclease can be engineered with a single gRNA (guide RNA), directing a DNA double-strand break (DSB) at a desired genomic location. As a result, the cell activates endogenous DNA repair processes, either non-homologous end joining (NHEJ) or homology-directed repair (HDR). 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-FITC conjugated antibody can be a useful tool for detecting CRISPR/CAS9 positively transfected cells, revealing DSB sites in their genome.
Immunogen
Application
Physical form
Preparation Note
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
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