CRISPR-Cas9 Antibody
Novus Biologicals, part of Bio-Techne | Catalog # NBP2-52717
Key Product Details
Validated by
Biological Validation
Species Reactivity
Bacteria
Applications
Immunoprecipitation, Western Blot
Label
Unconjugated
Antibody Source
Polyclonal Rabbit IgG
Concentration
1 mg/ml
Product Specifications
Immunogen
This CRISPR-Cas9 antibody was raised against CAS9 synthetic peptide within S. Pyogenes enzyme cas9 (Used in CRISPR/Cas9 Genome Editing system).
Clonality
Polyclonal
Host
Rabbit
Isotype
IgG
Theoretical MW
158.4 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Scientific Data Images for CRISPR-Cas9 Antibody
Western Blot: CRISPR-Cas9 Antibody [NBP2-52717]
Western Blot: CRISPR-Cas9 Antibody [NBP2-52717] - HEK293T were transfected with either WT CAS9 plasmid, CAS9 nickase plasmid or control vector. Equivalent amount of each cell lysates (10ug per lane) were immunoblotted with (1:2000). Theoretical molecular weight ~158 kDa.Western Blot: CRISPR-Cas9 Antibody [NBP2-52717]
Western Blot: CRISPR-Cas9 Antibody [NBP2-52717] - A. After the induction of CAS9 and XCAS9 in 293 cells with 2 ug/mL doxycycline for 3 days, CAS9 expression was accessed by WB. XCAS9 is a CAS9 variant with potentially higher fidelity and broader compatibility. B) The impact of expression levels of CAS9 on DNA DSB damage in hESCs. At the same lentiviral titers, the expression levels of CAS9 in hESCs transduced by standard lentiviral vector are higher than those transduced by the inducible lentiviral vector after 2 ug/mL Doxy treatment. Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/32170574) licensed under a CC-BY license.Immunoprecipitation: CRISPR-Cas9 Antibody [NBP2-52717]
Immunoprecipitation: CRISPR-Cas9 Antibody [NBP2-52717] - HEK293T were transfected with either WT CAS9 plasmid, CAS9 nickase plasmid (GE100019), or negative control vector (PS100001). Input: 10ug total cell lysates; WB was performed (1:2000). IP: 100ug of cell lysates were precipitated with 20ug of NBP2-52717 or control antibody, and 5ug Protein G Beads. Mouse anti-DDK monoclonal antibody was used in WB to detect the immuno-precipitated Cas9 (as Cas9 is Myc-DDK tagged)Applications for CRISPR-Cas9 Antibody
Application
Recommended Usage
Western Blot
1:500
Formulation, Preparation, and Storage
Purification
Immunogen affinity purified
Formulation
PBS (pH 7.3), 1.0% BSA and 50% Glycerol
Preservative
0.02% Sodium Azide
Concentration
1 mg/ml
Shipping
The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage
Store at -20C. Avoid freeze-thaw cycles.
Background: CRISPR-Cas9
Using CRISPR-Cas9 technology, double-stranded DNA breaks may be induced within specific targeted genome sequences (target DNA; protospacer) for insertion or removal of DNA sequences for gene editing applications. To target a specific loci, a gRNA that will bind to a specific target sequence of DNA within a genome is created. The gRNA will recognize the DNA sequence, and the Cas9 enzyme will cleave the DNA at the targeted location. Once the targeted DNA is removed by Cas9, the cell's own DNA repair mechanism is used to insert or remove a DNA sequence for genomic editing.
Cas9 detection is used to confirm and evaluate CRISPR Cas9 gRNA transfection efficiency. Western blot analysis of CRISPR-Cas9 gRNA transfected cell lysates with Cas9 antibodies identifies the protein having a theoretical molecular weight of 160kDa. Broad areas of research are benefiting from CRISPR-Cas9 based gene editing tools including studies of basic immunity functions, genetic screening and disease treatment (2). Ethical concerns have led to many countries making it illegal to manipulate human germline cells or perform embryo genome editing.
References
1. Oakes, B. L., Fellmann, C., Rishi, H., Taylor, K. L., Ren, S. M., Nadler, D. C., . . . Savage, D. F. (2019). CRISPR-Cas9 Circular Permutants as Programmable Scaffolds for Genome Modification. Cell, 176(1-2), 254-267.e216. doi:10.1016/j.cell.2018.11.052
2. Chiou, S. H., Winters, I. P., Wang, J., Naranjo, S., Dudgeon, C., Tamburini, F. B., . . . Winslow, M. M. (2015). Pancreatic cancer modeling using retrograde viral vector delivery and in vivo CRISPR/Cas9-mediated somatic genome editing. Genes Dev, 29(14), 1576-1585. doi:10.1101/gad.264861.115
Long Name
CRISPR-associated Protein 9
Alternate Names
Cas9, CRISPR-associated endonuclease Cas9/Csn1, CRISPR-Cas9/Csn1, CRISPR/Cas9, csn1, SPy_1046, SPy1046, SpyCas9, CRISPR-associated protein 9 nuclease
Additional CRISPR-Cas9 Products
Product Documents for CRISPR-Cas9 Antibody
Product Specific Notices for CRISPR-Cas9 Antibody
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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