Anti-CRISPR/Cas9 (Clone 7A9-3A3) – Purified No Carrier Protein
Anti-CRISPR/Cas9 (Clone 7A9-3A3) – Purified No Carrier Protein
Product No.: C3455
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Clone 7A9-3A3 Target CRISPR/Cas9 Formats AvailableView All Product Type Hybridoma Monoclonal Antibody Alternate Names CRISPR associated protein 9, SpyCas9 Isotype Mouse IgG1 κ Applications FC , IF , IHC , IP , WB |
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Antibody DetailsProduct DetailsReactive Species S. Pyogenes Host Species Mouse Immunogen Recombinant S. pyogenes Cas9 Protein (N-terminal 250 amino acids) expressed in E. coli. Product Concentration ≥1.0 mg/ml Purity ≥90% monomer by analytical SEC and SDS-Page Formulation 0.2 µm Filtered, Aseptically Packaged State of Matter Liquid Storage and Handling This antibody may be stored sterile as received at 2-8°C for up to one month. For longer term storage, aseptically aliquot in working volumes without diluting and store at -80°C. Avoid Repeated Freeze Thaw Cycles. Regulatory Status Research Use Only Country of Origin USA Shipping 2 – 8° C Wet Ice Additional Applications Reported In Literature ? IHC, IP, IF, WB, FC Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change. DescriptionDescriptionSpecificity 7A9-3A3 activity is directed against Cas9 and dCas9. Background The CRISPR/Cas9 system is an RNA-guided endonuclease system used for genome editing that was first identified as an adaptive immune system in bacteria and archaea1. To operate, a single guide RNA is responsible for DNA site targeting, while Cas9 cleaves the DNA at the target sites. Cas9 contains RuvC and HNH nuclease domains, which are responsible for cleaving the target complementary and noncomplementary DNA strands. Cas9 is directed to the specific DNA targets by the single guide RNA. Any DNA sequence that contains the N20-NGG motif can be recognized as a target site.
The CRISPR/Cas9 system has been engineered to allow genome editing in a variety of organisms beyond bacteria1. Codon-optimized Cas9 with an appropriate nuclear localization signal has been used in yeast, roundworm, silkworm, Drosophila, zebrafish, frog, rabbit, human, mouse, rat, pig, monkey, and plants. A single gene or multiple genes (e.g., at least four genes in rat, mouse, and zebrafish) can be disrupted by providing the appropriate single guide RNAs and programming the DNA-cleaving activity of Cas9. Large-fragment deletion, inversion, and reporter gene insertion can also be performed. Additionally, methylation effect and chromatin states can be studied using ‘dead’ Cas9, which is a fusion of a non-functional Cas9 with an effector domain. In mouse1, 2, 3 and humans, the CRISPR/Cas9 system has been used to correct genetic diseases (e.g., cystic fibrosis1, sickle cell disease4, and β-thalassemia) and also has applications for cancer treatment5. Antigen Distribution Cas9 is found naturally in the prokaryote Streptococcus pyogenes and can be introduced into various species for genome editing. NCBI Gene Bank ID UniProt.org Research Area Cell Biology . Neuroscience References & Citations1. Ma Y, Zhang L, Huang X. FEBS J. 281(23):5186-5193. 2014.
2. Savić N, Schwank G. Transl Res. 168:15-21. 2016. 3. Park H, Oh J, Shim G, et al. Nat Neurosci. 22(4):524-528. 2019. 4. Frangoul H, Altshuler D, Cappellini MD, et al. N Engl J Med. 384(3):252-260. 2021. 5. Wang SW, Gao C, Zheng YM, et al. Mol Cancer.21(1):57. 2022. 6. Lin S, Ewen-Campen B, Ni X, et al. Genetics. 201(2):433-442. 2015. 7. Howden SE, McColl B, Glaser A, et al. Stem Cell Reports. 7(3):508-517. 2016. 8. Kim S, Bae T, Hwang J, et al. Genome Biol. 18(1):218. 2017. 9. Lattanzi A, Duguez S, Moiani A, et al. Mol Ther Nucleic Acids. 7:11-19. 2017. 10. Maji B, Moore CL, Zetsche B, et al. Nat Chem Biol. 13(1):9-11. 2017. Technical ProtocolsCertificate of Analysis |
Formats Available
Products are for research use only. Not for use in diagnostic or therapeutic procedures.