CRISPR-Cas13a Antibody Summary
Ser2-Asn1300
Accession # WP_003034647
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of CRISPR-Cas13a by Western Blot. Western blot shows recombinant Francisella tularensis protein. PVDF membrane was probed with 1 µg/mL of Rabbit Anti-CRISPR-Cas13a Monoclonal Antibody (Catalog # MAB10463) followed by HRP-conjugated Anti-Rabbit IgG Secondary Antibody (HAF008). A specific band was detected for CRISPR-Cas13a at approximately 143 kDa (as indicated). This experiment was conducted under reducing conditions and using Western Blot Buffer Group 1.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: CRISPR-Cas13a
Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-associated endonuclease from Prevotella and Francisella 1, Cpf1, also known as Cas12a, is a 1200-1500 amino-acids long monomeric protein that belongs to the CRISPR/Cas system (1, 2), an adaptive immune system of prokaryotes that has now become a powerful tool for genome editing (3). CRISPR/Cpf1 belongs the class II (type 5) of the CRISPR/Cas system that is defined by a single-subunit effector (4). Cpf1 has recently emerged as an alternative for Cas9, due to its distinct features (2, 5) such as the ability to target T-rich motifs, no need for trans-activating crRNA, inducing a staggered double-strand break and potential for both RNA processing and DNA nuclease activity. In addition, Cpf1 is able to process more structured pre-CRISPR/RNA(crRNA) molecules into mature crRNAs (6) which allows the possibility to use both mature or pre-crRNA for genome editing purposes(7). All these features make the CRISPR-Cpf1 system a valuable genome-engineering tool (8). CRISPR-Cpf1(Cas12a) has been successfully used to edit genomes in mammalians cells (2), plants (9), mice (10), Drosophila (11) and recently zebrafish and Xenopus (7). Two Cpf1 orthologs have been commonly used for genome editing in different organisms: AsCpf1 and LbCpf1, which are derived from Acidaminococcus sp. BV3L6 and Lachnospiraceae bacterium ND2006, respectively (8).The attached nuclear localization signals (NLSs) on the chimeric protein ensures nuclear compartmentalization in cells during gene editing (12).
- Jinek, M. et al. (2012) Science 337:816.
- Zetsche, B. et al. (2015) Cell 163:759.
- Sandler J.D. and Joung J.K. (2014) Nat Biotechnol. 32:347.
- Koonin E.V. et al. (2017) Curr. Opin. Micrbiol. 37:67.
- Bayat H. et al. (2018) Curr. Micribiol. 75:107.
- Fonfara, I. et al. (2016) Nature 532:517.
- Moreno-Mateo, M.A. et al. (2017) Nat. Commun 8:2024.
- Joung K.J. et al. (2016) Nat. Biotechnol. 34:869.
- Kim, H et al. (2017) Nat. Commun. 8:14406.
- Kim, Y. et al. (2016) Nat. Biotechnol. 34:808.
- Port, F. and Bullock, S.L. (2016) Nat Methods 13:852.
- Cong, L. et al. (2013) Science 339:819.
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