GenCRISPR™ LbCas12a Nuclease
| $189.00 | |
| Z03753-100 | |
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| Ask us a question | |
IVD Raw Materials
| $189.00 | |
| Z03753-100 | |
|
|
|
|
|
|
|
|
|
| Ask us a question | |
| Description | GenCRISPR™ LbCas12a Nuclease is an RNA-guided DNA endonuclease from Lachnospiraceae bacterium. Cas12a (previously known as Cpf1) belongs to the Class 2 Type V CRISPR/Cas system. Different from CRISPR/Cas9 system, the ribonucleoprotein (RNP) complex of CRISPR/Cas12a system is formed by Cas12a and crRNA, it recognizes a T-rich protospacer adjacent motif (PAM) and results in a staggered DNA double-strand break (DSB). After the specific cleavage, Cas12a can also activate collateral cleavage activity towards adjacent non-specific ssDNA sequences. Hence, Cas12a nuclease is a good alternative for Cas9 in certain target DNA editing, and provides a novel strategy for DNA detection. |
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crRNA-dependent DNA cleavage |
| Source |
Recombinant Cas12a with a C-terminal NLS
expressed by E.coli |
| Species |
Lachnospiraceae bacterium |
| PAM | TTTV |
| Tag |
C-terminal 6× His Tag |
| Apparent Molecular Weight |
146 kDa, on SDS-PAGE under non-reducing
conditions |
| Concentration |
4 mg/ml |
| Storage Buffer |
10 mM Tris-HCl, 300 mM NaCl, 0.5 mM DTT, 50%
glycerol, pH 7.4. |
| Storage & Stability |
Store
at -20 °C for 12 months from the date of manufacture. Avoid repeated
freeze-thaw cycles. Do not store below
-20 °C! |
| Accession# |
6KL9_A |
| Appearance |
Clear, colorless liquid |
| Purity |
≥ 90% by SDS-PAGE |
| Concentration |
4(± 10%) mg/ml |
| Bioactivity |
≥ 90% |
| Residual DNase |
Undetectable |
| Residual RNase |
Undetectable |
| Endotoxin Level |
< 0.1 EU/μg |
Figure 1: In vitro digestion efficiency analysis by agarose gel electrophoresis. A 20 μl reaction in 1 × Cas12a Nuclease Reaction Buffer containing 60 ng linearized plasmid, 10 ng crRNA, and 100 ng GenCRISPR™ LbCas12a Nuclease (Cat. No. Z03753) for 30 min at 37°C results in a digestion efficiency of linearized plasmid higher than 90%, as determined by agarose gel electrophoresis. »
| References |
Chen, Janice S., et al.
"CRISPR-Cas12a target binding unleashes indiscriminate single-stranded
DNase activity." Science
360.6387 (2018): 436-439. 2. Ledford, Heidi. "Alternative CRISPR system could improve genome editing." Nature News 526.7571 (2015): 17. 3. Chen, Janice S., et al. "CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity." Science 360.6387 (2018): 436-439. |
For laboratory research use only. Direct human use,
including taking orally and injection and clinical use are forbidden.