Benzonase Endonuclease
Benzonase endonuclease from Serratia marcescens, can be used to degrade all forms of DNA and RNA while having no proteolytic activity.
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Description:
Exonuclease III (E. coli) is a 3' -> 5' exonuclease which acts by digesting one strand of a dsDNA duplex at a time or digesting the RNA strand of an RNA-DNA heteroduplex(1,2). Exonuclease III (E. coli) breaks phosphodiester bonds on the 5'-side of AP sites in both dsDNA and ssDNA(3). It removes 3'-terminal groups on dsDNA(3), increases MutY turnover(4), and efficiently degrades 3'-recessed but not 3' protruding DNA ends (creating 5'-overhangs)(5). Exonuclease III (E. coli) removes a limited number of nucleotides per binding event, resulting in coordinated progressive deletions within the population of DNA molecules(1).
Specific Activity: 150,000 U/mg
Application:
Degrades excess single-stranded primer oligonucleotides from a reaction mixture containing double-stranded extension products.
Source:
Purified from a strain of E. coli that expresses the recombinant Exonuclease III gene.
Supplied in:
25 mM Tris-HCl
50 mM KCl
1.0 mM DTT
0.1% mM EDTA
50% Glycerol
pH 8.0 @ 25°C
Supplied with: 10x Yellow Buffer
10x Yellow Buffer:
100 mM Bis-Tris-Propane
100 mM MgCl2
10 mM DTT
pH 7.0 @ 25°C
Unit Definition:
One unit is defined as the amount of enzyme required to produce 1 nmol of acid-soluble total nucleotide in 30 minutes at 37°C.
Recommended Storage Condition: -20°C
References:
1. Linn, S. M. (1982) Nucleases, pp. 291-309, Cold Spring Harbor Laboratory Press.
2. Shida, T., et al. (1996) Nucl. Acids Res. 24 (22), 4572-4576.
3. Doetsch, P. W. (1990) Mutat. Res. 236 (2-3), 173-201.
4. Pope, M. A., et al. (2002) J. Biol. Chem. 277 (25), 22605-22615.
5. Henikoff, S. (1984) Gene 28, 351-359.
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Benzonase endonuclease from Serratia marcescens, can be used to degrade all forms of DNA and RNA while having no proteolytic activity.
CRISPR-Cas systems are powerful tools for mediating nucleic acids. Cas12a (also referred as Cpf1) nuclease belonging to the Class 2, Type V CRISPR system.
LbCas12a (D832A, with an Asp832→Ala substitution)
Origin: Lachnospiraceae bacterium (strain ND2006)
Purity > 95%
Adaptive immune systems from prokaryotes utilize clustered regularly interspaced short palindromic repeats (CRISPRs) and CRISPR associated (Cas) proteins to cleave foreign genetic material. CasRx, Cas13d from Ruminococcus flavefaciens XPD3002, is highly active and short, 94KD.
Fast and simple fragmentation
Fragment size easily controlled by incubation time
Ideal for NGS library preparation
Adaptive immune systems from prokaryotes utilize clustered regularly interspaced short palindromic repeats (CRISPRs) and CRISPR associated (Cas) proteins to cleave foreign genetic material. Cas13a, (previously referred to as C2c2) is part of the Type VI CRISPR-Cas system.
Fast and simple fragmentation
Fragment size easily controlled by incubation time
Ideal for NGS library preparation
Adaptive immune systems from prokaryotes utilize clustered regularly interspaced short palindromic repeats (CRISPRs) and CRISPR associated (Cas) proteins to cleave foreign genetic material. CasRx, Cas13d from Ruminococcus flavefaciens XPD3002, is highly active and short, 94KD.
25,000 units, 100,000 U/ml
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