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Potvrzuji
  1. Úvodní strana
  2. Reagencie
  3. DNA/RNA modifikující enzymy
  4. Deoxyribonucleases (DNases)
  5. Endonuclease V, T.maritima

Endonuclease V, T.maritima

Kód produktu: EN0141 Kód výrobce: EN0141 Kód dodavatele: {5E003C8E-AA76-43FD-8767-00091273E42F} Výrobce: Life Technologies Czech Republic s.r.o.
Endonuclease V, T.maritima
3 236,75 Kč
2 675,00 Kč bez DPH
do týdne
250 Units
Endonuclease V, T. maritima (Endo V) is a  3'-endonuclease involved in DNA repair, which initiates removal of deaminated bases from damaged DNA, including uracil, hypoxanthine, and xanthine.
Zobraz detailní popis
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Detailní popis

Thermo Scientific Endonuclease V, T. maritima (Endo V) is a  3'-endonuclease involved in DNA repair, which initiates removal of deaminated bases from damaged DNA, including uracil, hypoxanthine, and xanthine (see Figure 1).

Endonuclease V is also active toward abasic sites and urea sites, base pair mismatches, flap and pseudo Y structures, and small insertions/deletions in DNA molecules. The cleavage site generated by Endonuclease V is at the second phosphodiester bond 3' to a lesion. 

Highlights

  • Optimal activity at temperatures of 65 to 70°C

Applications

  • High-throughput methods for mutation research (see​ References 3,4)
  • Studies in mutagenesis and DNA repair
  • Mismatch cleavage
  • Genotyping

Note

Use of this enzyme in certain applications may be covered by patents and may require a license. 

When the enzyme is in excess, the primary nicked products experience a  second nicking event on the complementary strand, leading to a  double-stranded break. At low concentrations, however, Endonuclease V  first nicks a DNA strand at the lesions located closer to the 5'-end of DNA molecule. Single-stranded DNA is cleaved with much lower efficiency. Mg2+ or Mn2+ ions are required for enzyme activity (see References 1-3).

10X Reaction Buffer 500 mM Tris-acetate (pH 7.5), 500 mM KCl, 10 mM EDTA, 0.5% (v/v) Triton X-100.
CategoryName
Concentration 5 U/µL
Definition of Activity Unit
  • One unit of the enzyme converts 1 µg of supercoiled depurinized plasmid DNA into other topological states in 30 min at 65°C.
  • Enzyme activity is assayed in the following mixture: 25 mM HEPES-NaOH (pH 7.4), 5 mM MgCl2, 5 mM DTT, 2% (v/v) glycerol, 2 µg of partially depurinated pUC19 DNA.
Hazardous No
Hazardous: No
Inactivation Inactivated by heating in boiling water bath for 10 min, preferably in the presence of EDTA.
Inhibition Inhibitors: no specific inhibitors have been described.
Molecular Weight 25 kDa monomer.
Quality Control The absence of other endo-, exodeoxyribonucleases, and ribonucleases confirmed by appropriate quality tests.
Shelf Life:
Shipping Condition:
Shipping Information
Source E.coli with a cloned nfi gene of Thermotoga maritima 
SpecificationName
SpecificationValue
Storage Buffer The enzyme is supplied in:
20 mM HEPES-NaOH (pH 7.4), 5 mM DTT, 50 mM NaCl, 0.1% (v/v) Triton X-100 and 50% (v/v) glycerol.
Storage Condition -20 C
Storage Condition: -20 C

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