EcoR V

2,090.00 8,360.00 

  • CNY: 162.54 ¥ - 650.16 ¥

Restriction endonuclease EcoR V

  • Recognition site: GAT↑ATC / CTA↓TAG
  • Источник: Из штамма Е.coli несущего клонированный ген EcoRV из Escherichia coli
  • Оптимальный буфер: SE-буфер W
  • Оптимальная температура: 37
  • Температура инактивации, 20 мин при: 80
SKU: SE-E059 Category:

Available Options

SKUРackagePackageVariantConcentrationPrice 
E059S2000 uRegular20 000 u/ml2,090.00 
  • CNY: 162.54 ¥
E060L10000 uRegular20 000 u/ml8,360.00 
  • CNY: 650.16 ¥
E059TS2000 uTurbo20 000 u/ml2,090.00 
  • CNY: 162.54 ¥
E060TL10000 uTurbo20 000 u/ml8,360.00 
  • CNY: 650.16 ¥

Description

Recognition site and hydrolysis position:

GATATC GAT↑ATC
CTATAG CTA↓TAG

Source: An E.coli strain, that carries the cloned gene EcoRV from Escherichia coli
Unit definition:
One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 37°C in a total reaction volume of 50 μl.
Assayed on:
Lambda DNA
Optimal SE-buffer: SE-buffer W
Enzyme activity (%):

B G O W Y ROSE
0 25 50 100 25 50

Storage conditions: 10 mM Tris-HCl (pH 7.5); 50 mM NaCl; 0,1 mM EDTA; 1 mM DTT; 200 μg/ml BSA; 50% glycerol; Store at -20°C.
Ligations:
After 20-fold overdigestion with enzyme 90% of the DNA fragments can be ligated and recut.
Non-specific hydrolisis:
No nonspecific activity was detected after incubation of 1 μg of Lambda DNA with 20 u.a. of enzyme fro 16 hours at 37°C. Reagents Supplied with Enzyme 10 X SE-buffer W, BSA
Reagents Supplied with Enzyme:
Methylation sensitivity: not tested
Notes: High enzyme concentration results in star activity.
Do not use BSA for long incubation
To obtain 100% activity, BSA should be added to the 1 x reaction mix to a final concentration of 100 μg/ml.
References:
Kholmina, .V., Rebentish, B.A., Skoblov, Yu.S., et.al. Dokl.Akad. Nauk SSSR 253: 495-497 (1980).
Chernukhin V.A, Abdurashitov M.A., Tomilov V.N., Gonchar D.A., Degtyarev S.Kh. Comparative analysis of mouse chromosomal DNA digestion with restriction endonucleases in vitro and in silico // Translated from “Ovchinnikov bulletin of biotechnology and physical and chemical biology” V.3, No 4, pp 19-27, 2007