PalA I

Restriction endonuclease PalA I

  • Recognition site: GG↑CGCGCC / CCGCGC↓GG
  • Источник: Из штамма E. coli, несущего клонированный ген PalA I из Pseudomanas alcaligenes BS17
  • Оптимальный буфер: SE-буфер Y
  • Оптимальная температура: 37
  • Температура инактивации, 20 мин при: 65
SKU: SE-E483 Category:

Description

Recognition site and hydrolysis position:

GGCGCGCC GG↑CGCGCC
CCGCGCGG CCGCGC↓GG

Source: An E. coli strain , that carries the cloned gene from Pseudomanas alcaligenes BS17Unit 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 Y
Enzyme activity (%):

B G O W Y ROSE
25 10 -10 -10 100 40

Storage conditions: 10 mM Tris-HCl (pH 7.5); 100 mM KCl; 0.1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; 50% glycerol; Store at -20°C.
Ligations:
After 5-fold overdigestion with enzyme more than 90% of the DNA fragments can be ligated and 95% of these can be recut.
Non-specific hydrolisis:
No nonspecific activity was detected after incubation of 1 μg of Lambda DNA with 5 u.a. of enzyme for 16 hours at 37°C.Reagents Supplied with Enzyme

10 X SE-buffer Y
Reagents Supplied with Enzyme:
Methylation sensitivity: Blocked by CG methylation.
Notes:
References:
Dedkov, V.S., Belichenko, O.A., Gonchar, D.A., Akishev, A.G., Yamkovaya, T.V., Mezentseva, N.V., Tomilova, J.E., Abdurashitov, M.A., Degtyarev, S.K. Unpublished observations(2005)