Recognition Sequence :
GAAGA(N)8↑
CTTCT(N)7↓
Unit Definition :
One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA (dam-) in 1 hour at 37°C in a total reaction volume of 50 μl.
Reaction Temperature :
37°C
Storage Buffer :
10 mM Tris-HCl (pH 7.5); 50 mM NaCl; 0,1 mM EDTA; 1 mM DTT; 200 μg/ml BSA; 50% glycerol.
Ligation :
After 5-fold overdigestion with enzyme approximately 60% of the DNA fragments can be ligated and recut. In presence of 10%PEG ligation is better.
Source :
An E.coli strain, that carries the cloned gene Mbo II from Moraxella bovis
Assayed on :
Lambda DNA (dam-)
Working buffer :
Y (33 mM Tris-acetate (pH 7.9 at 25°C); 10 mM magnesium acetate; 66 mM potassium acetate; 1 mM DTT.)
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.
Concentration, u.a./ml :
5000
Inactivation :
20min Under 65°C
Methylation sensitivity :
Blocked by overlappin dam-methylation(GmATC): GAAGATC.
Reagents Supplied :
10 X SE-buffer Y
Our Products Cannot Be Used As Medicines Directly For Personal Use.
PDF