Recognition Sequence :
GG↑CGCC
CCGC↓GG
Unit Definition :
One unit of the enzyme is the amount required to hydrolyze 1 μg of T7 DNA 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 KCl; 0.1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; 50% glycerol
Ligation :
After 3-fold overdigestion with enzyme more than 80% of the DNA fragments can be ligated and recut.
Source :
Micrococcus lylae 113
Working buffer :
B (10 mM Tris-HCl (pH 7.6 at 25°C); 10 mM MgCl2; 1 mM DTT.)
Non-specific hydrolisis :
No nonspecific activity was detected after incubation of 1 μg of T7 DNA with 2 u.a. of enzyme for 16 hours at 37°C.
Concentration, u.a./ml :
2000
Inactivation :
20min Under 65°C
Reagents Supplied :
10 X SE-buffer B
Notes :
High enzyme concentration may result in star activity.
Our Products Cannot Be Used As Medicines Directly For Personal Use.
PDF