Source: Curtobacterium citreus
Assayed on: Lambda DNA
Unit definition: One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 55°C in a total reaction volume of 50 μl.
Optimal SE-buffer: W (10 mM Tris-HCl (pH 8.5 at 25°C); 10 mM MgCl2; 100 mM NaCl; 1 mM DTT.) + BSA
Activity in SEBuffers:
SEBuffer B 0 - 10%
SEBuffer G 10 - 25%
SEBuffer O 25 - 50%
SEBuffer W 100%
SEBuffer Y 75 -100%
SEBuffer ROSE 100%
When using a buffer other than the optimal (suppied) SEBuffer, it may be necessary to add more enzyme to achieve complete digestion.
Optimal temperature: 55°C
Storage conditions: 10 mM Tris-HCl (pH 7.5); 100 mM NaCl; 0,1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; 50% glycerol.
Store: at -20°C.
Ligation: After 20-fold overdigestion with enzyme about 90% of the DNA fragments can be ligated and recut.
Non-specific hydrolisis: No nonspecific activity was detected after incubation of 1 μg of DNA with 40 u.a. of enzyme for 16 hours at 55°C.
Reagents supplied with Enzyme: 10 X SE-buffer W, BSA
Methylation sensitivity: not tested
Inactivation: 20 minutes under 80°C
Notes: 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.
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