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Concentration
10-50u/μl
5'…C↓TNAG…3' 
3'…GANT↑C…5'

Reaction Conditions 
1X Buffer V2 
10mM Tris-HCl (pH 7.5 at 30°C), 10mM MgCl₂, 50mM NaCl, and 100μg/ml BSA. Incubate at 60°C.

Storage Buffer
10mM KH₂PO₄ (pH 7.5), 50mM KCl, 0.1mM EDTA, 7mM 2-mercaptoethanol, 200μg/ml BSA and 50% glycerol. Store at -20°C.

Thermal Inactivation
None.

Ligation / Recutting Assay 
After 20-fold overdigestion with BstDEI, 90% of the DNA fragments can be ligated and recut.

Overdigestion Assay 
An unaltered banding pattern was observed after 1μg of DNA was digested with 40u of BstDEI for 16 hours at 60°C.
Supplied with 10X Buffer V2, 10X Buffer UB and Viva Buffer A. (Diluent)

Ordering Information

Downloads
Manual
BstDEI {DdeI}