Vivantis Technologies Sdn Bhd

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

Download
Manual
BstDEI {DdeI}

Download
MSDS
BstDEI {DdeI}