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Concentration
10 - 30u/μl
5'…G↓GNCC…3' 
3'…CCNG↑G…5'

Reaction Conditions 
1X Buffer V4 
100mM Tris-HCl (pH 8.5 at 30°C), 10mM MgCl₂, 100mM KCl, and 100μg/ml BSA. Incubate at 37°C.

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

Thermal Inactivation
65°C for 20 minutes.

Ligation / Recutting Assay 
After 20-fold overdigestion with AspS9I, more than 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 20u of AspS9I for 16 hours at 37°C. 
Supplied with 10X Buffer V4, 10X Buffer UB and Viva Buffer A. (Diluent) 
*Blocked by overlapping dcm-methylation (C^mCWGG): GGNCCWGG

Ordering Information

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Manual
AspS9I {AsuI}