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Concentration
10-20u/μl
5'…T↓TAA…3'
3'…AAT↑T…5'

Reaction Conditions 
1X Buffer V1
10mM Tris-HCl (pH 7.5 at 30°C), 10mM MgCl₂, and 100μg/ml BSA. Incubate at 65°C.

Storage Buffer
10mM Tris-HCl (pH 7.5), 50mM KCl, 0.1mM EDTA, 1mM DTT, 200μg/ml BSA and 50% glycerol. Store at -20°C.

Thermal Inactivation
None.

Ligation / Recutting Assay 
After 10-fold overdigestion with Tru9 I, more than 95% 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 Tru9I for 16 hours at 65°C.
Supplied with 10X Buffer V1, 10X Buffer UB and Viva Buffer A. (Diluent)
*Blocked by TTA^mA methylation

Ordering Information

Downloads
Manual
Tru9I