Concentration
3-30u/μl
5'…T↓CGA…3'
3'…AGC↑T…5'
Reaction Conditions
1X Buffer V5
30mM Tris-acetate (pH 7.9 at 30°C), 10mM Mg-acetate, 60mM K-acetate, and 100μg/ml BSA. Incubate at 65°C.
Storage Buffer
10mM Tris-HCl (pH 7.5), 200mM NaCl, 0.1mM EDTA, 7mM 2-mercaptoethanol, 200μg/ml BSA and 50% glycerol. Store at -20°C.
Thermal Inactivation
None.
Ligation / Recutting Assay
After 10-fold overdigestion with TaqI, 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 10u of TaqI for 16 hours at 65°C.
Supplied with 10X Buffer V5, 10X Buffer UB and Viva Buffer A. (Diluent)
*Blocked by overlapping dammethylation (GmATC): TCGATC.
Ordering Information
|
Catalog No
|
Description
|
Pack Size
|
|
RE1346
|
TaqI
|
2000u
|
Downloads
Manual
TaqI
