Concentration1-10u/μl5"…TGC↓GCA…3" 3"…ACG↑CGT…5"
Reaction Conditions 1X Buffer UB 25mM Tris-acetate (pH 7.6 at 30°C), 10mM Mg-acetate, 100mM K-acetate, 7mM 2-mercaptoethanol, and 50μg /ml BSA. Incubate at 37°C.
Storage Buffer10mM Tris-HCl (pH 7.5), 200mM KCl, 0.1mM EDTA, 7mM 2-mercaptoethanol, 200μg/ml BSA, and 50% glycerol. Store at -20°C.
Thermal Inactivation65°C for 20 minutes.
Ligation / Recutting Assay After 10-fold overdigestion with Acc16l, more than 80% 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 Acc16I for 16 hours at 37°CSupplied with 10X Buffer UB and Viva Buffer A. (Diluent)
Ordering Information
Catalog No | Description | Pack Size |
RE1102 | Acc16I {MstI} | 200u |
DownloadsManualAcc16I {MstI}
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