 | Source: Bacillus globigii lacking Bgl I.
Buffer supplied: 10x B3 (incl. 10x BSA).
Substrate for unit definition: λ DNA (6 sites).
Reaction conditions: 100 mM NaCl, 50 mM Tris-HCl (pH 7.9 @ 25°C), 10 mM MgCl2, 1 mM dithiothreitol, 100 µg/ml BSA. Incubate at 37°C. | | Storage buffer: 50 mM KCl, 10 mM Tris-HCl (pH 7.4), 0.1 mM EDTA, 1 mM dithiothreitol, 200 µg/ml BSA and 50 % glycerol. Store at -20°C.
Ligation and recutting: After 30-fold overdigestion with Bgl II, >95 % of the DNA fragments can be ligated and recut with this enzyme.
Heat inactivation: No. | |
