产地:MBI
货号:ER1641
Conditions for 100% Activity
1X Buffer G:
10 mM Tris-HCl (pH 7.5 at 37°C), 10 mM MgCl2, 50 mM NaCl and 0.1 mg/ml BSA.
Incubate at 37°C.
Ligation and Recleavage
After 50-fold overdigestion with SatI, more than 60% of the DNA fragments can be ligated in a reaction mixture containing 10-30 u of T4 DNA Ligase/1 µg of fragments and 10% PEG. More than 90% of these can be recut.
Storage Buffer
SatI is supplied in:
10 mM Tris-HCl (pH 7.4 at 25°C), 100 mM KCl, 1 mM DTT, 1 mM EDTA, 0.2 mg/ml BSA and 50% (v/v) glycerol.
ER1641 | 200 u (10 u/µl) | 1.00 ml | 1.00 ml | ER1641 | |
ER1642 | 1000 u (10 u/µl) | 1.00 ml | 1.00 ml | ER1642 | |