Bst2U I

Enzyme nameBst2U I
PrototypeBstNI
Known analogsBptI, BseBI, BstNI, BstOI, MvaI, Ajn I, EcoRII, Psp6 I, PspGI
SKUSE-E051
Turbo versionNot available
High-concentration versionNot available
Restriction typeType IIPiType IIP enzymes are classical Type II restriction enzymes with palindromic recognition sequences and symmetric cleavage sites.
Recognition site
5'… CC▼WGG …3'
3'… GGW▲CC …5'
SourceBacillus stearothermophilus 2U
Optimal bufferSE-buffer G (10 mM Tris-HCl (pH 7.6 at 25°C); 10 mM MgCl2; 50 mM NaCl; 1 mM DTT.)
Optimal temperature60 °C
Inactivation temperatureне инактивируется
Buffer activity
BGOWYROSE
7510050501050
Unit definitionOne unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 60°C in a total reaction volume of 50 μl.
Assayed onLambda DNA
Storage conditions10 mM Tris-HCl (pH 7.5); 200 mM NaCl; 0.1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; 50% glycerol. Store at -20°C.
Ligation
Nonspecific hydrolysisNo nonspecific activity was detected after incubation of 1 μg of Lambda DNA with 20 u.a. of enzyme for 16 hours at 60°C.
Methylation sensitivityNot blocked by overlapping Dcm methylation(C m CWGG) CCWGG.
Reagents supplied with enzyme10 X SE-buffer G, BSA
NotesTo obtain 100% activity, BSA should be added to the 1x reaction mix to a final concentration of 100 μg/ml. Do not use BSA for long incubation.
References
  1. Unpublished data Myakisheva, T.V., Degtyarev, S.K Unpublished observations (1995).
// Код для некролога