SibEnzyme restriction enzymes database

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Bbv12 I

Enzyme name Bbv12 I
Prototype HgiAI
SKU SE-E023
Turbo version Not available
High-concentration version Not available
Recognition site
5'… GWGCW▼C …3'
3'… C▲WCGWG …5'
Source Bacillus brevis 12
Optimal buffer SE-buffer O
Optimal temperature 37 °C
Inactivation temperature 80 °C
Buffer activity
BGOWYROSE
010100751060
Unit definition One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 37°C in a total reaction volume of 50 μl.
Assayed on Lambda DNA
Storage conditions 10 mM Tris-HCl (pH 7.5); 100 mM NaCl; 0.1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; 50% glycerol; Store at -20°C.
Ligation After 3-fold overdigestion with enzyme more than 90% of the DNA fragments can be ligated and recut.
Nonspecific hydrolysis No nonspecific activity was detected after incubation of 1 μg of Lambda DNA with 4 u.a. of enzyme for 16 hours at 37°C.
Methylation sensitivity not tested
Supplied with enzyme 10 X SE-buffer O
Notes
References
  1. Repin, V.E., Rechkunova, N.I., Degtyarev, S.Kh., Hachaturyan, A.A., Afrikyan, E.K. Biol. J. Armenia 42: 969-972 (1989).

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Bbv12 I

Enzyme name Bbv12 I
Prototype HgiAI
SKU SE-E023
Turbo version Not available
High-concentration version Not available
Recognition site
5'… GWGCW▼C …3'
3'… C▲WCGWG …5'
Source Bacillus brevis 12
Optimal buffer SE-buffer O
Optimal temperature 37 °C
Inactivation temperature 80 °C
Buffer activity
BGOWYROSE
010100751060
Unit definition One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 37°C in a total reaction volume of 50 μl.
Assayed on Lambda DNA
Storage conditions 10 mM Tris-HCl (pH 7.5); 100 mM NaCl; 0.1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; 50% glycerol; Store at -20°C.
Ligation After 3-fold overdigestion with enzyme more than 90% of the DNA fragments can be ligated and recut.
Nonspecific hydrolysis No nonspecific activity was detected after incubation of 1 μg of Lambda DNA with 4 u.a. of enzyme for 16 hours at 37°C.
Methylation sensitivity not tested
Supplied with enzyme 10 X SE-buffer O
Notes
References
  1. Repin, V.E., Rechkunova, N.I., Degtyarev, S.Kh., Hachaturyan, A.A., Afrikyan, E.K. Biol. J. Armenia 42: 969-972 (1989).