SibEnzyme restriction enzymes database

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Acs I

Enzyme name Acs I
Prototype ApoI
SKU SE-E013
Turbo version Available
High-concentration version Not available
Recognition site
5'… R▼AATTY …3'
3'… YTTAA▲R …5'
Source Arthrobacter citreus
Optimal buffer SE-buffer W + BSA
Optimal temperature 50 °C
Inactivation temperature 80 °C
Buffer activity
BGOWYROSE
25505010010100
Unit definition One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 50°C in a total reaction volume of 50 μl.
Assayed on Lambda DNA
Storage conditions 20 mM Tris-HCl (pH 7.5); 50 mM KCl; 0.1 mM EDTA; 10 mM 2-mercaptoethanol; 50% glycerol; Store at -20°C.
Ligation After 10-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 20 u.a. of enzyme for 16 hours at 50°C.
Methylation sensitivity not tested
Supplied with enzyme 10 X SE-buffer W, BSA
Notes To 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. Degtyarev, S.Kh., Kolyhalov, A.A., Rechkunova, N.I., Abdurashitov, M.A., Nucleic Acids Res. 20: 3789 (1992). Chernukhin V.A, Abdurashitov M.A., Tomilov V.N., Gonchar D.A., Degtyarev S.Kh. Comparative analysis of mouse chromosomal DNA digestion with restriction endonucleases in vitro and in silico // Translated from "Ovchinnikov bulletin of biotechnology and physical and chemical biology" V.3, No 4, pp 19-27, 2007

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Acs I

Enzyme name Acs I
Prototype ApoI
SKU SE-E013
Turbo version Available
High-concentration version Not available
Recognition site
5'… R▼AATTY …3'
3'… YTTAA▲R …5'
Source Arthrobacter citreus
Optimal buffer SE-buffer W + BSA
Optimal temperature 50 °C
Inactivation temperature 80 °C
Buffer activity
BGOWYROSE
25505010010100
Unit definition One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 50°C in a total reaction volume of 50 μl.
Assayed on Lambda DNA
Storage conditions 20 mM Tris-HCl (pH 7.5); 50 mM KCl; 0.1 mM EDTA; 10 mM 2-mercaptoethanol; 50% glycerol; Store at -20°C.
Ligation After 10-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 20 u.a. of enzyme for 16 hours at 50°C.
Methylation sensitivity not tested
Supplied with enzyme 10 X SE-buffer W, BSA
Notes To 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. Degtyarev, S.Kh., Kolyhalov, A.A., Rechkunova, N.I., Abdurashitov, M.A., Nucleic Acids Res. 20: 3789 (1992). Chernukhin V.A, Abdurashitov M.A., Tomilov V.N., Gonchar D.A., Degtyarev S.Kh. Comparative analysis of mouse chromosomal DNA digestion with restriction endonucleases in vitro and in silico // Translated from "Ovchinnikov bulletin of biotechnology and physical and chemical biology" V.3, No 4, pp 19-27, 2007