$ 66.30
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Conventional restriction endonucleases are a large collection of high quality restriction enzymes, optimized to work in one of the buffers of the Five Buffer System. In addition, the universal Tango buffer is provided for convenience in double digestions. All of the enzymes exhibit 100% activity in the recommended buffer and reaction conditions. To ensure consistent performance, Thermo Scientific restriction enzyme reaction buffers contain premixed BSA, which enhances the stability of many enzymes and binds contaminants that may be present in DNA preparations.5'...C C A N N N N N▵N T G G...3'3'...G G T N▵N N N N N A C C...5'Conditions for 100% Activity:b1X Buffer O: 50mM Tris-HCl (pH 7.5 at 37°C), 10mM MgCl2, 100mM NaCl and 0.1mg/mL BSAIncubate at 55°CStorage Buffer:BstXI is supplied in: 10mM Tris-HCl (pH 7.5 at 25°C), 50mM KCl, 1mM DTT, 0.1mM EDTA, 0.2mg/mL BSA and 50% (v/v) glycerolLigation and Recleavage:After 50-fold overdigestion with BstXI, approximately 95% of the DNA fragments can be ligated and recut Methylation Effects:Dam: never overlaps — no effectDcm: may overlap — cleavage impairedCpG: never overlaps — no effectEcoKI: never overlaps — no effectEcoBI: never overlaps — no effectDigestion of Agarose-embedded DNA:Minimum 5units of the enzyme are required for complete digestion of 1μg of agarose-embedded lambda DNA in 16hours Note:Incubation at 37°C results in 50% activity. Greater than 15-fold overdigestion with BstXI may result in star activity. BstXI cleavage is impaired by overlappingdcm methylation. To avoiddcm methylation, use adam-, dcm strain such as GM2163 (#M0099).