|5'|| || ||↓||N8||G ||A ||G ||N5||C ||T ||C ||N13||↓|| ||3'|
|3'|| || ||↑||N13||C ||T ||C ||N5||G ||A ||G ||N8||↑|| ||5'|
Thermo Scientific BplI restriction enzyme recognizes ^(8/13)GAG(N)5CTC(13/8)^ sites and cuts best at 37°C in Tango(+SAM) buffer. See Reaction Conditions for Restriction Enzymes
for a table of enzyme activity, conditions for double digestion, and heat inactivation for this and other restriction enzymes. Note: Also available as a FastDigest enzyme
for rapid DNA digestion.
Thermo Scientific 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.Features
• Superior quality—stringent quality control and industry leading manufacturing process
• Convenient color-coded Five Buffer System
• Includes universal Tango buffer for double-digestions
• BSA premixed in reaction buffers
• Wide selection of restriction endonuclease specificitiesApplications
• Molecular cloning
• Restriction site mapping
• Southern blotting
• Restriction fragment length polymorphism (RFLP)
BplI requires only Mg2+ for its activity, but is stimulated by S-adenosylmethionine. 0.05 mM S-adenosylmethionine gives more than a 100-fold increase in BplI activity. Still, complete cleavage of some substrates with BplI is difficult to achieve. BplI concentration is determined by the maximum cleavage level achieved when no change in the fragmentation pattern is observed with further enzyme increase. For methylation sensitivity, refer to product specifications.
For Research Use Only. Not for use in diagnostic procedures.