I-SceI (10 U/µL)

I-SceI (10 U/µL)

Enzyme : I-SceI
保存温度 : -20℃
货期 : 2-3天
Compatible Buffer : 10x Buffer Tango
Optimal Reaction Temperature : 37° C
ensitive to Heat Inactivation: : Yes
Methylation Sensitivity : Not CpG methylation-sensitive, Not dam methylation-sensitive, Not dcm methylation-sensitive
5'              T      A      G      G      G      A      T      A      A ↓    C      A      G      G      G      T      A      A      T           3'     
3'              A      T      C      C      C ↑    T      A      T      T      G      T      C      C      C      A      T      T      A           5'     

Thermo Scientific I-SceI homing enzyme recognizes TAGGGATAA^CAGGGTAAT sites and cuts best at 37°C in Tango 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.

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 specificities

Applications

• Molecular cloning
• Restriction site mapping
• Genotyping
• Southern blotting
• Restriction fragment length polymorphism (RFLP)
• SNP

Note: Homing enzymes do not have stringently defined recognition sequences. They can tolerate minor sequence changes, which only partially affect the cleavage reaction. I-SceI may remain associated with the cleaved DNA. This may cause DNA band shifting during electrophoresis. To avoid atypical DNA band patterns, use the 6X DNA Loading Dye & SDS Solution for sample preparation or heat the digested DNA in the presence of SDS prior to electrophoresis. Assayed using pUC-I-SceI DNA.