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- 文献和实验
- 技术资料
- 库存:
大量
- 英文名:
Bsh1236I (BstUI) (10 U/µL)
- 保质期:
1年
- 供应商:
上海沪震实在有限公司
- 保存条件:
-20℃
- 规格:
500units
Bsh1236I (BstUI) (10 U/µL)
Enzyme : Bsh1236I (BstUI)保存温度 : -20℃
货期 : 2-3天
Compatible Buffer : 10x Buffer R
Optimal Reaction Temperature : 37° C
Sensitive to Heat Inactivation: : Yes
Methylation Sensitivity : CpG methylation-sensitive, Not dam methylation-sensitive, Not dcm methylation-sensitive
5' C G ↓ C G 3'
3' G C ↑ G C 5'
Thermo Scientific Bsh1236I (BstUI) restriction enzyme recognizes CG^CG sites and cuts best at 37°C in R buffer (isoschizomers: AccII, BspFNI, BstFNI, BstUI, MvnI). 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 specificities
Applications
• Molecular cloning
• Restriction site mapping
• Genotyping
• Southern blotting
• Restriction fragment length polymorphism (RFLP)
• SNP
Note: For methylation sensitivity, refer to product specifications.
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文献和实验Cleavage Efficiency Close to the&nbs
in the DNA Extraction Kit (#K0513) followed by ethanol precipitation. DNA (0.5µg) and 10u of restriction endonuclease were incubated for 1 hour at the recommended incubation temperature and optimal buffer for each enzyme in a total volume of 40µl. Reaction
Cleavage Efficiency Close to the Termini of PCR Fragments
in the DNA Extraction Kit (#K0513) followed by ethanol precipitation. DNA (0.5µg) and 10u of restriction endonuclease were incubated for 1 hour at the recommended incubation temperature and optimal buffer for each enzyme in a total volume of 40µl. Reaction
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