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- 详细信息
- 文献和实验
- 技术资料
- 库存:
大量
- 英文名:
Cfr9I (XmaI) (10 U/µL)
- 保质期:
1年
- 供应商:
上海沪震实业有限公司
- 保存条件:
2-8℃保存
- 规格:
300units
Cfr9I (XmaI) (10 U/µL)
Enzyme : Cfr9I (XmaI)保存温度 : -20℃
货期 : 2-3天
Compatible Buffer : Unique Buffer (10x Buffer Cfr9I (XmaI))
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 ↓ C C G G G 3'
3' G G G C C ↑ C 5'
Thermo Scientific Cfr9I (XmaI) restriction enzyme recognizes C^CCGGG sites and cuts best at 37°C in its own unique buffer (Isoschizomers: TspMI, XmaCI). 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: To achieve complete digestion of substrate with Cfr9I, the concentration of DNA should be no less than 50 µg/mL in the reaction buffer.
For methylation sensitivity, refer to product specifications.
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文献和实验Methylation analyis using restriction enzyme digestion
DNA of quality sufficient for restriction digestion. Digest 10 µg of DNA overnight with a first enzyme, cutting out the fragment of interest in combination with HpaII, and another 10 µg with first enzyme in combination with MspI. Reaction
Methylated CpG Island Amplification
Methylated CpG Island Amplification Protocol written by Minoru Toyota 2.Materials 2.1.MCA Restriction enzymes SmaI,XmaI T4 DNA ligase Taq DNA polymerase 10X PCR reaction buffer: 670mM Tris-HCl,pH 8.8 40mM MgCl2 160 mM NH4 (SO4
Methylated CpG Island Amplification
Prepare tubes containing 10 m l of 10 X PCR buffer, 100 pmol of RXMA24 (or RMCA24) primers, 15 Units of Taq DNA polymerase, 1.2 m l dNTP mix (25mM), 0 m l (RXMA) or 5 m l (RMCA) DMSO, H2 O to a total volume of 97 m l. Add 3 m l of ligation mixture
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