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- 详细信息
- 文献和实验
- 技术资料
- 库存:
大量
- 英文名:
MunI (MfeI) (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
MunI (MfeI) (10 U/µL)
Enzyme : MunI (MfeI)保存温度 : -20℃
货期 : 2-3天
Compatible Buffer : 10x Buffer G
Optimal Reaction Temperature : 37° C
Sensitive to Heat Inactivation: : Yes
Methylation Sensitivity : Not CpG methylation-sensitive, Not dam methylation-sensitive, Not dcm methylation-sensitive
5' C ↓ A A T T G 3'
3' G T T A A ↑ C 5'
Thermo Scientific MunI (MfeI) restriction enzyme recognizes C^AATTG sites and cuts best at 37°C in G buffer (Isoschizomers: MfeI). 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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文献和实验请问有哪些原核表达载体的mcs含有以下三个以上以下的酶切位点。谢谢 AarI CACCTGC,4,8 MfeI C/AATTG AatII GACGT/C MluI A/CGCGT AccI GT/MKAC MmeI TCCRAC,20,18 AceII GCTAG/C MscI TGG/CCA AclI AA/CGTT NaeI GCC/GGC AfeI AGC/GCT NarI GG/CGCC AflII C/TTAAG NdeI CA/TATG AgeI
Generating stable cell lines in HEK293
diameter according to the protocol for transient transfection in HEK. About 16 hrs post transfection, exchange the medium to medium supplemented with 0.5 g/L of neomycin. Keep exchanging the medium every day for 7-10 days. This is the time needed
内Hirt’S小分子DNA抽提及分析 按照Hirt’S方法 在转染后14、28、60 d抽提COS.7细胞内小分子DNA。具体方法:用10 mmol/L Tris.HC1(pH 7.5,1 mmoI/L EDTA,1% SDS,200 g/mL Pro—teinase K)1 mL裂解5×10。个细胞,37℃ 保温2 h;裂解细胞液内加入5 mol/L NaC1 0.25 mL,轻轻混匀,4℃ 过夜;4℃ 离心,15 000×g 30 min;取上清,酚一氯仿抽提,乙醇沉淀,20 TE液(pH 8.
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