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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
Eco88I (AvaI) (10 U/µL)
- 规格:
1,000 units
描述
| 5' | C ↓ | Y | C | G | R | G | 3' | ||||
| 3' | G | R | G | C | Y ↑ | C | 5' |
Thermo Scientific Eco88I (AvaI) restriction enzyme recognizes C^YCGRG sites and cuts best at 37°C in 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. Note: Also available as a FastDigest enzyme for rapid DNA digestion. Isoschizomers: Ama87I, AvaI, BmeT110I, BsiHKCI, BsoBIm.
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 sent 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
规格
| Compatible Buffer: | 10x Buffer Tango |
|---|---|
| Enzyme: | Eco88I (AvaI) |
| Methylation Sensitivity: | CpG methylation-sensitive, Not dam methylation-sensitive, Not dcm methylation-sensitive |
| Optimal Reaction Temperature: | 37° C |
| Product Size: | 1,000 units |
| Sensitive to Heat Inactivation: | Yes |
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文献和实验Determining the Direction of Replication Fork Movement
without interference from nicked or broken DNA. As an example of the procedure, consider an XbaI restriction fragment that is replicated by a single replication fork and has an AvaI site near one end. The XbaI cleaved replication intermediates are separated by mass
DNA digestion and Southern blotting procedure for monocot DNA
DNA Digestion Make a cocktail as follows: Southern hybridization cocktail 10 X buffer 3.50 µL BSA [stock: 10 mg/mL
Salmon Sp.DNA 2ml Salmon Sp.DNA 2 ml Poly A 5µl Poly A µl 32cDNA probe 50-100µl (note: Salmon Sperm DNA stock is 5mg/ml; Poly A stock is 10mg/ml; make up prehyb and hyb sol'ns in 50ml conicals) 9) During prehybridization, label cDNA probe (purified
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