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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
XmiI (AccI) (10 U/µL)
- 规格:
400 units
描述
| 5' | G | T ↓ | M | K | A | C | 3' | ||||
| 3' | C | A | K | M ↑ | T | G | 5' |
Thermo Scientific XmiI (AccI) restriction enzyme recognizes GT^MKAC sites and cuts best at 37°C in B 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: AccI, FblI.
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
规格
| Compatible Buffer: | 10x Buffer B |
|---|---|
| Enzyme: | XmiI (AccI) |
| Methylation Sensitivity: | CpG methylation-sensitive, Not dam methylation-sensitive, Not dcm methylation-sensitive |
| Optimal Reaction Temperature: | 37° C |
| Product Size: | 400 units |
| Sensitive to Heat Inactivation: | Yes |
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文献和实验8qoqdCv3RN/yazDp0Qt8JHmJhY+U5M19ZzQCif3ZkNE48HqYABNIEwRk8BfnGVlyIYtyCHy/u+K9qwf8QqJNTlUbBfTzI49WKn6EBbjD+TvNy7AGikbS0ESbKb9kAkwgBgKs+YgBCl9iAkwgtQjQsYsQPoI/YNfA6jh9xz10InnqYpzFGgyvkhOSuKFVCXNOV1LoJH89sMKSOecgPjRlgb/gcv8crv6sjvE7B8IkJrMThc6OB2MC6YsACx/pa794
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
平端连接通常情况下,PCR产物可直接与平端载体DNA进行连接,但其连接效 率效低。因为TaqDNA聚合酶具有非模板依赖性末端转移酶活性,能 在两6条DNA链的3'末端加上一个多余的碱基,使合成的PCR产物成为 3'突出一个碱基的DNA分子。这种DNA分子的连接效率很低。由于PCR 产物的效率通过较高,。在采用大量T4DNA连接酶并配以5-10u T4 RNA连接酶时,可显著提高其连接效率。对于较短PCR产物,用PUS19 的HincⅡ位点进行克隆,以X-gal和IPTG筛选,常可得到足量重组
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