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- 英文名:
FastDigest XhoI
- 规格:
400 reactions
描述
| 5' | C ↓ | T | C | G | A | G | 3' | ||||
| 3' | G | A | G | C | T ↑ | C | 5' |
Thermo Scientific FastDigest XhoI restriction enzyme recognizes C^TCGAG site and cuts best at 37°C in 5–15 minutes using universal FastDigest Buffer. Isoschizomers: PaeR7I, Sfr274I, SlaI, StrI, TliI.
Thermo Scientific FastDigest XhoI is one of an advanced line of fast restriction enzymes that are all 100% active in the universal FastDigest and FastDigest Green reaction buffers.
The universal buffer allows rapid single-, double-, or multiple DNA digestion within 5–15 minutes eliminating any need for buffer change or subsequent DNA clean-up steps. See Reaction Conditions for FastDigest Enzymes for a table of enzyme activity, heat inactivation and incubation times for this and other FastDigest restriction enzymes. DNA modifying enzymes, such as Klenow Fragment, T4 DNA Ligase, alkaline phosphatases and T4 DNA Polymerase all have 100% activity in FastDigest Buffer. Therefore, enzymes for downstream applications can be directly added to the FastDigest reaction mix.
For additional convenience FastDigest Green Buffer includes a density reagent and two tracking dyes for direct loading of digestion reaction products on gels.
Short incubation times and optimal composition of the universal FastDigest Buffer eliminate star activity effects.
Features
• 100% activity of all FastDigest enzymes in the universal buffer
• 100% buffer compatibility with downstream applications
规格
| Compatible Buffer: | 10x FastDigest Buffer/FastDigest Green Buffer |
|---|---|
| Enzyme: | Xho I |
| Methylation Sensitivity: | CpG methylation-sensitive, Not dam methylation-sensitive, Not dcm methylation-sensitive |
| Optimal Reaction Temperature: | 37° C |
| Product Line: | FastDigest |
| Product Size: | 400 reactions |
| Sensitive to Heat Inactivation: | Yes |
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文献和实验jing1209 HR includes gene conversion of the XhoI site without an associated crossover or deletion of one GFP copy by crossover or single-strand annealing. 非常感谢!!! LoftyMan HR是不包括主动交换的相关基因交换或单GFP拷贝缺失,也是不包括单链
Burnell pBT载体多克隆位点酶切:见附件 由于酶切位点离得近,用NotI 和 XhoI 是否能同时进行双酶切,还是需要分部酶切? 另外,分别含 NotI和XhoI酶切位点的修饰引物一般需要几个保护碱基? Burnell 期待各位朋友为我答疑解惑,最近实验很郁闷,很悲剧! angler5156 不知道你用的什么公司的酶进行酶切
常见限制性内切酶识别序列(酶切位点)(BamHI、EcoRI、HindIII、NdeI、XhoI等) 在分子克隆实验中,限制性内切酶是必不可少的工具酶。 无论是构建克隆载体还是表达载体,要根据载体选择合适的内切酶(当然,使用T载就不必考虑了)。先将引物设计好,然后添加酶切识别序列到引物5' 端。常用的内切酶比如BamHI、EcoRI、HindIII、NdeI
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