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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
FastDigest Bst1107I
- 供应商:
上海研卉生物
- 保存条件:
低温
- 库存:
大量
- 规格:
100 reactions
描述
| 5' | G | T | A ↓ | T | A | C | 3' | ||||
| 3' | C | A | T ↑ | A | T | G | 5' |
Thermo Scientific FastDigest Bst1107I restriction enzyme recognizes GTA^TAC site and cuts best at 37°C in 5–15 minutes using universal FastDigest Buffer. Isoschizomers: BstZ17I, BssNAI.
Thermo Scientific FastDigest Bst1107I 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: | Bst1107I |
| Methylation Sensitivity: | CpG methylation-sensitive, Not dam methylation-sensitive, Not dcm methylation-sensitive |
| Optimal Reaction Temperature: | 37° C |
| Product Line: | FastDigest |
| Product Size: | 100 reactions |
| Sensitive to Heat Inactivation: | No |
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nuclear RNA promoter-based parent vector using a single-stranded inverted repeat DNA and Bst DNA polymerase. The shRNA expression plasmids constructed by this method were confirmed to promote efficient RNA interference knockdown in silkworm cell lines
bst5 用pCDNA3.1-HIS载体做的重组,切去了一段含有终止密码子的片段,但下游仍有一个终止密码子,想请教一下是否影响目的蛋白的表达吗? sunyong_97 如果还有一个终止密码子,那么到那个位置肯定要终止的啊 bst5 可是终止密码子在我目的蛋白的下游啊,谢谢你的回复 sunyong_97 bst5 wrote:
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