rpc53抗体rpc53兔多抗抗体DNA-directed
RNA polymerase III subunit rpc4 (RNA polymerase III subunit C4) (RNA polymerase III subunit C53) rpc53 rpc4 SPCC18.07抗体rpc53 Antibody抗体- ￥440 - 1320
- CUSABIO
- CN
- CSB-PA018346XA01SXV
- 2025年07月13日
- ELISA, WB; Recommended dilution: WB:1:500-1:5000
- Rabbit
- Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast)
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Recombinant Schizosaccharomyces pombe (Fission yeast) rpc53 protein (58-196)
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
Upon receipt, store at -20℃ or -80℃. Avoid repeated freeze.
- 克隆性：
Polyclonal
- 标记物：
Non-conjugated
- 适应物种：
Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast)
- 保质期：
6个月
- 抗原来源：
Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast)
- 目录编号：
O74857
- 级别：
优
- 库存：
200
- 供应商：
武汉华美生物工程有限公司
- 宿主：
Rabbit
- 应用范围：
ELISA, WB; Recommended dilution: WB:1:500-1:5000
- 浓度：
>95%,Protein G purified
- 靶点：
rpc53
- 抗体英文名：
rpc53 Antibody
- 抗体名：
DNA-directed RNA polymerase III subunit rpc4 (RNA polymerase III subunit C4) (RNA polymerase III subunit C53) rpc53 rpc4 SPCC18.07
- 规格：
100μl/50μl/20μl
| 规格： | 100μl | 产品价格： | ￥1320.0 |
|---|---|---|---|
| 规格： | 50μl | 产品价格： | ￥880.0 |
| 规格： | 20μl | 产品价格： | ￥440.0 |
保存缓冲液
Preservative: 0.03% Proclin 300Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
功能
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文献和实验An RNA Polymerase II In Vitro Transcription System
A great deal of attention in recent years has been focused on the mechanisms governing transcription. Repression and/or activation of specific genes, or sets of genes, represents a key regulatory step in such diverse processes as cell growth
Polycistronic Expression of Interfering RNAs from RNA Polymerase III Promoters
In many RNA silencing applications, there is a benefit to expressing multiple interfering RNAs simultaneously. This can be achieved by using a single RNA polymerase II promoter to express multiple micro(mi)RNA-formatted interfering RNAs
Assembly and Transcription of Chromatin Templates Using RNA Polymerase III
The use of in vitro model systems has been essential to the dissection of the mechanisms for transcription regulation. It is now possible to reconstitute specific transcription by each of the three eukaryotic RNA polymerases using purified
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