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- Prospecbio
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- ant-589
- 2025年07月17日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
for future use below -18°C
- 保质期：
See instructions
- 英文名：
FUBP1
- 库存：
常规产品有备货
- 供应商：
上海经科化学科技有限公司
- CAS号：
无
- 规格：
5ug/20ug/100ug
| 规格： | 5ug | 产品价格： | ￥1080.0 |
|---|---|---|---|
| 规格： | 20ug | 产品价格： | ￥2415.0 |
| 规格： | 100ug | 产品价格： | ￥7500.0 |
CATALOGUE NUMBER
ANT-589
SYNONYMS
TYPE
INTRODUCTION
FUBP1 is a ssDNA binding protein which stimulates expression of c-myc in undifferentiated cells and activates the far upstream element (FUSE) of c-myc. Regulation of FUSE by FUBP happens by single-strand binding of FUBP to the non-coding strand. FUBP1 performs as an ATP-dependent DNA helicase.
CLONE
PHYSICAL APPEARANCE
IMMUNOGEN
IG SUBCLASS
PURIFICATION METHOD
FORMULATION
1mg/ml containing PBS, pH-7.4, 10% Glycerol and 0.02% Sodium Azide.
STORAGE PROCEDURES
STABILITY / SHELF LIFE
APPLICATIONS
FUBP1 antibody has been tested by ELISA, Western blot and ICC/IF analysis to assure specificity and reactivity. Since application varies, however, each investigation should be titrated by the reagent to obtain optimal results. Recommended starting dilution for Western blot analysis is 1:1000.
SAFETY DATA SHEET
SDS
USAGE
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文献和实验FUBP1 is a ssDNA binding protein which stimulates expression of c-myc in undifferentiated cells and activates the far upstream element (FUSE) of c-myc. Regulation of FUSE by FUBP happens by single-strand binding of FUBP to the non-coding strand. FUBP1 performs as an ATP-dependent DNA helicase.
Purification of the human TATA-Binding Protein, TBP
The TATA-binding protein TBP plays a central role in eukaryotic transcription initiation (1 , 2 ). TBP binds to the promoter consensus sequence TATAAA, located approx 30 nucleotides upstream of the transcriptional start site. Once bound, TBP
Identification of Protein Interactions by Far Western Analysis
far western blotting, a method of identifying protein?protein interactions. In a far western blot, one protein of interest is immobilized on a solid support membrane, then probed with a non?antibody protein. As described, far western blots can be used
process, transferred proteins generally renature with greater efficiency and are therefore more easily detected by far-Western blotting. In the event that the protein is unable to re-fold to create an intact binding site, it may be necessary to add
技术资料