Anti-SEBOV RNA-directed RNA po
lymerase L/Protein L Nanobody (SAA1489), 抗SEBOV RNA-directed RNA polymerase L/Protein L纳米抗体 (SAA1489)- ￥1338
- abinscience
- France
- VK591013
- 2026年03月03日
- Sudan ebolavirus (strain Human/Uganda/Gulu/2000) (SEBOV) (Sudan Ebolavirus)
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- 文献和实验
- 技术资料
- 亚型：
VHH-8His-Cys-tag
- 形态：
Liquid
- 保存条件：
0.01M PBS, pH 7.4.
- 克隆性：
Monoclonal
- 适应物种：
Sudan ebolavirus (strain Human/Uganda/Gulu/2000) (SEBOV) (Sudan Ebolavirus)
- 保质期：
1 year
- 抗原来源：
Alpaca
- 目录编号：
VK591013
- 级别：
科研级别
- 库存：
999
- 供应商：
abinscience
- 浓度：
1mg/ml
- 抗体英文名：
Anti-SEBOV RNA-directed RNA polymerase L/Protein L Nanobody (SAA1489)
- 抗体名：
Anti-SEBOV RNA-directed RNA polymerase L/Protein L Nanobody (SAA1489)
- 规格：
50ug
| Product name | Anti-SEBOV RNA-directed RNA polymerase L/Protein L Nanobody (SAA1489) |
|---|---|
| Catalog No. | VK591013 |
| Host species | Alpaca |
| Specificity | \ |
| Conjugation | \ |
| Species reactivity | Sudan ebolavirus (strain Human/Uganda/Gulu/2000) (SEBOV) (Sudan Ebolavirus) |
| Immunogen | \ |
| Form | Liquid |
| Storage buffer | 0.01M PBS, pH 7.4. |
| Purity | >95% as determined by SDS-PAGE. |
| Clonality | Monoclonal |
| Isotype | VHH-8His-Cys-tag |
| Applications | ELISA |
| Target | L, RNA-directed RNA polymerase L, Protein L, Large structural protein, Replicase, Transcriptase |
| Purification | Purified by Nickel column. |
| Accession | Q5XX01 |
| Stability and Storage | Use a manual defrost freezer and avoid repeated freeze-thaw cycles. Store at 4°C short term (1-2 weeks). Store at -20°C 12 months. Store at -80°C long term. |
| Background | \ |
| Alternative Names | \ |
| Clone ID | SAA1489 |
| Species | \ |
| Note | For research use only. |
Abinscience, founded in 2023 and located in the innovation technology center in Strasbourg, France, is the core research reagent brand of ProteoGenix. Focusing on the development and production of life science research reagents, Abinscience takes "Empowering Bioscience Discovery" as its vision, and is committed to providing high-quality and innovative biological reagent products and technical solutions for global researchers.
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文献和实验in 100µl of elution buffer at 65°C for 5 minutes;7.The eluted complexes can then be electrophoresed in denaturing PAGE and subjected to western blot analysis with an anti-Flag antibody for detection of the particular flag-tagged protein of choice (Figure
mRNA Amplification with T7 RNA Polymerase
RNase H Vortex master mix briefly, pull down by spinning briefly and place on ice. Add 80 µL 2nd Strand Master Mix to each RNA sample. Mix by pipetting, flicking and spin briefly to pull down. Incubate RNA at 16ºC x 2 hrs on PCR
一、文献 1. Chen, H.H., J. Lebon, and A.D. Riggs, Analysis of RNA structure and RNA-protein interactions in mammalian cells by use of terminal transferase-dependent PCR. Methods Mol Biol, 2008. 488: p. 319-41. 2. Terzi, L.C. and G.G. Simpson
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