- ￥1700 - 4000
- GeneTex
- 美国
- GTX103343
- 2025年07月16日
- WB, ICC/IF, FACS
- Rabbit
- Dengue virus
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Carrier-protein conjugated synthetic peptide encompassing a sequence within the N-terminus region of Dengue virus Capsid protein (Dengue virus 2 (strain 16681 PDK 53)). The exact sequence is proprietary.
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
- 克隆性：
Polyclonal
- 标记物：
Unconjugated
- 适应物种：
Dengue virus
- 保质期：
12 months from the shipping date of the product.
- 抗原来源：
Dengue virus 2
- 目录编号：
GTX103343
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Rabbit
- 应用范围：
WB, ICC/IF, FACS
- 浓度：
0.16 mg/ml (Please refer to the vial label for the specific concentration.)
- 靶点：
Dengue virus Capsid protein
- 抗体英文名：
Dengue virus Capsid protein antibody
- 抗体名：
Dengue virus Capsid protein 抗体
- 规格：
100 μl/25 μl
| 规格： | 100 μl | 产品价格： | ￥4000.0 |
|---|---|---|---|
| 规格： | 25 μl | 产品价格： | ￥1700.0 |
Non-infected (–) and infected (+) BHK-21 whole cell extracts (30 μg) were separated by 15% SDS-PAGE, and the membrane was blotted with Dengue virus Capsid protein antibody (GTX103343) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.
GTX103343 IF Image Immunofluorescence analysis of Denque virus 2-infected BHK-21, using Capside Protein (Dengue virus 2 ) antibody (GTX103343) at 1:2000 dilution.
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文献和实验Utomo DIS et al., AMB Express 2022 (PMID:35102445)
Liu B et al., Virol Sin 2020 (PMID:33044659)
Li LH et al., Antiviral Res 2020 (PMID:32898584)
Butler, M et al., Viruses 2020 (PMID:32560467)
Li M et al., Nat Microbiol 2019 (PMID:30833725)
Ngo AM et al., Elife 2019 (PMID:31516121)
Cortese M et al., Cell Rep 2019 (PMID:31141684)
Kao JC et al., PLoS Negl Trop Dis 2018 (PMID:30125275)
Juan Fidel Osuna-Ramos et al., bioRxiv 2018 (Epub)
Roth H et al., MBio 2017 (PMID:28074025)
Perry JW et al., J Virol 2018 (PMID:29321321)
Reyes-Ruiz JM et al., Virology 2017 (PMID:29272748)
Campos RK et al., J Virol 2016 (PMID:27974556)
Angel-Ambrocio AH et al., Virus Res 2015 (PMID:25598317)
Wu Y et al., Front Microbiol 2022 (PMID:35865923)
Shen TJ et al., JCI Insight 2022 (PMID:36125898)
Shwetha Shivaprasad et al., PLoS Pathog 2022 (PMID:35482886)
against dengue, timely diagnosis is therefore necessary for patient management. Laboratory diagnosis is carried out by virus isolation, demonstration of viral antigen, presence of viral nucleic acid, and antibodies. Further, recombinant dengue envelope protein
The Identification of Dengue Virus Using PCR
of a genome RNA and capsid (C) proteins. The virion structure is easily destroyed by treatment with non-ionic detergent ( see Fig. 1 ) or low osmotic shock. Four antigenically related but distinct serotypes of dengue virus (DEN1, DEN2, DEN3, and DEN
Tobacco Mosaic Virus Capsid Protein as Targets for the Self-Assembly of Gold Nanoparticles
of naturally evolved systems to produce highly organized assemblies of small molecules and nanoparticles. Here we describe a method whereby arginine residues on a viral coat protein (Tobacco Mosaic Virus) are targeted by bis(p -sulfonatophenyl)phenylphosphine
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