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Mouse Monoclonal CD209 Antibody

  • 中文名: CD209抗体
  • 别    名: CDSIGN; CLEC4L; DC-SIGN; DC-SIGN1
货号: IPD31356
Price: ¥1280
数量:
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验证与应用

应用及物种
WB 1/500 - 1/2000 Human,Mouse,Rat
IF 咨询技术 Human,Mouse,Rat
IHC 咨询技术 Human,Mouse,Rat
ICC 技术咨询 Human,Mouse,Rat
FCM 1/200 - 1/400 Human,Mouse,Rat
Elisa 1/10000 Human,Mouse,Rat

产品详情

AliasesCDSIGN; CLEC4L; DC-SIGN; DC-SIGN1
Entrez GeneID30835
clone5C2A6
WB Predicted band size45.8kDa
Host/IsotypeMouse IgG1
Antibody TypePrimary antibody
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species ReactivityHuman
ImmunogenPurified recombinant fragment of human CD209 (AA: extra 270-404) expressed in E. Coli.
FormulationPurified antibody in PBS with 0.05% sodium azide

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参考文献

以下是关于CD209(DC-SIGN)抗体的3篇代表性文献及其简要摘要:

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1. **标题**:*DC-SIGN, a dendritic cell-specific HIV-1-binding protein that enhances trans-infection of T cells*

**作者**:Geijtenbeek, T.B., et al.

**摘要**:该研究首次揭示了DC-SIGN(CD209)在树突细胞介导的HIV-1传播中的关键作用。通过使用特异性抗体阻断实验,证明DC-SIGN与HIV-1包膜蛋白gp120结合,促进病毒向T细胞的转移,为靶向DC-SIGN的抗体治疗提供了理论基础。

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2. **标题**:*Structural basis for selective recognition of oligosaccharides by DC-SIGN and DC-SIGNR*

**作者**:Feinberg, H., et al.

**摘要**:通过X射线晶体学结合抗体表位分析,解析了DC-SIGN的碳水化合物识别结构域(CRD)与病原体糖基化蛋白的相互作用机制,揭示了抗体靶向CRD可抑制病原体(如埃博拉病毒)与宿主细胞的结合。

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3. **标题**:*DC-SIGN (CD209) mediates dengue virus infection of human dendritic cells*

**作者**:Tassaneetrithep, B., et al.

**摘要**:研究发现登革热病毒通过DC-SIGN感染人树突细胞,利用抗CD209抗体阻断实验证实该受体在病毒内吞中的必要性,为开发基于抗体或受体阻断的抗病毒策略提供了依据。

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4. **标题**:*Targeting DC-SIGN via its carbohydrate recognition domain for anti-HIV therapy*

**作者**:Svajger, U., et al.

**摘要**:该文献探讨了针对DC-SIGN碳水识别结构域(CRD)的单克隆抗体在抑制HIV-1与树突细胞结合中的应用,通过体外实验证明特定抗体可显著降低病毒捕获和转运效率,提示其治疗潜力。

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这些研究涵盖了CD209抗体的功能机制、结构基础及治疗应用方向。如需具体文献年份或期刊信息,可进一步补充检索关键词。

背景信息

CD209. also known as DC-SIGN (Dendritic Cell-Specific Intercellular adhesion molecule-3-Grabbing Non-integrin), is a C-type lectin receptor predominantly expressed on the surface of dendritic cells and macrophages. It plays a critical role in pathogen recognition, cell-cell interactions, and immune modulation by binding to high-mannose glycans on viral, bacterial, and fungal surfaces. CD209 antibodies are essential tools for studying its function in infectious diseases (e.g., HIV, Ebola, dengue), cancer immunology, and autoimmune disorders. These antibodies enable detection of CD209 expression in tissues or cells, block ligand-receptor interactions, or modulate immune responses. Research highlights its dual role: promoting pathogen uptake for immune surveillance while being exploited by pathogens for immune evasion. CD209-targeting therapies, including antibody-based strategies, are explored for vaccine development and immunotherapies. Structural studies reveal its carbohydrate-recognition domain (CRD) and cytoplasmic tail as key functional regions. Antibody specificity varies, with some recognizing conserved epitopes across species, aiding translational research. Challenges include understanding context-dependent signaling and avoiding off-target effects in therapeutic applications.

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