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Mouse Monoclonal CD299 Antibody

  • 中文名: CD299抗体
  • 别    名: CLEC4M; LSIGN; CD209L; L-SIGN; DCSIGNR; HP10347; DC-SIGN2; DC-SIGNR
货号: IPD31626
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

AliasesCLEC4M; LSIGN; CD209L; L-SIGN; DCSIGNR; HP10347; DC-SIGN2; DC-SIGNR
Entrez GeneID10332
clone8A1B3
WB Predicted band size45.4kDa
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 CD299 (AA: extra 237-399) 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CD299(DC-SIGNR/L-SIGN)抗体的3篇参考文献及其摘要内容:

1. **"DC-SIGNR: A novel HIV-1-binding C-type lectin that mediates trans-infection of T cells"**

- **作者**: Alvarez CP, et al.

- **摘要**: 该研究揭示了DC-SIGNR(CD299)作为C型凝集素受体在HIV-1感染中的作用,证明其通过结合病毒表面糖蛋白gp120介导病毒向T细胞的传递,并发现抗CD299抗体可阻断这一过程。

2. **"Ebola virus glycoprotein binding to DC-SIGNR: A mechanism of immune evasion?"**

- **作者**: Lozach PY, et al.

- **摘要**: 研究发现埃博拉病毒糖蛋白与CD299受体结合,促进病毒进入宿主细胞,并提示病毒可能通过此途径逃避免疫监测。抗CD299抗体可显著抑制病毒与宿主细胞的相互作用。

3. **"Tissue-specific regulation of immune responses by DC-SIGNR isoforms"**

- **作者**: Soilleux EJ, et al.

- **摘要**: 通过抗CD299抗体的免疫组化分析,揭示了DC-SIGNR在肝脏、淋巴结等组织的内皮细胞中高表达,并探讨其不同亚型在调节病原体识别和免疫耐受中的功能差异。

4. **"Targeting CLEC4M (DC-SIGNR) for antiviral therapy: Insights from antibody-based inhibition"**

- **作者**: Zhang Y, et al.

- **摘要**: 研究评估了抗CD299抗体在阻断HCV和SARS-CoV假病毒感染中的效果,证明其具有开发为广谱抗病毒药物的潜力,并分析了抗体表位与抑制效率的关系。

以上文献均聚焦于CD299在病原体感染中的生物学功能及抗体干预策略。

背景信息

CD299. also known as CLEC4M or L-SIGN (Liver/lymph node-Specific ICAM-3 Grabbing Non-integrin), is a C-type lectin receptor primarily expressed on liver sinusoidal endothelial cells and lymph node endothelial cells. It plays a role in pathogen recognition, immune regulation, and cell adhesion by binding high-mannose glycans on viral envelopes and bacterial surfaces. CD299 interacts with pathogens such as HIV, Ebola, hepatitis C virus (HCV), and Mycobacterium tuberculosis, facilitating their capture and presentation to immune cells. Structurally, it contains a carbohydrate recognition domain (CRD) critical for glycan binding and a transmembrane region enabling signal transduction. Antibodies targeting CD299 are valuable tools for studying its role in infections, immune tolerance, and inflammatory diseases. They help elucidate mechanisms of pathogen entry, immune evasion, and potential therapeutic interventions. Additionally, CD299 antibodies have diagnostic applications, such as detecting receptor expression in tissues or blocking pathogen-receptor interactions in experimental models. Research also explores their utility in vaccine development and targeted therapies, particularly for liver-tropic infections. Understanding CD299’s dual role in immunity and infection continues to drive antibody-based research in infectious and autoimmune diseases.

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