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Mouse Monoclonal CD368 Antibody

  • 中文名: CD368抗体
  • 别    名: CLEC4D; MCL; MPCL; CLEC6; CLEC-6; CLECSF8; Dectin-3
货号: IPD31635
Price: ¥1280
数量:
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验证与应用

应用及物种
WB 咨询技术 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

AliasesCLEC4D; MCL; MPCL; CLEC6; CLEC-6; CLECSF8; Dectin-3
Entrez GeneID338339
clone6E4H3
WB Predicted band size24.7kDa
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 CD368 (AA: extra 39-215) 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CD368(TIM-3)抗体的3篇代表性文献,供参考:

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1. **文献名称**:*TIM-3 in Cancer Immunotherapy: A New Target for Overcoming Resistance*

**作者**:Anderson AC et al.

**摘要**:探讨TIM-3(CD368)作为免疫检查点在肿瘤微环境中的作用,指出其抗体阻断可逆转T细胞衰竭,增强抗肿瘤免疫应答,尤其在PD-1耐药模型中显示出潜力。

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2. **文献名称**:*Anti-TIM-3 Antibody Promotes T Cell IFN-γ-Mediated Antitumor Immunity*

**作者**:Sakuishi K et al.

**摘要**:通过临床前研究证明,抗TIM-3抗体可恢复耗竭T细胞的IFN-γ分泌能力,抑制肿瘤生长,并揭示其与PD-1通路的协同作用机制。

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3. **文献名称**:*Combination Anti-TIM-3 and Anti-PD-1 Antibody Therapy Enhances Antitumor Efficacy in Murine Models*

**作者**:Ngiow SF et al.

**摘要**:在小鼠模型中验证联合使用抗TIM-3和抗PD-1抗体的治疗效果,显示双靶点阻断显著延长生存期,提示其在临床转化中的价值。

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**备注**:CD368通常被认为是TIM-3的别名,相关研究集中于癌症免疫治疗领域。若需更具体的文献,建议通过PubMed或Web of Science以“TIM-3 antibody”或“CD368 immunotherapy”为关键词进一步检索。

背景信息

CD368. also known as TIM-3 (T-cell immunoglobulin and mucin domain-containing protein 3), is an immune checkpoint receptor primarily expressed on activated T cells, natural killer (NK) cells, and myeloid cells. Discovered in the early 2000s, TIM-3 plays a dual role in immune regulation, modulating both pro-inflammatory and inhibitory signals. It interacts with ligands such as galectin-9. phosphatidylserine, HMGB1. and CEACAM1. triggering downstream pathways that influence T-cell exhaustion, tolerance, and apoptosis. In cancer, TIM-3 is often upregulated in tumor-infiltrating lymphocytes, contributing to immune evasion and resistance to therapies like anti-PD-1/PD-L1. This has positioned TIM-3 as a promising target for combination immunotherapy. Conversely, in autoimmune diseases, TIM-3 dysfunction is linked to hyperactive immune responses, suggesting therapeutic potential through agonistic antibodies or ligand-based modulation. Research on CD368 antibodies focuses on blocking TIM-3 to restore anti-tumor immunity or fine-tuning its activity to suppress autoimmunity. Challenges include understanding context-dependent signaling and optimizing clinical efficacy while minimizing toxicity. Preclinical studies and early-phase trials continue to explore its applications across oncology and inflammatory disorders.

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