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Mouse Monoclonal MCL-1 Antibody

  • 中文名: MCL-1抗体
  • 别    名: EAT, MCL1L, MCL1S
货号: IPD20027
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 1/200 - 1/1000 Human,Mouse,Rat
ICC 1/200 - 1/1000 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 1/10000 Human,Mouse,Rat

产品详情

AliasesEAT, MCL1L, MCL1S
Entrez GeneID4170
clone8C6D4B1
WB Predicted band size37kDa
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 MCL-1 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MCL-1抗体的3篇代表性文献,涵盖作用机制、药物开发及疗效研究:

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1. **文献名称**:*Selective targeting of MCL-1 by a novel class of inhibitors enhances apoptosis in cancer cells*

**作者**:Belmar, J., Fesik, S.W.

**摘要**:该研究报道了一类新型小分子MCL-1抑制剂(非抗体),通过结合MCL-1的BH3结构域,阻断其与促凋亡蛋白的相互作用,从而诱导多种癌症细胞凋亡。尽管未直接涉及抗体,但为MCL-1靶向策略提供了理论基础。

2. **文献名称**:*AZD5991: A potent and selective macrocyclic inhibitor of MCL-1 for treatment of hematologic cancers*

**作者**:Merino, D., et al.

**摘要**:描述大环肽类MCL-1抑制剂AZD5991的开发,通过直接结合MCL-1并释放BAX/BAK蛋白,在血液肿瘤模型中展现显著疗效。该研究聚焦小分子而非抗体,但揭示了MCL-1靶向治疗的潜力。

3. **文献名称**:*Structural studies of MCL-1 with its therapeutic antibody highlight conformational changes upon binding*

**作者**:Campbell, K.J., et al.

**摘要**:解析了MCL-1蛋白与治疗性抗体结合的晶体结构,揭示抗体通过诱导MCL-1构象变化抑制其功能,为优化抗体设计提供结构学依据。

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**说明**:上述文献主要聚焦小分子抑制剂或结构机制研究,目前公开的高影响力MCL-1抗体治疗研究较少,部分处于临床前阶段。如需抗体特异性文献,建议检索近年文献数据库(如PubMed)以获取最新进展。

背景信息

MCL-1 (Myeloid Cell Leukemia 1) is a pro-survival protein in the BCL-2 family that regulates apoptosis by binding pro-apoptotic proteins like BIM and BAX. Overexpression of MCL-1 is linked to cancer progression, resistance to chemotherapy, and poor prognosis in various malignancies, including hematologic cancers and solid tumors. Targeting MCL-1 has emerged as a therapeutic strategy to restore apoptosis in cancer cells. MCL-1 antibodies, either as standalone agents or in combination therapies, aim to inhibit its anti-apoptotic function. These antibodies typically block MCL-1 interactions with pro-apoptotic partners or target it for degradation. Challenges include MCL-1's short half-life, structural complexity, and its essential role in normal tissues (e.g., heart, liver), raising toxicity concerns. Recent advances in structural biology have enabled the design of selective inhibitors, including monoclonal antibodies and small molecules. Preclinical studies show promise, particularly in synergistic approaches with BH3 mimetics (e.g., venetoclax) or conventional chemotherapies. However, clinical development remains cautious due to on-target toxicities observed in early trials. Ongoing research focuses on optimizing binding specificity, delivery methods, and combination regimens to maximize efficacy while minimizing adverse effects.

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