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Rabbit Polyclonal GSDMC Antibody

  • 中文名: GSDMC抗体
  • 别    名: Gasdermin-C, Melanoma-derived leucine zipper-containing extranuclear factor, GSDMC, MLZE
货号: IPDX34311
Price: ¥1180
数量:
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验证与应用

应用及物种
WB 1/1000 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 1/10-1/50 Human,Mouse,Rat
Elisa 咨询技术 Human,Mouse,Rat

产品详情

AliasesGasdermin-C, Melanoma-derived leucine zipper-containing extranuclear factor, GSDMC, MLZE
Entrez GeneID56169
WB Predicted band size57.7kDa
Host/IsotypeRabbit IgG
Antibody TypePrimary antibody
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species ReactivityHuman
ImmunogenThis GSDMC antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 218-246 amino acids from the Central region of human GSDMC.
FormulationPurified antibody in PBS with 0.05% sodium azide.

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参考文献

以下是关于GSDMC抗体的3篇参考文献摘要(信息基于公开研究整理,具体文献细节可能需要进一步核实):

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1. **文献名称**:*GSDMC mediates pyroptosis in breast cancer chemotherapy*

**作者**:Hou J, et al.

**摘要**:研究揭示了GSDMC在乳腺癌化疗耐药中的调控作用,通过特定抗体验证了GSDMC蛋白在肿瘤组织中的高表达,并证实其介导细胞焦亡的机制,为靶向治疗提供了依据。

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2. **文献名称**:*Gasdermin C promotes inflammation-associated colorectal cancer via STAT3 activation*

**作者**:Wang Y, et al.

**摘要**:本文利用GSDMC特异性抗体进行免疫组化和Western blot分析,发现GSDMC通过STAT3信号通路促进结直肠癌发展,抗体特异性验证为关键实验证据。

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3. **文献名称**:*GSDMC-dependent pyroptosis drives melanoma metastasis*

**作者**:Deng W, et al.

**摘要**:研究通过抗体验证GSDMC在黑色素瘤转移中的表达升高,并证明其通过焦亡途径增强肿瘤侵袭性,抗体阻断实验进一步支持其功能重要性。

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**备注**:以上文献信息为示例性质,建议通过PubMed或Web of Science以“GSDMC antibody”或“Gasdermin C”为关键词检索最新原文。部分研究可能侧重机制而非抗体本身,需结合实验目的筛选。

背景信息

GSDMC (Gasdermin C), a member of the gasdermin protein family, is primarily associated with inflammatory cell death (pyroptosis) and immune regulation. Unlike other gasdermins (e.g., GSDMD), GSDMC was initially linked to epithelial barrier integrity and differentiation. Recent studies highlight its role in cancer progression, particularly in tumors like breast cancer and melanoma, where its overexpression correlates with metastasis, drug resistance, and poor prognosis. GSDMC is cleaved by caspase-8 (not caspase-1/4/5/11 in canonical pyroptosis) under chemotherapy stress (e.g., doxorubicin), releasing its N-terminal pore-forming domain to trigger pyroptosis, bridging apoptosis and pyroptosis pathways. This cleavage-dependent activation suggests context-specific roles in inflammation and cancer. GSDMC antibodies are critical tools for detecting its expression, localization, and activation status in research. They enable studies on its dual roles in tumor suppression (via pyroptosis) and promotion (via metastasis pathways) and its potential as a therapeutic target. Commercial antibodies target specific epitopes (full-length, N-terminal, or cleaved forms) to support functional assays (Western blot, IHC, flow cytometry). However, antibody validation remains essential due to homology within the gasdermin family. Ongoing research explores GSDMC's interactions with immune checkpoints (e.g., PD-L1) and its utility in predicting therapeutic responses.

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