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Rabbit Polyclonal ATP6V1C2 Antibody

  • 中文名: ATP6V1C2抗体
  • 别    名: Vacuolar proton pump subunit C 2; V-ATPase subunit C 2; ATP6V1C2;
货号: IPDX42659
Price: ¥1180
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 咨询技术 Human,Mouse,Rat
Elisa 咨询技术 Human,Mouse,Rat

产品详情

AliasesVacuolar proton pump subunit C 2; V-ATPase subunit C 2; ATP6V1C2;
Entrez GeneID245973;
WB Predicted band size49kDa
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
ImmunogenSynthesized peptide derived from internal of human ATP6V1C2.
FormulationPurified antibody in PBS with 0.05% sodium azide.

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参考文献

以下是关于ATP6V1C2抗体的3篇参考文献示例(注:以下内容为模拟生成,实际文献需通过学术数据库检索确认):

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1. **文献名称**:*ATP6V1C2 regulates osteoclast differentiation and bone resorption via modulating NF-κB signaling*

**作者**:Li Y, et al.

**摘要**:本研究通过免疫组化和Western blot分析,利用特异性ATP6V1C2抗体,揭示了该蛋白在破骨细胞分化中的关键作用。实验表明,ATP6V1C2通过调控NF-κB通路影响骨吸收功能,为骨质疏松治疗提供了潜在靶点。

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2. **文献名称**:*ATP6V1C2 as a prognostic biomarker in head and neck squamous cell carcinoma*

**作者**:Wang X, et al.

**摘要**:研究者使用商业化ATP6V1C2抗体对临床样本进行染色,发现该蛋白在头颈鳞癌中高表达且与患者生存率负相关。进一步功能实验证实其通过酸化微环境促进肿瘤侵袭,提示其作为预后标志物的潜力。

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3. **文献名称**:*Characterization of a novel polyclonal antibody against human ATP6V1C2 subunit*

**作者**:Zhang R, et al.

**摘要**:本文报道了一种新型ATP6V1C2多克隆抗体的开发与验证。通过免疫印迹和免疫荧光实验,证明该抗体特异性识别内源性及外源性ATP6V1C2蛋白,适用于多种细胞模型的亚细胞定位研究。

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**注意事项**:

- 实际文献需通过PubMed、Google Scholar等平台以关键词“ATP6V1C2 antibody”或“V-ATPase C2 subunit”检索,并筛选涉及抗体应用的研究。

- 部分研究可能未在标题/摘要中直接提及“抗体”,需结合方法学部分确认。

- 近年研究偏向于ATP6V1C2在癌症、神经疾病及代谢异常中的作用机制探索。

建议补充具体需求(如应用领域或物种),以便提供更精准的文献支持。

背景信息

The ATP6V1C2 antibody is a research tool targeting the ATP6V1C2 protein, a subunit of the vacuolar-type H+-ATPase (V-ATPase) complex. V-ATPases are evolutionarily conserved proton pumps that acidify intracellular compartments (e.g., lysosomes, endosomes) and regulate extracellular pH in certain tissues. The ATP6V1C2 subunit, part of the V1 domain, facilitates ATP hydrolysis and participates in assembly/regulation of the complex. It is one of two isoforms (C1 and C2) encoded by distinct genes, with C2 showing tissue-specific expression in organs like the kidney, liver, and reproductive tissues. Dysregulation of ATP6V1C2 has been implicated in pathological processes, including cancer progression, where its overexpression correlates with metastasis, drug resistance, and poor prognosis in breast, prostate, and ovarian cancers. Antibodies against ATP6V1C2 are used to study its expression patterns, subcellular localization, and functional roles via techniques like Western blotting, immunohistochemistry, and immunofluorescence. These tools help elucidate its contribution to pH-dependent processes such as protein degradation, membrane trafficking, and bone resorption. Recent studies also explore ATP6V1C2 as a potential therapeutic target, particularly in cancers reliant on V-ATPase activity for survival. Validation of antibody specificity through knockout controls or siRNA knockdown is critical due to structural homology between C1 and C2 isoforms.

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