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Rabbit Monoclonal ATP6V0D1 Antibody

  • 中文名: ATP6V0D1抗体
  • 别    名: P39; VATX; VMA6; ATP6D; ATP6DV; VPATPD
货号: IPDX21098
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 1/20 Human,Mouse,Rat
IHC 1/50-1/100 Human,Mouse,Rat
ICC 1/50-1/200 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 咨询技术 Human,Mouse,Rat

产品详情

AliasesP39; VATX; VMA6; ATP6D; ATP6DV; VPATPD
Entrez GeneID9114
WB Predicted band sizeCalculated MW: 40 kDa; Observed MW: 40 kDa
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,Mouse,Rat
ImmunogenRecombinant protein of human ATP6V0D1
FormulationPurified antibody in TBS with 0.05% sodium azide,0.05%BSA and 50% glycerol.

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参考文献

以下是关于ATP6V0D1抗体的参考文献示例(内容为模拟示例,仅供参考):

1. **《ATP6V0D1调控溶酶体酸化促进乳腺癌细胞侵袭》**

*作者:Zhang Y, et al.*

摘要:研究通过ATP6V0D1抗体检测发现,该蛋白在乳腺癌中高表达,并通过调节溶酶体酸化促进肿瘤细胞侵袭,为癌症治疗提供潜在靶点。

2. **《V-ATP酶亚基ATP6V0D1在神经炎症中的作用》**

*作者:Li X, et al.*

摘要:利用ATP6V0D1抗体进行免疫荧光染色,揭示其在小胶质细胞中调控溶酶体功能,参与神经炎症反应,可能与阿尔茨海默病相关。

3. **《ATP6V0D1缺失导致自噬障碍的分子机制》**

*作者:Wang J, et al.*

摘要:研究通过Western blot(ATP6V0D1抗体验证)发现,该蛋白缺失会抑制自噬体-溶酶体融合,导致细胞代谢异常,影响疾病进展。

4. **《ATP6V0D1作为肾细胞癌诊断标志物的研究》**

*作者:Chen L, et al.*

摘要:通过组织芯片结合ATP6V0D1抗体免疫组化分析,证实其过表达与肾癌患者预后不良相关,提示其临床诊断价值。

注:以上为模拟文献,实际引用请通过学术数据库(如PubMed、Web of Science)检索具体研究。

背景信息

The ATP6V0D1 antibody is a tool used to detect the ATP6V0D1 protein, a subunit of the vacuolar-type H+-translocating ATPase (V-ATPase) complex. V-ATPases are proton pumps critical for acidifying intracellular organelles like lysosomes, endosomes, and secretory vesicles, thereby maintaining pH gradients essential for processes such as protein degradation, membrane trafficking, and synaptic transmission. The ATP6V0D1 subunit, part of the V0 domain, plays a structural role in V-ATPase assembly and proton translocation. Research on ATP6V0D1 focuses on its involvement in cellular homeostasis, autophagy, and diseases like cancer, neurodegenerative disorders, and osteoporosis. In cancer, V-ATPases are linked to tumor metastasis and drug resistance, with ATP6V0D1 overexpression observed in certain malignancies. In neurodegeneration, dysfunctional lysosomal acidification due to V-ATPase defects contributes to pathologies like Alzheimer’s and Parkinson’s diseases. ATP6V0D1 antibodies are utilized in techniques such as Western blotting, immunofluorescence, and immunohistochemistry to study protein expression, localization, and regulation across tissues and disease models. These antibodies are crucial for elucidating ATP6V0D1’s role in cellular physiology and its potential as a therapeutic target. Validation of antibody specificity, often via knockout controls or peptide blocking, ensures accurate detection, minimizing cross-reactivity with related V-ATPase subunits.

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