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Rabbit Polyclonal FNDC3B Antibody

  • 中文名: FNDC3B抗体
  • 别    名: FAD104; PRO4979; YVTM2421
货号: IPDX09039
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 1/25-1/100 Human,Mouse,Rat
ICC 技术咨询 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 1/5000-1/10000 Human,Mouse,Rat

产品详情

AliasesFAD104; PRO4979; YVTM2421
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
ImmunogenFull length fusion protein
FormulationPurified antibody in PBS with 0.05% sodium azide and 50% glycerol.

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参考文献

以下是关于FNDC3B抗体的模拟参考文献示例(仅供参考,非真实文献):

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1. **文献名称**:*FNDC3B promotes hepatocellular carcinoma metastasis via EMT regulation*

**作者**:Zhang Y, et al.

**摘要**:该研究通过Western blot和免疫组化实验,使用FNDC3B抗体检测其在肝细胞癌组织中的表达,发现FNDC3B通过激活EMT(上皮-间质转化)信号通路,显著促进肿瘤细胞的侵袭和转移。

2. **文献名称**:*FNDC3B as a prognostic biomarker in breast cancer progression*

**作者**:Wang L, et al.

**摘要**:作者利用FNDC3B特异性抗体分析乳腺癌患者组织样本,发现FNDC3B高表达与不良预后相关,可能通过调节细胞外基质重塑影响肿瘤微环境。

3. **文献名称**:*Mechanistic insights into FNDC3B-mediated Wnt signaling in colorectal cancer*

**作者**:Liu X, et al.

**摘要**:研究通过免疫荧光和Co-IP实验(使用FNDC3B抗体),揭示FNDC3B与Wnt/β-catenin通路相互作用,促进结肠癌细胞迁移,提示其作为潜在治疗靶点。

4. **文献名称**:*FNDC3B expression in stromal cells correlates with tumor angiogenesis*

**作者**:Chen R, et al.

**摘要**:利用FNDC3B抗体对多种癌症的基质细胞进行分析,发现其高表达与血管生成标志物(如VEGF)正相关,表明其在肿瘤血管形成中的调控作用。

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**注**:以上内容为模拟示例,实际文献需通过PubMed、Google Scholar等平台检索确认。若需真实文献,建议结合关键词“FNDC3B antibody”“FNDC3B function”或“FNDC3B cancer”进一步查询。

背景信息

The FNDC3B antibody targets the Fibronectin type III domain-containing protein 3B (FNDC3B), a transmembrane or secreted protein characterized by multiple fibronectin III (FN3) domains. FNDC3B is implicated in cellular adhesion, migration, and signaling, though its precise biological functions remain under investigation. Research highlights its potential role in cancer progression, particularly in metastasis and drug resistance. For instance, FNDC3B overexpression has been linked to enhanced invasiveness in hepatocellular carcinoma and breast cancer, possibly through interactions with signaling pathways like TGF-β or via modulation of extracellular matrix dynamics. Additionally, FNDC3B may regulate protein stability through partnerships with deubiquitinating enzymes such as USP15. Antibodies against FNDC3B are essential tools for detecting its expression patterns in tissues or cell lines via techniques like Western blotting, immunohistochemistry, or immunofluorescence. These antibodies aid in studying its subcellular localization, post-translational modifications, and interactions with binding partners. Emerging evidence also suggests FNDC3B involvement in non-cancer contexts, including neural development and lipid metabolism, broadening its research relevance. Commercial FNDC3B antibodies are typically validated for specificity using knockout controls or siRNA-mediated silencing. Despite progress, further studies are needed to fully elucidate its molecular mechanisms and therapeutic potential.

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