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Rabbit Polyclonal SDC2 Antibody

  • 中文名: SDC2抗体
  • 别    名: SYND2; Fibroglycan; Heparan sulfate proteoglycan core protein; HSPG;
货号: IPDX42628
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

AliasesSYND2; Fibroglycan; Heparan sulfate proteoglycan core protein; HSPG;
Entrez GeneID6383;
WB Predicted band size22kDa
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 SDC2.
FormulationPurified antibody in PBS with 0.05% sodium azide.

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参考文献

以下是3篇与SDC2抗体相关的代表性文献(内容为模拟概括,仅供参考):

1. **《Syndecan-2 (SDC2) as a Novel Biomarker in Colorectal Cancer Immunohistochemistry》**

- 作者:Kim et al. (2020)

- 摘要:研究验证了SDC2抗体在结直肠癌组织中的高特异性表达,证实其可作为早期癌症筛查的潜在生物标志物,并探讨了其与肿瘤侵袭性的关联。

2. **《Targeting SDC2 with a Monoclonal Antibody Inhibits Tumor Angiogenesis in Triple-Negative Breast Cancer》**

- 作者:Zhang et al. (2019)

- 摘要:开发了一种靶向SDC2的单克隆抗体,通过阻断SDC2与VEGF的相互作用抑制三阴性乳腺癌血管生成,动物实验显示显著降低肿瘤生长。

3. **《The Role of Anti-SDC2 Autoantibodies in Inflammatory Bowel Disease Pathogenesis》**

- 作者:Müller et al. (2021)

- 摘要:发现炎症性肠病(IBD)患者血清中SDC2自身抗体水平升高,提示SDC2可能参与肠道屏障破坏和炎症反应调控。

注:实际文献需通过PubMed/Google Scholar等平台检索确认。

背景信息

Syndecan-2 (SDC2), a member of the syndecan family of transmembrane heparan sulfate proteoglycans, plays critical roles in cell-matrix interactions, cell adhesion, migration, and intracellular signaling. It consists of an extracellular domain modified with glycosaminoglycan chains, a single transmembrane domain, and a cytoplasmic tail that interacts with cytoskeletal and signaling molecules. SDC2 is broadly expressed in various tissues, including endothelial cells, fibroblasts, and certain epithelial cells, and is involved in regulating processes such as angiogenesis, wound healing, and immune responses. Dysregulation of SDC2 has been implicated in pathological conditions, particularly cancer, where it may act as either a tumor suppressor or promoter depending on context. For example, SDC2 downregulation is linked to colorectal cancer progression, while its overexpression correlates with poor prognosis in breast and lung cancers. SDC2 antibodies are essential tools for studying its expression, localization, and function. They are widely used in techniques like immunohistochemistry, flow cytometry, and Western blotting to explore SDC2's role in disease mechanisms, tissue development, and potential therapeutic targeting. Recent research also investigates SDC2's interaction with extracellular matrix components and growth factors (e.g., FGF2. VEGF), highlighting its importance in cellular communication pathways.

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