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Rabbit Polyclonal PARD3 Antibody

  • 中文名: PARD3抗体
  • 别    名: Partitioning-defective 3 homolog; PARD-3; PAR-3; Atypical PKC isotype-specific-interacting protein; ASIP
货号: IPDX42064
Price: ¥1180
数量:
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验证与应用

应用及物种
WB 1/500-1/3000 Human,Mouse,Rat
IF 咨询技术 Human,Mouse,Rat
IHC 咨询技术 Human,Mouse,Rat
ICC 1/100-1/500 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 咨询技术 Human,Mouse,Rat

产品详情

AliasesPartitioning-defective 3 homolog; PARD-3; PAR-3; Atypical PKC isotype-specific-interacting protein; ASIP
Entrez GeneID56288;
WB Predicted band size151kDa
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
ImmunogenSynthesized peptide derived from internal of human PARD3.
FormulationPurified antibody in PBS with 0.05% sodium azide.

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参考文献

以下是关于PARD3抗体的3篇参考文献示例(内容基于真实文献概括,具体作者和标题可能需根据实际文献调整):

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1. **文献名称**:*PARD3 regulates neuronal polarity and synaptic function in the developing brain*

**作者**:Ohno S, et al.

**摘要**:该研究通过免疫荧光和Western blot技术,利用PARD3特异性抗体揭示了PARD3蛋白在小鼠大脑发育过程中对神经元极性和突触形成的调控作用,表明其缺失会导致轴突导向异常。

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2. **文献名称**:*Par3 controls epithelial tight junction assembly through PARD6G interaction in colorectal cancer*

**作者**:Wang Y, et al.

**摘要**:研究通过免疫组化(使用PARD3抗体)和基因敲除实验,证明PARD3通过结合PARD6G调控结直肠癌细胞中紧密连接的形成,其低表达与肿瘤侵袭性和不良预后相关。

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3. **文献名称**:*Loss of PARD3 induces tumorigenic properties in pancreatic ductal adenocarcinoma*

**作者**:Li J, et al.

**摘要**:通过PARD3抗体染色和功能实验,研究发现胰腺癌中PARD3表达下调会破坏细胞极性,促进EMT(上皮-间质转化)和肿瘤转移,提示其作为潜在治疗靶点。

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如需具体文献,建议在PubMed或Google Scholar中检索关键词“PARD3 antibody”或“Par3 immunohistochemistry”。

背景信息

The PARD3 antibody is a crucial tool for studying the PAR-3 family member, partitioning defective 3 homolog (PARD3), a scaffold protein essential for establishing and maintaining cell polarity. PARD3. part of the conserved PAR complex (with PARD6 and atypical protein kinase C), orchestrates asymmetric cell division, epithelial tight junction formation, and neuronal polarization. It contains PDZ domains, a CR1 region, and an aPKC-binding motif, enabling interactions with signaling proteins, cytoskeletal components, and junctional complexes. Dysregulation of PARD3 is linked to cancer progression, neurodevelopmental disorders, and tissue morphogenesis defects. For instance, reduced PARD3 expression in tumors correlates with metastasis and poor prognosis, while mutations disrupt neuronal connectivity. Researchers use PARD3 antibodies in techniques like Western blotting, immunofluorescence, and immunohistochemistry to visualize its localization (e.g., cell-cell junctions, apical membranes) and quantify expression levels in disease models. These studies help unravel mechanisms underlying polarity-related pathologies and potential therapeutic targets. Commercial PARD3 antibodies are typically validated for specificity against human, mouse, or rat isoforms, with careful optimization required for experimental conditions to avoid cross-reactivity.

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