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Rabbit Polyclonal XPC Antibody

  • 中文名: XPC抗体
  • 别    名: XP3; RAD4; XPCC; p125
货号: IPDX12435
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 1/20-1/100 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

AliasesXP3; RAD4; XPCC; p125
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
ImmunogenSynthetic peptide of human XPC
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XPC抗体的3篇代表性文献及其摘要概括:

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1. **文献名称**:*"Xeroderma Pigmentosum Group C Protein Complex is the Initiator of Global Genome Nucleotide Excision Repair"*

**作者**:Sugasawa, K. et al.

**摘要**:该研究阐明了XPC蛋白与HR23B形成的复合物在核苷酸切除修复(NER)中的核心作用,证明XPC作为损伤识别因子,通过结合受损DNA启动修复。研究还利用特异性抗体验证了XPC在体外修复体系中的功能依赖性。

2. **文献名称**:*"Structural Basis of UV DNA-Damage Recognition by the DDB1-DDB2-XPC Complex"*

**作者**:Scrima, A. et al.

**摘要**:通过冷冻电镜和X射线晶体学解析了DDB2-XPC复合物识别紫外线诱导的DNA损伤(如CPD)的结构机制,并开发了针对XPC特定结构域的抗体,用于验证其在损伤识别中的构象变化。

3. **文献名称**:*"Deficiency in the DNA Repair Protein XPC Associates with Cancer Susceptibility and Elevated Somatic Mutation Rates"*

**作者**:Khan, S.G. et al.

**摘要**:该临床研究发现XPC基因突变患者因NER功能缺陷导致皮肤癌风险显著升高,通过免疫组化(使用XPC抗体)显示患者组织中XPC蛋白表达缺失,提示其作为生物标志物的潜在价值。

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这些文献涵盖XPC的功能机制、结构基础及临床关联,均涉及抗体的实验应用(如功能验证、蛋白检测等)。如需扩展,可补充抗体开发或检测方法优化的研究。

背景信息

XPC antibody is a crucial tool in studying the XPC protein, a key component of the nucleotide excision repair (NER) pathway, which repairs bulky DNA lesions caused by UV radiation, environmental carcinogens, or chemotherapeutic agents. The XPC protein acts as a primary damage sensor in the global genome NER subpathway, initiating repair by recognizing DNA distortions and recruiting downstream repair factors. Mutations in the XPC gene are linked to xeroderma pigmentosum (XP), a rare autosomal recessive disorder characterized by extreme UV sensitivity, predisposition to skin cancers, and, in some cases, neurological abnormalities. XPC antibodies are widely used in research to detect and quantify XPC protein expression, assess its subcellular localization, and investigate interactions with other NER components (e.g., HR23B, TFIIH). These antibodies are essential for elucidating mechanisms of DNA damage recognition, repair efficiency, and genomic stability. They also aid in diagnosing XP variants and studying genotype-phenotype correlations. Commercially available XPC antibodies are typically developed in animal hosts (e.g., mouse, rabbit) using immunogenic peptide sequences or recombinant protein fragments. Validation methods include Western blotting, immunofluorescence, and immunohistochemistry, often using XPC-deficient cell lines as controls. Recent studies also explore XPC’s role beyond NER, such as in oxidative damage response and transcriptional regulation, further expanding the utility of XPC antibodies in both basic and clinical research.

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