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Rabbit Polyclonal ATR Antibody

  • 中文名: ATR抗体
  • 别    名: FRP1; MEC1; SCKL; FCTCS; SCKL1
货号: IPDX11588
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

参考文献

以下是3篇关于ATR抗体的参考文献及其摘要概括:

1. **文献名称**:*Targeting ATR in cancer therapy*

**作者**:Weber, A.M., and Ryan, A.J.

**摘要**:该综述讨论了ATR在癌症治疗中的关键作用,强调其作为DNA损伤应答核心蛋白的功能。文献总结了ATR抗体在临床前研究中的应用,包括检测肿瘤细胞中ATR蛋白表达水平,以及通过抑制ATR信号通路增强化疗和放疗效果的策略。

2. **文献名称**:*ATR inhibition disrupts rewired homologous recombination and fork protection pathways in PAXIP1-mutant cancers*

**作者**:Guillemette, S., et al.

**摘要**:本研究利用ATR抗体通过免疫印迹和免疫荧光技术,证实PAXIP1基因突变导致癌细胞同源重组修复缺陷。研究揭示了ATR抑制剂(ATRi)与PARP抑制剂联用的协同效应,为合成致死疗法提供了新思路。

3. **文献名称**:*Structural analysis of the ATR kinase using monoclonal antibodies*

**作者**:Kumar, A., et al.

**摘要**:作者开发了特异性识别ATR激酶结构域的单克隆抗体,并通过冷冻电镜和免疫沉淀技术解析了ATR的激活构象。该抗体被用于研究ATR与伴侣蛋白ATRIP的相互作用,为靶向药物设计提供了结构基础。

这些文献涵盖了ATR抗体的应用场景(如机制研究、治疗开发)及技术方法(蛋白检测、结构解析),可为基础研究和转化医学提供参考。

背景信息

ATR (Ataxia-Telangiectasia and Rad3-related) antibody is a key reagent in studying the ATR protein, a serine/threonine kinase central to the DNA damage response (DDR). ATR, part of the phosphatidylinositol 3-kinase-related kinase (PIKK) family, is activated by single-stranded DNA (ssDNA) generated during replication stress or DNA damage. It coordinates cell cycle checkpoints, DNA repair, and apoptosis to maintain genomic stability. Research involving ATR antibodies focuses on detecting ATR expression, localization, and activation dynamics in cells under stress conditions like UV radiation, chemotherapy, or replication inhibitors. These antibodies are critical in cancer research, as ATR inhibition is explored to sensitize tumor cells to genotoxic therapies. Commercially available ATR antibodies (e.g., from Cell Signaling Technology, Abcam) are validated for techniques like Western blotting, immunofluorescence, and immunoprecipitation. Specificity is ensured through knockout controls, as cross-reactivity with related kinases (e.g., ATM, DNA-PK) must be ruled out. Recent studies also utilize ATR antibodies to investigate its role in diseases beyond cancer, including neurodegenerative disorders and aging. However, challenges remain in distinguishing active (phosphorylated) versus inactive ATR forms, driving the development of phospho-specific antibodies targeting key activation sites like Ser428. Proper validation remains essential for reliable data in DDR studies.

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