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- 详细信息
- 文献和实验
- 技术资料
- 库存:
100
- 供应商:
上海博湖
- 检测范围:
0.156-10ng/ml
- 检测方法:
Sandwich ELISA, Double Antibody
- 应用:
0.094ng/ml
- 样本:
ATM
- 规格:
96T
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文献和实验A Human Cell Extract-Based Assay for the Activation of ATM and ATR Checkpoint Kinases
assay to study the activation of ATM and ATR by double-stranded DNA breaks (DSBs) (Shiotani and Zou, 2009, Mol Cell 33 , 547–58). In this assay, DNA fragments with different structural features are used to activate ATM and ATR in human cell extracts
的原理用于分子诊断方面:TrimGen公司的KRAS Mutation Detection Kit在96孔板里一次能实现7/8个KRAS突变位点的检测。 另外基于相同原理的技术还有PPT-ELISA。这是用来筛截短突变的,相关文章见:1,Rapid screen for truncating ATM mutations by PTT-ELISA . 2,An ELISA-based high throughput protein truncation test
Detecting the Influence of Cell Cycle Regulatory Proteins on Human Telomeres
orchestrating the responses to DNA damage, influences telomere metabolism as well as the function of cell cycle regulatory proteins. In mitotic cells, ataxia telangiectasia mutant (ATM) is required for a DNA damage-dependent signal-transduction cascade
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