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首页> 外文期刊>Nuclear Instruments & Methods in Physics Research. B, Beam Interactions with Materials and Atoms >Methods for quantitative evaluation of dynamics of repair proteins within irradiated cells
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Methods for quantitative evaluation of dynamics of repair proteins within irradiated cells

机译:定量评估照射细胞内修复蛋白动态的方法

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Living HeLa cells are irradiated well directed with single 100 MeV oxygen ions by the superconducting ion microprobe SNAKE, the Superconducting Nanoscope for Applied Nuclear (=Kern-) Physics Experiments, at the Munich 14 MV tandem accelerator. Various proteins, which are involved directly or indirectly in repair processes, accumulate as clusters (so called foci) at DNA-double strand breaks (DSBs) induced by the ions. The spatiotemporal dynamics of these foci built by the phosphorylated histone gamma-H12AX are studied. For this Purpose cells are irradiated in line patterns. The gamma-H2AX is made visible under the fluorescence microscope using immunofluorescence techniques. Quantitative analysis methods are developed to evaluate the data of the microscopic images in order to analyze movement of the foci and their changing size. (c) 2005 Elsevier B.V. All rights reserved.
机译:在慕尼黑14 MV串联加速器上,超导离子微探针SNAKE(用于应用核(=核)物理实验的超导纳米镜)以100 MeV的单个氧离子很好地指导了活HeLa细胞。直接或间接参与修复过程的各种蛋白质在离子诱导的DNA双链断裂(DSB)处聚集成簇(所谓的焦点)。研究了由磷酸化的组蛋白γ-H12AX建立的这些病灶的时空动力学。为此,以线状图案照射细胞。使用免疫荧光技术,可以在荧光显微镜下看到gamma-H2AX。开发了定量分析方法以评估显微图像的数据,以便分析病灶的运动及其变化的大小。 (c)2005 Elsevier B.V.保留所有权利。

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