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ASSESSMENT OF COMPUTERIZED AND MANUAL ANALYSIS OF SLIDES PROCESSED IN SINGLE CELL GEL ELECTROPHORESIS ASSAY

机译:单细胞凝胶电泳分析过程中滑板的计算机化评估和人工分析

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摘要

The comet assay, also called the single-cell gel elec-trophoresis (SCGE) assay, is a rapid, simple and sensitive microgel electrophoresis technique for measuring DNA damages (strand breaks and alkali-labile sites) in individual cells. The technique enables us to evaluate the mechanisms of genotoxic and cytotoxic effects of physical and chemical agents on living organisms. In principal, isolated DNA from cells are embedded in agarose, was unwound in an alkaline buffer, and is subjected to a weak electric current in which the broken negatively charged DNA becomes free to move towards the anode. The migrated DNA structures stained with a fluorescent dye resemble a shape of a "comet" when observed by fluorescence microscopy. The intensity of the comet tail relative to the head reflects the number of DNA breaks. The analysis of comets is generally carried out with either the use of a computer image-analysis program or with manual scoring through a scale. There are several image analysis programs commercially available providing a large number of measurement outcomes (i.e., tail length, tail moment, etc.) to evaluate the extent of DNA damage. However, these are highly expensive methods and need to be updated on a regular basis. In this study, we compared analysis of the same slides by CASP~? (comet analysis software program) and a manual method. The manual method for comet analysis provided good and reliable data and correlated well with the parameters, such as TM (tail moment), OTM (Olive tail moment), comet length etc., obtained from the CASP~?. However, the analysis of comets with CASP~? minimized time, faults and expertise but offered a large number of comets to be analyzed with many valuable parameters. The image analysis program is freely available and meets the necessity of parameters of many commercially available programs.
机译:彗星测定法,也称为单细胞凝胶电泳(SCGE)测定法,是一种快速,简单且灵敏的微凝胶电泳技术,用于测量单个细胞中的DNA损伤(链断裂和碱不稳定位点)。该技术使我们能够评估物理和化学试剂对生物体的遗传毒性和细胞毒性作用的机制。原则上,从细胞中分离出的DNA被嵌入琼脂糖中,在碱性缓冲液中解开,并受到弱电流的作用,其中破碎的带负电荷的DNA可以自由地向阳极移动。当通过荧光显微镜观察时,被荧光染料染色的迁移的DNA结构类似于“彗星”的形状。彗尾相对于头部的强度反映了DNA断裂的次数。彗星的分析通常通过使用计算机图像分析程序或通过刻度进行手动评分来进行。商业上有几种图像分析程序可提供大量的测量结果(即尾长,尾矩等)来评估DNA损伤的程度。但是,这些都是非常昂贵的方法,需要定期进行更新。在这项研究中,我们比较了CASP〜?对相同幻灯片的分析。 (彗星分析软件程序)和手动方法。手工进行彗星分析的方法提供了良好而可靠的数据,并且与从CASP〜?获得的参数(如TM(尾矩),OTM(橄榄尾矩),彗星长度等)相关性很好。但是,用CASP分析彗星〜?最大限度地减少了时间,故障和专业知识,但提供了许多具有许多有价值参数的待分析彗星。图像分析程序是免费提供的,并且满足许多市售程序的参数要求。

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