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首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Direct quantification of mitochondrial DNA and its 4.9-kb common deletion without DNA purification
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Direct quantification of mitochondrial DNA and its 4.9-kb common deletion without DNA purification

机译:无需DNA纯化即可直接定量线粒体DNA及其4.9kb的常见缺失

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摘要

Quantitative analysis of mitochondrial DNA (mtDNA) and its common deletion (CD) are sensitive and early markers for mitochondrial mutations and suffering. However, the use of purified DNA can lead to quantification errors because of variable DNA extraction yields due to the significant differences in size and structure between genomic DNA (gDNA) and mtDNA. We report a real-time qPCR-based protocol directly on tissue lysate, without DNA extraction. This method, which allows both absolute and relative measure, increases the measuring accuracy of the mtDNA/gDNA ratio and leads to reliable and more reproducible results when measuring the deleted/total mtDNA ratio.
机译:线粒体DNA(mtDNA)及其常见缺失(CD)的定量分析是线粒体突变和痛苦的敏感和早期标记。但是,由于基因组DNA(gDNA)和mtDNA在大小和结构上存在显着差异,纯化的DNA的使用会导致定量提取错误,这是因为DNA提取量可变。我们直接在组织裂解液上报告基于实时qPCR的协议,而无需提取DNA。此方法允许绝对和相对测量,可提高mtDNA / gDNA比率的测量准确性,并在测量缺失的mtDNA /总mtDNA比率时可提供可靠且可重复的结果。

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