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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >RAPID AND ENHANCED DETECTION OF MITOCHONDRIAL DNA VARIATION USING SINGLE-STRAND CONFORMATION ANALYSIS OF SUPERPOSED RESTRICTION ENZYME FRAGMENTS FROM POLYMERASE CHAIN REACTION AMPLIFIED PRODUCTS
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RAPID AND ENHANCED DETECTION OF MITOCHONDRIAL DNA VARIATION USING SINGLE-STRAND CONFORMATION ANALYSIS OF SUPERPOSED RESTRICTION ENZYME FRAGMENTS FROM POLYMERASE CHAIN REACTION AMPLIFIED PRODUCTS

机译:利用聚合酶链反应扩增产物中的限制性酶切片段的单链构象快速检测和增强线粒体DNA变异

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摘要

A strategy is described for detecting mitochondrial (mt) DNA variation which permits rapid and straightforward screening for forensic purposes. The method is based on the selection of fragments with adequate length for performing single strand conformation polymorphism (SSCP) analysis selecting a set of restriction enzymes (RE) which yield fragments with prefixed lengths. After digestion of mtDNA by the appropriate enzyme or set of enzymes, SSCP analysis is performed in a semiautomatic electrophoretic system using a silver staining detection method. The conformational changes due to single mutations were therefore found not to change the electrophoretic protocol but to change the relative position of the mutations within the fragment. The discrimination power of this method is estimated to be 90% when two restriction enzymes (MspI and Hinfl) are used, but it is considerably higher when other enzymes are added. [References: 15]
机译:描述了一种检测线粒体(mt)DNA变异的策略,该策略可快速简便地筛查法医。该方法基于选择具有足够长度的片段以进行单链构象多态性(SSCP)分析,并选择一组限制性酶(RE),这些限制性酶可产生具有前缀长度的片段。用适当的一种或多种酶消化mtDNA后,使用银染检测方法在半自动电泳系统中进行SSCP分析。因此发现由于单个突变而引起的构象变化不会改变电泳方案,而是会改变片段内突变的相对位置。当使用两种限制性内切酶(MspI和Hinf1)时,该方法的鉴别力估计为90%,但是当添加其他酶时,其鉴别力则更高。 [参考:15]

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