首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >QUANTITATION OF POLYMERASE CHAIN REACTION-AMPLIFIED DNA FRAGMENTS BY CAPILLARY ELECTROPHORESIS AND LASER-INDUCED FLUORESCENCE DETECTION
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QUANTITATION OF POLYMERASE CHAIN REACTION-AMPLIFIED DNA FRAGMENTS BY CAPILLARY ELECTROPHORESIS AND LASER-INDUCED FLUORESCENCE DETECTION

机译:毛细管电泳和激光诱导荧光定量定量聚合酶链反应扩增的DNA片段

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Quantitation of DNA fragments amplified by polymerase chain reaction (PCR) is needed for the determination of target DNA in molecular biology. Capillary electrophoresis in entangled polymer solution coupled to laser-induced fluorescence detection was assessed as an alternative technique to conventional slab gel methods to monitor competitive PCR, which consists of amplifying an internal standard fragment under the same conditions as the target fragment. The fluorescence signal was generated either through end-labeling of the fragments using 5'-fluorescein-labeled primers or through intercalation of ethidium bromide along the double strand. It is shown that the more accurate and reliable results were obtained using this latter pathway. [References: 20]
机译:需要定量通过聚合酶链反应(PCR)扩增的DNA片段,才能确定分子生物学中的目标DNA。缠结的聚合物溶液中的毛细管电泳与激光诱导的荧光检测相结合,被评估为监测竞争性PCR的常规平板凝胶法的替代技术,该方法包括在与靶标片段相同的条件下扩增内标片段。荧光信号是通过使用5'-荧光素标记的引物对片段进行末端标记或通过沿双链插入溴化乙锭生成的。结果表明,使用后一种途径可获得更准确和可靠的结果。 [参考:20]

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