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Single-Strand Conformation Polymorphism Analysis by Microchip Electrophoresis for the Rapid Detection of Point Mutation in Human Obesity Gene

机译:利用微芯片电泳分析单链构象多态性以快速检测人类肥胖基因中的点突变

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摘要

We describe an effective method of microchip electrophoresis(ME)based on single strand conformation polymorphism(SSCP)analysis to rapidly detect the point mutation,Leu72Met,in a human obesity gene.The 207-bp dsDNA in the Leu72Met region,an estimate of the child obesity DNA mutant,was amplified by polymerase chain reaction(PCR)and submitted to a conventional glass microchip analysis with a sieving matrix of 1.75% poly(vinylpyrrolidone)(M_r 1 300 000),1.0% poly(ethyleneoxide)(M_r 600 000)and 5.0% w/w glycerol.When combined with base stacking(BS)with hydroxide ions,the SSCP-ME provided rapid analysis as well as sensitive detection.The detection sensitivity was effectively enhanced in the OH~-concentration range of 0.01-0.025 M NaOH.The sensitivity and speed of this ME-based SSCP methodology for the rapid detection of Leu72Met point mutations makes this an attractive method for diagnosing childhood obesity in a clinical diagnostic laboratory.
机译:我们描述了一种基于单链构象多态性(SSCP)分析的微芯片电泳(ME)的有效方法,可以快速检测人类肥胖基因中的点突变Leu72Met.Leu72Met区的207-bp dsDNA估计儿童肥胖DNA突变体,通过聚合酶链反应(PCR)进行扩增,并以1.75%聚(乙烯基吡咯烷酮)(M_r 1 300 000),1.0%聚(环氧乙烷)(M_r 600 000 )和5.0%w / w甘油。与氢氧根离子的碱性堆积(BS)结合使用时,SSCP-ME提供了快速分析和灵敏检测的功能。在0.01〜的OH〜浓度范围内,检测灵敏度得到了有效提高。 0.025 M NaOH。这种基于ME的SSCP方法快速检测Leu72Met点突变的灵敏度和速度使其成为在临床诊断实验室中诊断儿童肥胖的诱人方法。

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