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Real-Time Polymerase Chain Reaction as a Tool for Evaluation of Magnetic Poly(Glycidyl methacrylate)-Based Microspheres in Molecular Diagnostics

机译:实时聚合酶链反应作为评估基于磁性聚甲基丙烯酸缩水甘油酯的微球在分子诊断中的工具

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摘要

DNA amplification by real-time polymerase chain reaction (RT-PCR) was used for the evaluation of efficiency of polymer coating of magnetic hydrophilic poly(2-hydroxyethyl methacrylate-co-glycidyl methacrylate) (P(HEMA-co-GMA)) and poly(glycidyl methacrylate) (PGMA) microspheres with/without carboxyl groups. The inhibition effect of magnetic microspheres on real-time polymerase chain reaction (RT-PCR) course was evaluated by regression analysis after the addition of different concentrations of tested microspheres to PCR mixtures. Microspheres mostly did not interfere in RT-PCR till the concentration 50 mu g/25 mu l PCR mixture. No relationship between Fe content (and microsphere diameter) and inhibition effect was found. Microspheres containing carboxyl groups extinguished the fluorescence at lower concentrations (10-20 mu g/25 mu l PCR mixture) without inhibition of DNA amplification as PCR products were detected using agarose gel electrophoresis. Negative effect of maghemite on PCR course was partially reduced by coating of magnetic core by silica or polymers. Two inhibition mechanisms of DNA amplification were discussed in this work.
机译:通过实时聚合酶链反应(RT-PCR)进行的DNA扩增用于评估磁性亲水性聚甲基丙烯酸2-羟乙酯-甲基丙烯酸缩水甘油酯(P(HEMA-co-GMA))和具有/不具有羧基的聚(甲基丙烯酸缩水甘油酯)(PGMA)微球。在向PCR混合物中添加不同浓度的测试微球后,通过回归分析评估了磁性微球对实时聚合酶链反应(RT-PCR)过程的抑制作用。直到浓度为50μg/ 25μlPCR混合物时,微球大部分才对RT-PCR产生干扰。铁含量(和微球直径)与抑制作用之间没有关系。含有羧基的微球在较低浓度(10-20μg/ 25μlPCR混合物)下可消除荧光,而不会抑制DNA扩增,因为使用琼脂糖凝胶电泳检测到PCR产物。磁赤铁矿对PCR进程的负面影响通过用二氧化硅或聚合物包覆磁芯而部分降低。在这项工作中讨论了DNA扩增的两种抑制机制。

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