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DNA Amplification Efficiencies of PCR Chips Using Different Heaters and Channels

机译:使用不同加热器和通道的PCR芯片的DNA扩增效率

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This paper presents the effect of temperature distributions in different heaters and channels on DNA amplification for polymerase chain reaction biochip. We utilized the Micro-Electro-Mechanical System to complete biochip accuracy. The TPX (Poly-4-methyl-pentene-1) was used as the polymer material. The microchip composed of two parts. One is the heater and temperature sensor on a top cover, the other is the microchannel and reaction chamber on a bottom substrate. Then we designed two kinds of chip materials : 1. a glass cover and a TPX substrate, 2. a TPX cover and a TPX substrate. Temperature is the most important in PCR, so the more uniform one is better. And we designed two kinds of heater. According to heat conduction simulation, we can find the best heater pattern. The simulation result is that the design of long inside distance and short outside distance between heater columns was the best one. The reagent of 10 μL was repeated twenty-five cycles to complete PCR process. The temperature controller could reach the speed of heating 20 ℃ /sec and the speed of cooling 5℃ /sec. Thus the PCR process could be achieved for twenty-five cycles within 35 minutes. Finally we used the instruments to check DNA amplification result qualitatively and quantitatively. The DNA amplification length was 108 bps. The DNA amplification of long inside distance and short outside distance between heater columns was 90.17 ng/μL, and was larger 12 ng/μL than that of equally distances. Excellent correlation between simulation analysis and experimental result was obtained in this study.
机译:本文介绍了不同加热器和通道的温度分布对聚合酶链反应生物芯片DNA扩增的影响。我们利用微机电系统来完善生物芯片的准确性。 TPX(Poly-4-methyl-pentene-1)用作聚合物材料。微芯片由两部分组成。一个是位于顶盖上的加热器和温度传感器,另一个是位于底部基板上的微通道和反应室。然后,我们设计了两种芯片材料:1.玻璃盖和TPX基板; 2. TPX盖和TPX基板。温度在PCR中最重要,因此温度越均匀越好。并且我们设计了两种加热器。根据热传导模拟,我们可以找到最佳的加热器模式。仿真结果表明,加热柱之间的内距离长,外距离短是最好的设计。将10μL试剂重复25个循环以完成PCR过程。温度控制器可以达到20℃/ sec的加热速度和5℃/ sec的冷却速度。因此,可以在35分钟内完成25个循环的PCR过程。最后,我们使用仪器对DNA扩增结果进行了定性和定量检查。 DNA扩增长度为108bps。加热柱之间的长内部距离和短外部距离的DNA扩增为90.17 ng /μL,比等距离的DNA扩增大12 ng /μL。在这项研究中获得了仿真分析和实验结果之间的极好的相关性。

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