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Polymerase Chain Reaction using V Shape Thermal Cycling Program

机译:使用 V形热循环程序的聚合酶链式反应

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摘要

Polymerase chain reaction (PCR) is the most commonly used technique in molecular biology and diagnostics. To achieve faster PCR reaction time, two strategies were employed by previous studies. That includes improving the thermal ramp rate by developing novel devices to reduce the time wasted on temperature transitions and cutting the holding time in every step, which could even lead to compromise in amplification efficiency. Hence the need to further improve the technique.>Methods: A different way to achieve fast DNA amplification is developed by using the previously thought wasted time spent on heating and cooling the samples to finish the amplification. That means the holding time of the three procedures are omitted and this could be carried out on the ordinary PCR thermal cyclers.>Results: 2/3 of the amplification time is easily saved, compared to the conventionally used method. Additionally, the reaction time could be further reduced by using longer primers with higher melting temperature (Tm). The record time of the “V” shape Polymerase chain reaction (VPCR) conducted on ordinary PCR machine for amplification of a 98 bp fragment is 8 min. Furthermore, VPCR still retains the merits of traditional PCR technique, including specificity, sensitivity, generality, and compatibility with quantitative detection.>Conclusion: It is confirmed that the three procedures of PCR could be completed during the dynamic heating and cooling process when the cyclers are run at a moderate thermal ramp rate. As VPCR described here is based on the current PCR system, it could be implemented in any biological Lab immediately and provide great convenience to the people working in the field of life science and human health.
机译:聚合酶链反应(PCR)是分子生物学和诊断学中最常用的技术。为了获得更快的PCR反应时间,先前的研究采用了两种策略。这包括通过开发新颖的设备来减少温度转换所浪费的时间,并减少每一步的保持时间,从而提高热升温速率,这甚至可能导致放大效率下降。因此,有必要进一步改进该技术。>方法:通过使用先前认为浪费的加热和冷却样品以完成扩增所花费的时间,开发了另一种实现快速DNA扩增的方法。这意味着可以省去这三个步骤的保留时间,而可以在普通的PCR热循环仪上进行。>结果:与传统方法相比,可以节省2/3的扩增时间。另外,通过使用具有较高熔融温度(Tm)的较长的引物可以进一步减少反应时间。在普通PCR仪上进行98 bp片段扩增的“ V”形聚合酶链反应(VPCR)的记录时间为8分钟。此外,VPCR仍然保留了传统PCR技术的优点,包括特异性,灵敏度,通用性和与定量检测的兼容性。>结论:证实了在动态加热过程中可以完成PCR的三个步骤。循环器以适当的热升温速率运行时的冷却和冷却过程。由于此处描述的VPCR基于当前的PCR系统,因此可以立即在任何生物实验室中实施,并为在生命科学和人类健康领域工作的人们提供了极大的便利。

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