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Biomicrofluidics. 2010 Sep 30;4(3):32209. doi: 10.1063/1.3463720.
2
Amplification of SPPS150 and Salmonella typhi DNA with a high throughput oscillating flow polymerase chain reaction device.高通量振荡流聚合酶链反应装置扩增 SPPS150 和伤寒沙门氏菌 DNA。
Biomicrofluidics. 2010 May 3;4(2):024103. doi: 10.1063/1.3422524.
3
A Continuous-Flow Polymerase Chain Reaction Microchip With Regional Velocity Control.一种具有区域速度控制的连续流动聚合酶链反应微芯片。
J Microelectromech Syst. 2006 Feb 1;15(1):223-236. doi: 10.1109/JMEMS.2005.859083.
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Polydimethylsiloxane microfluidic chip with integrated microheater and thermal sensor.聚二甲基硅氧烷微流控芯片,集成微加热器和热敏传感器。
Biomicrofluidics. 2009 Jan 2;3(1):12005. doi: 10.1063/1.3058587.
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Design and integration of an all-in-one biomicrofluidic chip.一体式生物微流控芯片的设计与集成。
Biomicrofluidics. 2008 Jul 21;2(3):34103. doi: 10.1063/1.2966453.
6
Amplification of ST50 gene using dry-reagent-based polymerase chain reaction for the detection of Salmonella typhi.使用基于干试剂的聚合酶链反应扩增ST50基因以检测伤寒沙门氏菌。
Diagn Microbiol Infect Dis. 2007 Dec;59(4):373-7. doi: 10.1016/j.diagmicrobio.2007.05.014. Epub 2007 Oct 25.
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Self-actuated, thermo-responsive hydrogel valves for lab on a chip.用于芯片实验室的自驱动热响应水凝胶阀
Biomed Microdevices. 2005 Dec;7(4):313-22. doi: 10.1007/s10544-005-6073-z.
8
Micro flow-through PCR in a PMMA chip fabricated by KrF excimer laser.在由KrF准分子激光制造的聚甲基丙烯酸甲酯芯片中进行微流通式聚合酶链式反应。
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9
Ligase detection reaction/hybridization assays using three-dimensional microfluidic networks for the detection of low-abundant DNA point mutations.使用三维微流控网络进行连接酶检测反应/杂交分析以检测低丰度DNA点突变
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Microchip PCR.微芯片聚合酶链反应
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利用旋转线性聚合酶链反应装置(PCRDisc)快速多重样本 DNA 扩增。

Rapid multi sample DNA amplification using rotary-linear polymerase chain reaction device (PCRDisc).

出版信息

Biomicrofluidics. 2012 Mar;6(1):14119-1411913. doi: 10.1063/1.3690469. Epub 2012 Mar 14.

DOI:10.1063/1.3690469
PMID:22685508
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3370399/
Abstract

Multiple sample DNA amplification was done by using a novel rotary-linear motion polymerase chain reaction (PCR) device. A simple compact disc was used to create the stationary sample chambers which are individually temperature controlled. The PCR was performed by shuttling the samples to different temperature zones by using a combined rotary-linear movement of the disc. The device was successfully used to amplify up to 12 samples in less than 30 min with a sample volume of 5 μl. A simple spring loaded heater mechanism was introduced to enable good thermal contact between the samples and the heaters. Each of the heater temperatures are controlled by using a simple proportional-integral-derivative pulse width modulation control system. The results show a good improvement in the amplification rate and duration of the samples. The reagent volume used was reduced to nearly 25% of that used in conventional method.

摘要

采用新型旋转-直线运动聚合酶链反应(PCR)装置进行了多个样本 DNA 扩增。使用简单的光盘创建了单独控温的固定样本室。通过使用光盘的组合旋转-直线运动将样品移动到不同的温度区域来进行 PCR。该装置成功地在不到 30 分钟的时间内使用 5μl 的样品体积扩增了多达 12 个样本。引入了简单的弹簧加载加热机制,以实现样品和加热器之间的良好热接触。每个加热器温度都通过使用简单的比例积分微分脉冲宽度调制控制系统进行控制。结果表明,样品的扩增速率和持续时间有了很好的提高。所用试剂的体积减少到传统方法的近 25%。