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AN ELECTROKINETICALLY CONTROLLED DNA HYBRIDIZATION CHIP

机译:电动控制的DNA杂交芯片

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Biosensors and more specifically biochips exploit the interactions between a target analyte and an immobilized biological recognition element to produce a measurable signal. Systems based on surface phase nucleic acid hybridization, such as modern microarrays, are particularly attractive due to the high degree of selectivity in the binding interactions. One drawback of this reaction is the relatively long time required for complete hybridization to occur, as a result of the diffusion limited reaction kinetics. In this work an electrokinetically controlled DNA hybridization microfluidic chip will be introduced. The electrokinetic delivery technique provides the ability to dispense controlled sample sizes to the hybridization array while serving to increase the mass transfer rate and therefore the reaction speed. The focus of this paper will be on the design and microfabrication of the chip, the unique H-type channel structure and electrokinetic sample delivery and washing technique, and development of the on-line hybridization scanning. Initial hybridization results presented here demonstrate that less than 5 minutes and 4.9nL of 0.5μM ssDNA sample was required (35s dispensing period followed by a 4 minute wash) for complete hybridization.
机译:生物传感器和更具体地说,Biochips利用靶分析物和固定化的生物学识别元件之间的相互作用来产生可测量的信号。基于表面相核酸杂交的系统,例如现代微阵列,由于结合相互作用的高度选择性,是特别有吸引力。这种反应的一个缺点是由于扩散有限的反应动力学而发生完全杂交所需的相对长的时间。在这项工作中,将引入电动控制的DNA杂交微流体芯片。电动递送技术提供将控制样本尺寸分配给杂交阵列的能力,同时用于增加质量传递速率并因此增加反应速度。本文的焦点将在芯片的设计和微制造上,独特的H型通道结构和电动样品递送和洗涤技术,以及开发在线杂交扫描。本文介绍的初始杂交结果表明,需要小于5分钟和4.9NL的0.5μmSSDNA样品(35s分配时,其次洗涤4分钟后),以完全杂交。

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