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A new gravity-driven microfluidic-based electrochemical assay coupled to magnetic beads for nucleic acid detection

机译:一种新的重力驱动的基于微流体的电化学检测方法,结合磁珠进行核酸检测

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摘要

In this work, the characterisation and the optimisation of hybridisation assays based on a novel, rapid and sensitive micro-analytical, gravity-driven, flow device is reported. This device combines a special chip containing eight polymer microchannels, with a portable, computer-controlled instrument. The device is used as a platform for affinity experiments using oligonucleotide-modified paramagnetic particles. In our approach, both hybridisation and labelling events are performed on streptavidin-coated paramagnetic microparticles functionalised with a biotinylated capture probe. Modified particles, introduced in the microchannel inlet of the chip, accumulate near the electrode surface by virtue of a magnetic holder. After hybridisation with the complementary sequence, the hybrid is labelled with an alkaline phosphatase conjugate. The electrochemical substrate for alkaline phosphatase revelation is p-aminophenyl phosphate. Solutions and reagents are sequentially passed through the microchannels, until enzyme substrate is added for in situ signal detection. Upon readout, the magnet array is flipped away, beads are removed by addition of regeneration buffer, and the so-regenerated chip is ready for further analysis. This protocol has been applied to the analytical detection of specific DNA sequences of Legionella pneumophila, with an RSD=8.5% and a detection limit of 0.33 nM.
机译:在这项工作中,报告了基于新型,快速和灵敏的微分析,重力驱动的流动装置的杂交测定的表征和优化。该设备将包含八个聚合物微通道的特殊芯片与便携式计算机控制仪器结合在一起。该设备用作使用寡核苷酸修饰的顺磁性颗粒进行亲和实验的平台。在我们的方法中,杂交和标记事件均在用生物素化捕获探针功能化的链霉亲和素包被的顺磁性微粒上进行。引入芯片的微通道入口中的改性颗粒借助磁性支架聚集在电极表面附近。与互补序列杂交后,用碱性磷酸酶缀合物标记杂合体。碱性磷酸酶揭露的电化学底物是对氨基苯基磷酸酯。溶液和试剂依次通过微通道,直到添加酶底物用于原位信号检测。读出后,将磁铁阵列翻转开,通过添加再生缓冲液去除磁珠,这样再生的芯片即可用于进一步分析。该方案已用于肺炎军团菌特定DNA序列的分析检测,RSD = 8.5%,检出限为0.33 nM。

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