首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Development of micropump-actuated negative pressure pinched injection for parallel electrophoresis on array microfluidic chip.
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Development of micropump-actuated negative pressure pinched injection for parallel electrophoresis on array microfluidic chip.

机译:用于阵列微流控芯片上平行电泳的微型泵致动负压夹紧式注射的开发。

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摘要

A micropump-actuated negative pressure pinched injection method is developed for parallel electrophoresis on a multi-channel LIF detection system. The system has a home-made device that could individually control 16-port solenoid valves and a high-voltage power supply. The laser beam is excitated and distributes to the array separation channels for detection. The hybrid Glass-PDMS microfluidic chip comprises two common reservoirs, four separation channels coupled to their respective pneumatic micropumps and two reference channels. Due to use of pressure as a driving force, the proposed method has no sample bias effect for separation. There is only one high-voltage supply needed for separation without relying on the number of channels, which is significant for high-throughput analysis, and the time for sample loading is shortened to 1 s. In addition, the integrated micropumps can provide the versatile interface for coupling with other function units to satisfy the complicated demands. The performance is verified by separation of DNA marker and Hepatitis B virus DNA samples. And this method is also expected to show the potential throughput for the DNA analysis in the field of disease diagnosis.
机译:针对多通道LIF检测系统上的平行电泳,开发了一种微泵驱动的负压夹压进样方法。该系统具有一个可以单独控制16通电磁阀和高压电源的自制设备。激光束被激发并分布到阵列分离通道以进行检测。混合型Glass-PDMS微流体芯片包括两个公共储液器,四个与各自的气动微型泵相连的分离通道和两个参考通道。由于使用压力作为驱动力,所以所提出的方法没有分离样品的偏见效应。仅需一个高压电源即可进行分离,而无需依赖通道数,这对于高通量分析非常重要,并且样品加载时间缩短到1 s。此外,集成的微型泵可以提供用于与其他功能单元耦合的通用接口,以满足复杂的需求。通过分离DNA标记物和乙型肝炎病毒DNA样品验证了性能。并且该方法也有望显示出在疾病诊断领域进行DNA分析的潜在通量。

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