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Measurement of Enzyme Activity Using a Plug-based Electrochemical Microdevice

机译:使用塞式电化学微型微型测量酶活性

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Determination of the activity of an enzyme in a solution of nL order was conducted using an electrochemical device with a plug-based microfluidic processing function. β-galactosidase (β-Gal) and adenosine triphosphatase (ATPase) were used as analyte enzymes. β-Gal is often used to be conjugated with antibodies, whereas the latter plays critical roles in cell functions. The activity of the enzymes was determined by measuring the concentration of one of the final products, p-aminophenol (PAP) or hydrogen peroxide (H_2O_2) by coulometry. Preparation of plugs of solutions of predetermined volumes and mixing of solutions was carried out using a T-junction on the device. A partially shallow flow channel structure was designed in the sensing area to improve collection efficiency. The observed output charge was correlated well with the amount of PAP or H_2O_2, which served as an indicator of the enzyme activity.
机译:使用具有基于塞子的微流体处理功能的电化学装置进行N1级溶液中酶的活性。使用β-半乳糖苷酶(β-加仑)和腺苷三磷酸酶(ATP酶)作为分析物酶。 β-GAL通常用于与抗体缀合,而后者在细胞功能中起着关键作用。通过测量最终产物,对氨基苯酚(PAP)或通过库仑法的过氧化氢(H_2O_2)的浓度来确定酶的活性。使用该装置上的T型连接进行预定体积的溶液和溶液混合的溶液的制备。在传感区域中设计了部分浅的流动通道结构以提高收集效率。观察到的输出电荷与PAP或H_2O_2的量相关,其用作酶活性的指标。

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