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CHANNEL ELECTROPHORESIS FOR KINETIC ASSAYS

机译:动力学测定的通道电泳

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A rectangular channel electrophoresis system and a cylindrical sampling capillary combination allows chemical changes in nanoliter-volume samples to be monitored as a function of time. The electrophoretic microseparation is carried out in a rectangular channel with a 7-cm-long, 40-mu m x 2.5-cm geometry and is coupled to a 50-mu m-i.d. cylindrical sample introduction capillary. The channel width dimension is used as a time axis by moving the outlet of the sampling capillary across the entrance of the separation channel. Detection of the separated analyte bands is achieved with laser-induced fluorescence and spatially resolved detection based on a charge-coupled device. The system is characterized with a series of fluorescein thiocarbamyl amino acid derivatives; limits of detection are < 10(-8) M for amino acids and 10(-9) M (425 zmol) for fluorescein. The ability to achieve a time-based dynamic microseparation is demonstrated by monitoring fluorescent product formation during the enzyme-catalyzed hydrolysis of fluorescein di-beta-D-galactopyranoside (FDG), a commonly used fluorescent substrate for enzymological studies.
机译:矩形通道电泳系统和圆柱形采样毛细管组合可监测纳升样品中的化学变化随时间的变化。电泳微分离是在一个长7厘米,40微米x 2.5厘米的矩形通道中进行的,并与50微米i.d连接。圆柱形样品引入毛细管。通过跨过分离通道的入口移动采样毛细管的出口,将通道宽度尺寸用作时间轴。分离的分析物谱带的检测通过激光诱导的荧光和基于电荷耦合器件的空间分辨检测来实现。该系统的特征是一系列的荧光素硫代氨基甲酰基氨基酸衍生物;氨基酸的检出限为<10(-8)M,荧光素的检出限为10(-9)M(425 zmol)。通过在荧光素二-β-D-吡喃半乳糖苷(FDG)(一种用于酶学研究的常用荧光底物)的酶催化水解过程中监测荧光产物的形成,证明了实现基于时间的动态微分离的能力。

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