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首页> 外文期刊>Analytical chemistry >Automated frit inlet frit outlet flow field-flow fractionation for protein characterization with emphasis on polymeric wheat proteins
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Automated frit inlet frit outlet flow field-flow fractionation for protein characterization with emphasis on polymeric wheat proteins

机译:自动玻璃料入口玻璃料出口流场流分馏,用于蛋白质表征,重点是聚合小麦蛋白质

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摘要

A now held-flow fractionation (FFF) unit fitted with a 254-mn spacer, frit inlet (FI), and frit outlet (FO) was automated for protein analysis by addition of a system, controller, autosampler, and computer software to control pumps, sample loading, and data capture. Standard molecular size marker proteins and polymeric wheat storage protein extracts were used to assess the performance of the automated unit. Optimum resolution for these proteins was obtained. with a sample inlet now of 0.2 mL/min, a hit inlet now (recirculating) of 1.4 mL/min, and a cross-now (recirculating) of 5 mL/min using 0.05 M acetic acid containing 0.002% FL-70 as a carrier. Use of the FIFO FFF eliminates the requirement for stop-flow relaxation and pressure balancing, results in better reproducibility, and generates a 7-10-fold increase in sensitivity at the detector by concentrating fractions eluting from the channel. These improvements resulted in superior resolution of polymeric wheat protein fractions compared to those obtained previously using a standard channel with manual load and stop-now relaxation, allowing accurate integration of peak or size range areas. Automation of this system allows unattended sample fractionation and hence markedly increases potential for sample throughput. [References: 27]
机译:现在,通过添加系统,控制器,自动进样器和计算机软件来控制配备了254-mn垫片,玻璃料入口(FI)和玻璃料出口(FO)的固定流分馏(FFF)单元,以自动进行蛋白质分析。泵,样品加载和数据采集。使用标准分子大小标记蛋白和小麦聚合贮藏蛋白提取物来评估自动化装置的性能。获得了这些蛋白质的最佳分离度。使用0.2 mL / min的样品进样口,1.4 mL / min的瞬时进样(再循环)和使用0.002%FL-70的0.05 M乙酸作为样品的瞬时进样(再循环)为5 mL / min。载体。 FIFO FFF的使用消除了对停止流松弛和压力平衡的要求,从而实现了更好的重现性,并且通过浓缩从通道洗脱的馏分,使检测器的灵敏度提高了7-10倍。与以前使用手动加载和立即停止松弛的标准通道获得的那些相比,这些改进导致聚合小麦蛋白级分的分离度更高,从而可以准确整合峰或大小范围区域。该系统的自动化可实现无人值守的样品分离,因此显着提高了样品通量的潜力。 [参考:27]

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