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首页> 外文期刊>Analytical Letters >Studies on the Toluidine Blue Dimer as a Fluorescence Probe for Protein Assays
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Studies on the Toluidine Blue Dimer as a Fluorescence Probe for Protein Assays

机译:甲苯胺蓝二聚体作为蛋白质检测荧光探针的研究

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A spectrofiuorometric method was developed for the determination of total serum protein by exploring toluidine blue (TB) as the fluorescence probe.The fluorescence intensity of TB at 648 nm was significantly quenched in the presence of sodium dodecylbenzene sulfonate (SDBS) by forming a dimer of the dye,which can afterwards reconvert to monomer when proteins were added accompanied by the recovery of the fluorescence.This might be attributed to the modulated transferring of the dimer-monomer equilibrium of TB in the anionic surfactant caused by the addition of protein.A linear calibration graph was obtained in the range of 0.5-50mg/l BSA,with a detection limit of 0.15 mg/l and a RSD of 1.3% (n= 11,5.0 mg/1 BSA).Total proteins in human serums were analyzed by using the present procedure and the results agreed well with those obtained by the Biuret method.
机译:建立了用荧光探针法测定血清总蛋白的分光光度法。在十二烷基苯磺酸钠(SDBS)存在下,通过形成二聚体二聚体,显着猝灭了648nm处TB的荧光强度。这种染料可以在添加蛋白质后随荧光的恢复而转化为单体,这可能是由于蛋白质的添加导致了阴离子表面活性剂中TB的二聚体单体平衡的调节转移。在0.5-50mg / l BSA范围内获得校正图,检出限为0.15mg / l,RSD为1.3%(n = 11,5.0 mg / 1 BSA)。使用本程序,结果与通过Biuret方法获得的结果非常吻合。

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