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Biological specificity of two-photon excitation fluorescence detection method and apparatus for the

机译:双光子激发荧光检测方法的生物特异性

摘要

(57) biospecific reagent is labeled microparticles as [Abstract] bioaffinity binding solid phase, a fluorescent label, and using a fluorescence detection system based on two-photon fluorescence excitation, the analyte, labeled reagent, and the fluorescence emitted by the particles from the individual particles when suspended randomly the particles through the focal volume of the laser beam simultaneously contacted the solid phase, and focuses the two-photon excitation laser beam into the reaction suspension method of monitoring the real-time dynamics measurement method and of the end point of the biological affinity reaction suspension in biological fluids and to measure the signal. In this method, the monitored kinetically the signal to obtain information about the concentration of the analyte before the reaction is to be close to the highest point of the response. The growth rate of the signal strength is directly proportional to the concentration of the analyte, the concentration of the analyte can be expected in the initial stage of the reaction. That by the monitoring of the growth rate, it is whether will continue the reaction is more than the highest point of the response curve the concentration of the analyte, and whether higher than the binding capacity of the reagent is also predicted. According to this method, it can be completely eliminated the risk of obtaining ambiguous results in the measurement of the low and high concentrations. It is also possible that the dynamic range of the assay, to extend considerably. By combining the features of the present invention, Fast and has a large dynamic range for the samples of small volume is very fluid, a biological specimen or other cell suspensions, a single step, the separated unnecessary and biospecific method and apparatus for performing a sex test can be performed.
机译:(57)将生物特异性试剂标记为[亲和]生物亲和力的固相微粒,荧光标记,并使用基于双光子荧光激发的荧光检测系统,分析物,标记试剂以及由微粒从荧光体发射的荧光当单个粒子随机悬浮时,粒子通过激光束的焦点体积同时与固相接触,并将双光子激发激光束聚焦到反应悬浮方法中,以监测实时动力学测量方法和终点生物亲和反应悬浮在生物液体中并测量信号。在这种方法中,在反应要接近反应的最高点之前,从动力学上监测信号以获得有关分析物浓度的信息。信号强度的增长率与分析物的浓度成正比,可以在反应的初始阶段预期分析物的浓度。通过监测生长速率,可以确定反应是否将继续进行,直到被分析物的浓度超过响应曲线的最高点,并且还可以预测是否高于试剂的结合能力。根据该方法,可以完全消除在测量低浓度和高浓度时获得模棱两可的结果的风险。测定的动态范围也有可能大大扩展。通过结合本发明的特征,快速且具有大的动态范围,对于小体积的样品非常易流动,生物标本或其他细胞悬浮液,只需一步,将不必要的和生物特异性的分离方法和装置进行性交可以执行测试。

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