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New Detection Method of Biological Targets Based on HTS SQUID and Magnetic Marker

机译:基于HTS SQUID和磁标记的生物目标检测新方法

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We developed improved methods of liquid-phase detection of biological targets using HTS SQUID and Brownian relaxation of magnetic markers. In a real sample, the aggregation and precipitation of free markers deteriorate their Brownian relaxation and cause so-called blank signals. In order to solve this problem, we developed two methods. First, we introduced a reaction field Bre during the binding reaction between the markers and targets. Using this method, we could obtain a strong signal from the bound markers without increasing the aggregation of the free markers. Next, we introduced a field-reversal method in the measurement procedure in order to differentiate the signal from the markers in suspension from that from the precipitated markers. Using this procedure, we could eliminate the signal from the precipitated markers. Then, we detected biotin molecules by using these methods. The biotins were immobilized on the surfaces of large polymer beads with diameters of 3.3 μm and were detected with streptavidin-conjugated magnetic markers. The minimum detectable molecular number concentration was 1.8×10^(-19) mol/ml, indicating the high sensitivity of the present method.
机译:我们开发了使用HTS SQUID和磁性标记的布朗弛豫进行液相检测生物目标的改进方法。在真实样品中,游离标记的聚集和沉淀会破坏其布朗弛豫,并导致所谓的空白信号。为了解决这个问题,我们开发了两种方法。首先,我们在标记物与靶标之间的结合反应过程中引入了一个反应场Bre。使用这种方法,我们可以从结合的标记物获得强信号,而不会增加游离标记物的聚集。接下来,我们在测量过程中引入了一种场反转方法,以区分悬浮中的标记物信号与沉淀的标记物信号。使用此过程,我们可以消除沉淀的标记物产生的信号。然后,我们使用这些方法检测了生物素分子。将生物素固定在直径为3.3μm的大聚合物珠的表面上,并用抗生蛋白链菌素共轭的磁性标记进行检测。最小可检测分子浓度为1.8×10 ^(-19)mol / ml,表明本方法灵敏度高。

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