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A nanoparticle-based bio-barcode assay for ultrasensitive detection of ricin toxin.

机译:基于纳米颗粒的生物条形码检测法,用于蓖麻毒素的超灵敏检测。

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摘要

The ultrasensitive bio-barcode amplification assay (BCA) technique was developed for the specific detection of the A chain of ricin toxin. The target antigen A chain was first captured by gold nanoparticles (GNPs) coated with polyclonal antibodies. Magnetic microparticles (MMPs) coated with A chain monoclonal antibody were then added to form a sandwich immuno-complex. After the immuno-complex was formed, signal DNA annealed to DNA strands covalently bound to the GNPs were released by heating and characterized by PCR and real-time fluorescence PCR. A detection limit of 1 fg/ml was measured for A chain, six orders of magnitude more sensitive than that of conventional antigen-capture ELISA. The coefficient of variation (CV) of intra-assay and inter-assay ranged from 3.39% to 6.84%. The BCA can detect the A chain in milk and water mimic samples. In the following work it is demonstrated that this assay is a highly sensitive method for the detection of ricin proteins that could be adapted to measure other proteins.
机译:开发了超灵敏生物条形码扩增测定(BCA)技术,用于特异性检测蓖麻毒素的A链。首先通过包被多克隆抗体的金纳米颗粒(GNP)捕获靶抗原A链。然后加入涂有A链单克隆抗体的磁性微粒(MMP),形成夹心免疫复合物。形成免疫复合物后,通过加热释放退火至与GNP共价结合的DNA链的信号DNA,并通过PCR和实时荧光PCR进行表征。 A链的检出限为1 fg / ml,比常规抗原捕获ELISA的灵敏度高六个数量级。批内和批间变异系数(CV)为3.39%至6.84%。 BCA可以检测牛奶和水模拟样品中的A链。在随后的工作中,证明了该测定法是检测蓖麻毒蛋白的一种高度灵敏的方法,该蓖麻蛋白可以适用于测量其他蛋白质。

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