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Application of Impedimetric and Voltammetric Genosensor for Detection of a Biological Warfare: Anthrax

机译:阻抗和伏安基因传感器在生物战检测中的应用:炭疽病

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摘要

A strategy for the detection of anthrax, which is a potential biological weapon by using an electrochemical genosensing technology, is investigated. An alkanathiol-linked or unlabeled capture probe related to B. anthracis is immobilized onto gold or graphite electrode surface. A 101-mer anthrax target is used for hybridization. The extent of hybridization between probe and target sequences is determined by using differential pulse voltammetry (DPV) and electrochemical impedance spectrometry (EIS). EIS analysis are based on electron transfer resistance (R-ct) in the presence of [Fe(CN)(6)](3-14-) and DPV measurements are based on transduction of both guanine oxidation and Meldola's blue (MDB) reduction signal as hybridization indicator. The response of the probe-modified electrodes which was interacted with a noncomplementary sequence was the same as the responses of probe-modified surface and proved the specifity of the hybridization with the target. According to these results the developed genosensors based on EIS and DPV techniques can be employed for rapid and selective detection of B. anthracis.
机译:研究了炭疽的检测策略,炭疽是通过使用电化学基因传感技术而潜在的生物武器。与炭疽芽孢杆菌相关的链烷硫醇连接的或未标记的捕获探针固定在金或石墨电极表面上。将101聚体的炭疽靶用于杂交。探针和靶序列之间的杂交程度通过使用差分脉冲伏安法(DPV)和电化学阻抗谱(EIS)确定。 EIS分析基于[Fe(CN)(6)](3-14-)存在下的电子传递阻力(R-ct),DPV测量基于鸟嘌呤氧化和Meldola蓝(MDB)还原的转导信号作为杂交指标。与非互补序列相互作用的探针修饰电极的响应与探针修饰表面的响应相同,证明了与靶标杂交的特异性。根据这些结果,基于EIS和DPV技术开发的基因传感器可用于炭疽芽胞杆菌的快速和选择性检测。

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