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Electrochemical Behaviors of Methylene Blue on DNA Modified Electrode and Its Application to the Detection of PCR Product from NOS Sequence

机译:亚甲蓝在DNA修饰电极上的电化学行为及其在NOS序列PCR产物检测中的应用

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摘要

An electrochemical DNA biosensor for the detection of NOS gene sequences from genetically modified organisms (GMOs) is presented in this paper. Single-stranded DNA (ssDNA) was covalently attached through the carboxylate ester formed by the 3′-hydroxy end of the DNA with the carboxyl of a mercaptoacetic acid self-assembled monolayer-modified gold electrode using N-hydroxysuccinimide (NHS) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDC) as linkers. The electrochemical behavior of methylene blue (MB) on the ssDNA and dsDNA modified gold electrode were carefully studied. Compared with ssDNA/Au electrode, an increase of redox peak current of MB on dsDNA/Au electrode was found, which could be further used for monitoring the recognition of DNA hybridization. Based on this result, the polymerase chain reaction (PCR) product of the common inserts NOS terminator from real GMOs samples was detected successfully.
机译:本文提出了一种用于检测转基因生物(GMO)NOS基因序列的电化学DNA生物传感器。单链DNA(ssDNA)通过DNA的3'-羟基末端与巯基乙酸自组装单层修饰金电极的羧基形成的羧酸酯共价连接,使用N-羟基琥珀酰亚胺(NHS)和N- (3-二甲基氨基丙基)-N'-乙基碳二亚胺盐酸盐(EDC)作为连接基。仔细研究了亚甲基蓝(MB)在ssDNA和dsDNA修饰的金电极上的电化学行为。与ssDNA / Au电极相比,发现dsDNA / Au电极上MB的氧化还原峰电流增加,可进一步用于监测DNA杂交的识别。基于此结果,成功地检测了来自真实GMO样品的常见插入片段NOS终止子的聚合酶链反应(PCR)产物。

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