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基于拉链核酸探针和电化学阵列的因子 V Leiden 突变的阻抗传感检测

Impedimetric Sensing of Factor V Leiden Mutation by Zip Nucleic Acid Probe and Electrochemical Array.

机构信息

Analytical Chemistry Department, Faculty of Pharmacy, Ege University, Bornova, Izmir 35100, Turkey.

出版信息

Biosensors (Basel). 2020 Sep 7;10(9):116. doi: 10.3390/bios10090116.

Abstract

A carbon nanofiber enriched 8-channel screen-printed electrochemical array was used for the impedimetric detection of SNP related to Factor V Leiden (FV Leiden) mutation, which is the most common inherited form of thrombophilia. FV Leiden mutation sensing was carried out in three steps: solution-phase nucleic acid hybridization between zip nucleic acid probe (Z-probe) and mutant type DNA target, followed by the immobilization of the hybrid on the working electrode area of array, and measurement by electrochemical impedance spectroscopy (EIS). TArzhe selectivity of the assay was tested against mutation-free DNA sequences and synthetic polymerase chain reaction (PCR) samples. The developed biosensor was a trustful assay for FV Leiden mutation diagnosis, which can effectively discriminate wild type and mutant type even in PCR samples.

摘要

一种富含碳纳米纤维的 8 通道丝网印刷电化学阵列被用于 SNP 相关因子 V 莱顿(FV Leiden)突变的阻抗检测,该突变是最常见的遗传性血栓形成倾向形式。FV Leiden 突变检测分三个步骤进行:Zip 核酸探针(Z-探针)与突变型 DNA 靶标在溶液相中的核酸杂交,然后将杂交物固定在阵列的工作电极区域,最后通过电化学阻抗谱(EIS)进行测量。该检测方法对无突变的 DNA 序列和合成聚合酶链反应(PCR)样本进行了 TArzhe 选择性测试。开发的生物传感器是一种可靠的 FV Leiden 突变诊断方法,即使在 PCR 样本中,它也可以有效地区分野生型和突变型。

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