猪PCR产物无标签检测比色传感器

Md. Eaqub Ali, U. Hashim, Md. Fazul Bari, T. S. Dhahi
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引用次数: 2

摘要

特异性DNA序列的选择性检测在临床诊断、病理学、遗传学[1-3]和食品分析[4,5]等领域的应用越来越广泛。聚合酶链反应(PCR)是几乎所有基于dna的检测中扩增特定序列片段的常用技术[3]。PCR的使用解决了敏感性问题和样品纯化步骤,从少量的单拷贝中产生大量DNA。然而,PCR扩增DNA的PCR后分析涉及复杂且耗时的电泳、印迹分析或测序[3]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Colorimetric sensor for label free detection of porcine PCR product
Selective detection of specific DNA sequences is increasingly getting momentum in clinical diagnosis, pathology, genetics [1–3] and food analysis [4, 5]. The polymerase chain reaction (PCR) is a commonly used technique to amplify specific sequence segment in nearly all DNA-based assays [3]. The use of PCR addresses both the sensitivity issues and sample purification steps producing a large quantity DNA from as little as single copy. However, post- PCR analysis of PCR amplified DNA involves complex and time consuming electrophoresis, blot analysis or sequencing [3].
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