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Development of a Universal Probe for Electronic Microarray and Its Application in Characterization of the Staphylococcus aureus polC Gene

机译:电子芯片通用探针的开发及其在金黄色葡萄球菌polC基因鉴定中的应用

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摘要

Electronic microarray technology is an exceptionally accurate and effective technique for detecting and defining single nucleotide polymorphisms (SNPs) in DNA sequences. Target oligonucleotides are electronically addressed to a gel matrix containing streptavidin to which biotinylated polymerase chain reaction (PCR) amplicons are bound. Typically, a fluorescent-labeled reporter oligonucleotide specific for each locus of interest is hybridized and reported. We detail the development of a universal reporter system to replace the standard method that is used to detect many different sequences accurately. The universal reporter eliminates the need to synthesize specific labeled reporters for each SNP sequence thereby dramatically reducing the cost and time required for assay development. The feasibility of this approach was demonstrated by successfully analyzing eight SNPs distributed within a highly variable 1-kb region of the polC gene from six isolates of Staphylococcus aureus.
机译:电子微阵列技术是一种用于检测和定义DNA序列中单核苷酸多态性(SNP)的异常准确和有效的技术。将目标寡核苷酸电子寻址到含有链霉亲和素的凝胶基质,生物素化的聚合酶链反应(PCR)扩增子与之结合。通常,杂交并报道对每个目的基因座特异的荧光标记的报告寡核苷酸。我们详细介绍了通用报告系统的开发,以取代用于准确检测许多不同序列的标准方法。通用报告基因消除了为每个SNP序列合成特定标记报告基因的需要,从而大大降低了测定开发所需的成本和时间。通过成功分析了六个金黄色葡萄球菌分离株中polC基因高度可变的1kb区域中分布的八个SNP,证明了该方法的可行性。

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