机构地区: 深圳出入境检验检疫局
出 处: 《动物医学进展》 2009年第7期6-9,共4页
摘 要: 旨在建立实时荧光定量PCR检测布鲁菌的方法。经选取高度保守的具布鲁菌属特异性的BSP31基因设计了一对引物及探针,并采用矩阵法优化反应体系,筛选出引物、探针、dNTP和Mg2+最优浓度配比,同时进行了特异性和灵敏性试验,建立了实时荧光定量PCR检测布鲁菌的方法。该方法可用于对布鲁菌病普查监测及进出境动物及其产品的检验检疫。 This article was purposed of detection of Brucella spp by real-time PCR. A probe and a pair of primers were designed with BSP31 gene of Brucella, which is conversed domain in Brucella spp. The assay was optimized though matrix method, choseing the best concentration of the primers, probe, dNTP and Mg^2+. The specificity and sensitivity of the assay were tested. This method can be used for general investigation of brucellosis in agriculture departments,and quarantine of entry-exit animals and their products.