摘要
用UDG(尿嘧啶糖化酶)防PCR产物污染,以两个不同基因为靶序列检测同一病原菌和微孔板杂交-酶联显色检测 FCR产物的UDPE(UDG-Daplex PCR-EIA)技术,检测感染鼠疫菌植物50份,检出阳性35份,而常规直接培养阳性仅5份。表明UDPE技术灵敏度高、特异性强。
UDG(Uracil Deoxynucleotide Glycosidase) was used for anti- carryover PCR products.Two different of gents as target sequence were for amplification.And UDPE(UDG-Duplex PCR-EIA) in PCR products were detected by microplate hybrization and enzyme immunoassay(EIA) .50 samples of infected plants with Y.pestis were detected. 35 samples were positive. This method is high sensitive and specific.
出处
《中国地方病防治》
2000年第4期208-209,共2页
Chinese Journal of Control of Endemic Diseases