rpoB公司
放大器
牙龈卟啉单胞菌
生物
实时聚合酶链反应
核酸序列
底漆(化妆品)
基因
聚合酶链反应
分子生物学
遗传学
微生物学
细菌
16S核糖体RNA
化学
有机化学
作者
Soon‐Nang Park,Jae‐Yoon Park,Joong‐Ki Kook
标识
DOI:10.1007/s12275-011-1028-y
摘要
Species-specific quantitative real-time PCR (qPCR) primers were developed for the detection of Porphyromonas gingivalis. These primers, Pg-F/Pg-R, were designed based on the nucleotide sequences of RNA polymerase β-subunit gene (rpoB). Species-specific amplicons were obtained from the tested P. gingivalis strains but not in any of the other strains (46 strains of 46 species). The qPCR primers could detect as little as 4 fg of P. gingivalis chromosomal DNA. These findings suggest that these qPCR primers are suitable for applications in epidemiological studies.
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