Related Experiment Video
Updated: Jun 2, 2026

Development of a Quantitative Recombinase Polymerase Amplification Assay with an Internal Positive Control
Published on: March 30, 2015
Development of Porphyromonas gingivalis-specific quantitative real-time PCR primers based on the nucleotide sequence
Soon-Nang Park1, Jae-Yoon Park, Joong-Ki Kook
1Department of Oral Biochemistry, Chosun University, Gwangju 501-759, Republic of Korea.
Abstract:
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.
Related Concept Videos
Real Time RT-PCR
The real-time quantification of the number of amplified products is...
PCR
