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. 2014 Aug 24;14:218. doi: 10.1186/s12866-014-0218-2

Table 6.

Real-time quantitative RT-PCR confirmation of selected genes

Locus no. a Primer sequence (5′-3′) b Product size (bp)
16S rRNA
F: TGTTACAATGGGAGGGACAAAGGG
118
R: TTACTAGCGAATCCAGCTTCACGG
PG0090
F: CAGAAGTGAAGGAAGAGCACGAAC
197
R: GTAGGCAGACAGCATCCAAACG
PG0195
F: TCCACGGCTGAGAACTTGCG
149
R: TGCTCGGCTTCCACCTTTGC
PG1545
F: CCAAACCCTCAACCACAATC
142
R: GGTACCGGCTGTGTTGAACT
PG0593
F: CGTGTGGGAGAGTGGGTATTGG
175
R: CGCCGCTGTTGCCTGAATTG
PG1089
F: CCATCGCGATCGATGATCAGGTAA
104
R: GGCATAGTTGCGTTCAAGGGTTTC
PG1019
F: TTCGCAGTATCCCATCCAAC
126
R: TCCGGCTCATAGACTTCCAA
PG1180
F: CAGTCTGCCACAGTTCACCA
124
R: CCCTACACGGACACTACCGA
PG1983
F: GCTCTGTGGTGTGGGCTATC
146
R: GGATAACAGGCAAACCCGAT
PG0885
F: CAGATCCAAATCGGGACTGA
156
R: GTAGAGCAAGCCATGCAAGC
PG1181 F: GATGAATTCGGGCGGATAAT
184
R: CCTTGAAGTGCTCCAACGAC

aBased on the genome annotation provided by TIGR (http://cmr.jcvi.org/cgi-bin/CMR/GenomePage.cgi?org=gpg).

bPrimers were designed using Primer3 program for the study except for the primers of P. gingivalis 16S rRNA and PG1089 [49], which were prepared based on the primer sequences published previously. The 16S rRNA gene was used as the reference gene for normalization. F, forward; R, reverse.