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. Author manuscript; available in PMC: 2010 May 1.
Published in final edited form as: Environ Microbiol. 2009 Jan 23;11(5):1242–1253. doi: 10.1111/j.1462-2920.2008.01852.x

Table 1.

Primers employed in real time PCR analysis of selected CSE-regulated P. gingivalis genes

Gene Forward primer Reverse primer
PG1055; Tpr CCTACAGATTGGAGGTGGCT ATAGGCATGGTATGCTGCAA
PG2102; 61kDa antigen ATCGTTTGGTCTGATACGCA CTGCACGTTCAGCCTGTATT
PG2100; 63 kDa antigen ATTACAAGATGGCTGTGGCA TGCTGTCATGACTGTCCAAA
PG2008; TonB-linked receptor ATTCTTAGGAACGAGCGCAT GGGATTCCCTTGATCGAGTA
PG1286; Ferritin AGCGATCAATGACCAAATCA CACGGCATCGATAGCTTCT
PG1552; HemR GATTTGAAGCCGGAGAAGAG TAAGGCAGTACCACATTCGC
PG0111; CapK AGGCAACGGAGAAGTATCGT AAAGCACCATCAATGACGAA
PG1432; Sensor histidine kinase ACAGCTCGAACTGCATCAAC CTGCATATAAGTGCGGGCTA
PG0117; polysaccharide transport protein TCTCGAACGACCAATAGTGC CATTCTCTGCAATCGGCTTA

Primers were designed using the real-time PCR primer design software provided by GenScript (www.genscript.com/ssl-bin/app/primer). Tm of primers was 60 ±2°C (PG1286 forward primer, Tm = 56°C).