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. Author manuscript; available in PMC: 2014 Jun 10.
Published in final edited form as: Virology. 2013 Nov 9;448:314–321. doi: 10.1016/j.virol.2013.10.032

Table 2.

Polymerase chain reaction primers used to target bisulfite modified DNA in order to generate amplicons of the HPV16, 18, 31 and 45 L2 and L1 genes and the cellular DAPK genes, which bracket the CpG dinucleotides numbered in Figs. 14.

HPV16-5526F AGTTCCAGGGTCTCCACAAT
HPV16-5730R GTGCGTGCAACATATTCATCCG
HPV16-7094F AAAGCTACACCCACCACCTCAT
HPV16-7443R AAATGGGCCTGGCGCTACAAA
18mod7013-F TAAATTTTTGGTTTAGGTTGGATTG
18mod7188-R AAAACATACAAACACAACAATAAATA
Bis18-6118F GGGTTAAAGGTATTGTTTGTAAAT
Bis18-6393R AAAATACCTAACAAAAAACTACTCAC
31Bis-5475F ATGGGGGTGATTTTTATTTGTATTT
31Bis-5771R ACCCTATATTATAATCCTAACACCTTTAAT
31Bis-5801F ATTTGGATTTTTTGATATATTTTTTTATAA
31Bis-6993R CATTCCCTATTATCAATACCAAAAC
31Bis-6926F AGATTTAGATTAGTTTTTATTGGGT
31Bis-7281R AAATATATATAAAAACAACATACACAACAC
45Bis-4740F GAGGTGTTTTAAATAGGGGAGGTAT
45Bis-5017R ATCCAAAAACTCATAAACTAAATTATCAAA
45Bis-6965F TTGATTTAAAGGAAAAATTTTTTTT
45Bis-7290R ATAACACCATACATACCACAAAACAC
DAPK1-1 YGGAGGATAGTYGGATYTAGTTAA
DAPK1-2 ACRAAAACACAACTAAAAAATAAATAAAAAAC