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. 2009 Jan 14;15(2):211–218. doi: 10.3748/wjg.15.211

Table 1.

PCR primers for amplification of cagA, vacA and babA2 genes

Region Primer Nucleotide sequence Reference
cagA D008 5’-ATAATGCTAAATTAGACAACTTGAGCGA-3’ [28]
R008 5’-TTAGAATAATCAACAAACATCACGCCAT-3’
cagAFnz3 5’-AAAAGCGACCTTGAAAATTCC-3’ [29]
cagA-seqR1 5’-TAGCATAATTGTCCAATTTCGC-3’
vacA s1 VA1-F 5’-ATGGAAATACAACAAACACAC-3’ [30]
VA1-R 5’-CTGCTTGAATGCGCCAAAC-3’
vacA s1a S1A-F1 5’-TCTYGCTTTAGTAGGAGC-3’ [30]
vacA s1b SS3-F1 5’-AGCGCCATACCGCAAGAG-3’ [30]
vacA s1c S1C-F1 5’-CTYGCTTTAGTRGGGYTA-3’ [13]
vacA s2 VA1-F1 5’-ATGGAAATACAACAAACACAC-3’ [30]
vacA m1 VA3-F 5’-GGTCAAAATGCGGTCATGG-3’ [30]
VA3-R 5’-CCATTGGTACCTGTAGAAAC-3’
vacA m2 VA4-F 5’-GGAGCCCCAGGAAACATTG-3’ [30]
VA4-R 5’-CATAACTAGCGCCTTGCAC-3’
babA2 babA-F 5’-AATCCAAAAAGGAGAAAAAGTATGAAA-3’ [31]
babA-R 5’-TGTTAG TGATTTCGGTGTAGGACA-3’
babA2-Fnc1 5’-GAAAAAACATGAAAAAACACATCCTTTCAT-3’
This study
babA2-Rmn2 5’-TCTGGGTTAATGGCTTGCC-3’
1

Used with primer VA1-F.