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. 2014 Jan 23;20:1. doi: 10.1186/1678-9199-20-1

Table 1.

Primers and condition of amplification used in the study

Primers Primer sequence (5′-3′) Amplification condition Gene Reference
DupA1
CGTGATCAATATGGATGCTT
35 cycles: 45 s, 94°C; 45 s, 52°C and 45 s, 72°C
dupA
Gomes et al.[6]
DupA2
TCTTTCTAGCTTGAGCGA
Cag1
ATGACTAACGAAACTATTGATC
40 cycles: 1 min, 94°C; 1 min, 53°C and 1 min, 72°C
cagA
Rasmussen et al.[9]
Cag2
CAGGATTTTTGATCGCTTTATT
Hpx1a
CTGGAGARACTAAGYCCTCC
40 cycles: 1 min, 94°C; 1 min, 59°C and 1 min, 72°C
16S rRNA
Scholte et al. [12]
Hpx2
GAGGAATACTCATTGCGAAGGCGA
SA
ATGGAAATACAACAAACACAC
40 cycles: 45 s, 94°C; 45 s, 54°C and 45 s, 72°C
vacA-s
Atherton et al. [13]
SCa
CCTGARACCGTTCCTACAGC
Doorn et al. [14]
MAa
CACAGCCACTTTYAATAACGA
35 cycles at: 45 s, 94°C, 45 s, 55°C and 1 min, 72°C vacA-m Doorn et al. [14]
MB CGTCAAAATAATTCCAAGGG

•Genotype vacA: s1/m1 – strain 60190 of H. pylori (GeneBank U05676).

•Genotype vacA: s2/m2 – strain Tx30a of H. pylori (GeneBank U29401).

aR = a A or G and Y = C or T.