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. 2002 Jan;40(1):259–261. doi: 10.1128/JCM.40.1.259-261.2002

TABLE 1.

Primers used for detection of 23S rRNA gene point mutations in H. pylori isolates from patients in China

Sequence detected or purpose Primer Nucleotide sequence Location (size [bp]) of PCR producta Annealing temp (°C)
23S rRNA 5gb 5′-TCAGGGTGATGGACTGC-3′ 1027–2665 (1,639) 56
ZGE23b 5′-CACAGGCCAGTTAGCTA-3′
A2142 G 5gb 5′-TCAGGGTGATGGACTGC-3′ 1027–2530 (1,504) 60
DP4b 5′-AGGTCCACGGGGTCTTC-3′
A2143G 5gb 5′-TCAGGGTGATGGACTGC-3′ 1027–2531 (1,505) 59
DP5b 5′-AAGGTCCACGGGGTCTC-3′
A2142C 5gb 5′-TCAGGGTGATGGACTGC-3′ 1027–2535 (1,509) 65
DP6 5′-AGTAAAGGTCCACGGGGTCTTG-3′
Sequencing 2451-F 5′-TCAACCAGAGATTCAGT-3′ 2451–2665 (215) 50
ZGE23b 5′-CACAGGCCAGTTAGCTA-3′
a

Primer positions are according to the 23S rRNA sequence published by Taylor and colleagues (13).

b

The primer name and sequence are the same as those reported by Taylor et al. (13).