7 The second set (cla18, cla3) was used to do 3′-mismatch PCR to detect A2142C point mutation. In this case, if the gene was of wild type there was no fragment, and if the A2142C point mutation took place, a 700 bp fragment was produced.12 Polymerase chain reaction condition was as follows for the amplification of the 1400 bp fragment: reactions were carried out in Primus thermo cycler (MWG-Biotech, Germany) in 50 μl mixtures containing 25 μl PCR master mix (CinnaGen Inc, Iran), 19 μl sterile deionized water, two μl template DNA and two μl of each oligonucleotide primer (4 μl totally). Initial denaturation Inhibitors,research,lifescience,medical at 94°C

for five min followed by 30 cycles of denaturation at 94°C for one min, annealing for one min at 58°C, extension at 72°C for one min. The final extension step was extended to five min at 72°C. The RFLP protocol was as follows: 10 μl of the 1400 bp fragment was added to two PCR microtubes, and five units of each enzyme was added to the micritubes and incubated at 37°C for 16 hours. 3′-mismatch Inhibitors,research,lifescience,medical PCR condition was as follow: Inhibitors,research,lifescience,medical reactions were carried out in Primus thermo cycler (MWG-Biotech, Germany) in 25 μl mixtures containing 12 μl PCR master mix (CinnaGen Inc, Iran), 10 μl sterile

deionized water, one μl template DNA and one μl of each oligonucleotide primer. Initial denaturation Inhibitors,research,lifescience,medical at 94°C for five min followed by 30 cycles of denaturation at 94°C for one min, annealing for one min at 55°C, extension at 72°C for one min. The final extension step was extended to five min at 72°C. Electrophorsis The PCR products were separated on 1.5% and the PCR-RFLP products were separated on 2% agarose gels Inhibitors,research,lifescience,medical (Cinna gen, Iran) after being stained with ethidium bromide (Merck, Germany) in TBE 1X (Tris/borate/EDTA) buffer under 100 volts electricity flow. Bands were visualized under UV gel documentation and photographed. Results Twenty out of 63 (31.7%) of the H. pylori isolates were resistant

to clarithromycin. There was no significant relation between gender, age or the history of antibiotic consumption by the patients and resistance to calrithromycin. All of the 20 ClaR isolates had at least one of the three common point mutation in 23s rRNA gene, while none of the ClaS isolates had such a point mutation (table 2). Table2 The frequency and (rate) Histamine H2 receptor of clarithromycin susceptibility test for H. pylori isolates in both resistant and sensitive isolates in Kerman, Iran. All of the 63 H. pylori isolates were positive for the 1400 bp fragment (http://www.selleckchem.com/products/arq-197.html figure1). Fifteen percent of the ClaR isolates (three out of 20 isolates) had the A2143G point mutation (figure 2). There was a significant relation between the gender of the patients and the A2143G point mutation. Three out of 38 (7.