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©2014 Baishideng Publishing Group Inc.
World J Gastroenterol. Jun 7, 2014; 20(21): 6547-6553
Published online Jun 7, 2014. doi: 10.3748/wjg.v20.i21.6547
Published online Jun 7, 2014. doi: 10.3748/wjg.v20.i21.6547
Figure 1 Representative example of the dual-priming oligonucleotide-based multiplex polymerase chain reaction.
Lane M: Amplicon size marker (Seegene Inc.,Korea); Lane 1: Negative; Lane 2: Mutant type of A2143G; Lane 3-4: Wild type; PC1: A2142G mutant positive control; PC2 : A2143G mutant positive control; NC: Negative control.
Figure 2 Detection of Helicobacter pylori and the A2143G/A2142G of the 23S rRNA gene on the basis of the dual-priming oligonucleotide-based multiplex polymerase chain reaction product in enrolled patients.
M: 100 bp Marker; A: ClaR Marker; B: A2142G Positive Marker; C: A2143G Positive Marker; NC: Negative Marker; 1-54 : Samples.
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Citation: Chung WC, Jung SH, Oh JH, Kim TH, Cheung DY, Kim BW, Kim SS, Kim JI, Sin EY. Dual-priming oligonucleotide-based multiplex PCR using tissue samples in rapid urease test in the detection of
Helicobacter pylori infection. World J Gastroenterol 2014; 20(21): 6547-6553 - URL: https://www.wjgnet.com/1007-9327/full/v20/i21/6547.htm
- DOI: https://dx.doi.org/10.3748/wjg.v20.i21.6547