Genotyping of the PXR A11156C polymorphism with locked nucleic acid containing fluorogenic probes

In order to determine the genotype of the PXR A11156C polymorphism, we developed a real-time PCR fluorescence resonance energy transfer (FRET) assay. Although homozygotes could be discriminated unequivocally, separate melting peaks could not be obtained in putative heterozygote genotypes. To improve...

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Veröffentlicht in:The hematology journal : the official journal of the European Haematology Association 2005-04, Vol.5 (2), p.72-74
Hauptverfasser: Op den Buijsch, R A M, de Vries, J E, Loots, W J G, Landt, O, Wijnen, P A H M, van Dieijen-Visser, M P, Bekers, O
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Sprache:eng
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Zusammenfassung:In order to determine the genotype of the PXR A11156C polymorphism, we developed a real-time PCR fluorescence resonance energy transfer (FRET) assay. Although homozygotes could be discriminated unequivocally, separate melting peaks could not be obtained in putative heterozygote genotypes. To improve the discriminative power of the sensor probe, two routes were followed. The first was to shorten the sensor probe and the second route was to modify the sensor probe with a locked nucleic acid (LNA) on the polymorphic position.
ISSN:1470-269X
1466-4860
1473-1150
DOI:10.1038/sj.tpj.6500299