The aim of the present study was to develop and validate a rapid assay for
genotyping of CYP1B1 codon 432-polymorphism. The described method is a sing
le tube assay and combines both rapid-cycle polymerase chain reaction (PCR)
with real-time monitoring by amplification and generation of the melting p
rofiles of an allele-specific fluorescent probe. With this method 300 sampl
es were analysed from healthy, unrelated Germans. Genotype frequency determ
ined for the mu tared allele CYP1B1*2 was 0.40. The results show that genot
yping of CYP1B1 codon 432-polymorphism with a real-time fluorescence PCR me
thod is a rapid and reliable assay for the analysis of large numbers of sam
ples.