The ABO blood group is the most important blood group system in transfusion medicine. In addition to the normal levels of ABO antigen expression, A(el) and B-el represent the two major blood types that have a weak expression of the A or B antigens on red blood cells. Due to the fact that typing of A(el) and Bel by conventional serological methods is time consuming and sometimes gives false-positive and false-negative results, it is warranted to develop an additional technique for the identification of A(el) and B-el individuals. Through genetic analysis we have previously identified A(el) as possessing an A allele with IVS6+5G -> A mutation (Transfusion 2003;43:1138-1144) and B-el as possessing a B gene with 502C -> T mutation in Taiwan (Vox Sanguinis 2003;85:216-220). Hence, real-time PCR-based genotyping methods were developed in this study to facilitate the detection of A(el) and B-el. For genotyping of A(el) and B-el, the region of mutations was PCR amplified and subjected to the LightCycler (LC) real-time PCR assay using LC Red640-labeled hybridization probe. Melting curve analysis was performed to determine the melting temperature T-m that was used for genotype detection of A(el) and B-el blood types. For A(el) genotyping, the melting curve of the normal control appears as one peak at 59.19 +/- 0.07 degrees C (mean +/- SE) and that of A(el) appears as 2 peaks at 59.21 +/- 0.07 degrees C and 64.39 +/- 0.07 degrees C, corresponding to the O and A(el) alleles, respectively. For B-el genotyping, the melting curve of the normal control appears as one peak at 67.99 +/- 0.11 degrees C and that of B-el appears as 2 peaks at 59.99 +/- 0.12 degrees C and 68.1 +/- 0.13 degrees C, corresponding to the B-el and O alleles, respectively. This genotyping method was shown to be accurate, based on automated sequencing of the PCR-amplified products. It takes only 90 min to perform this genotyping test. Detecting the A(el) and B-el blood types by combined LC-PCR and melting-curve analysis is a rapid, reliable, and easy method.