To avoid the well-known shortcomings of phenotyping granulocytes for t
he NA antigens using NA-specific human sera, a DNA-based method to det
ermine the NA genotype was developed. Genomic DNA was isolated from bl
ood cells or serum, amplified by polymerase chain reaction (PCR), immo
bilized on nylon membrane and genotyped using digoxigenin-labeled, seq
uence-specific oligonucleotides (SSO). The genotyping results of whole
blood samples from 54 and of serum from 20 individuals correlated per
fectly with our phenotyping using the antigen capture assay MAIGA. In
three cases with the phenotype ''NA-null'' no hybridization of the NA-
specific oligonucleotides occurred. These data show that SSO is a reli
able method for NA genotyping especially if only small volumes of bloo
d or even only serum probes are available.