Genetic polymorphism of the human terminal complement component C7 has been studied by means of polyacrylamide gel isoelectric focussing (IEF) followed by hemolytic overlay or by immunoblotting. In Caucasians only one common allele (C7"1) with a gene frequency of 0.99 has been described, whereas in the Far East three additional common C7 allele (frequencies of 0.04-0.10) and a few very rare alleles have been reported, as reviewed (W~irzner et al. 1990b). In addition to this protein polymorphism0 a DNA polymorphism based on the restriction enzyme Taq I has been described (Coto et al. 1990).Two sandwich enzyme-linked immunosorbent assays (ELISAs) for the quantitation of human C7 have been published recently (Wfirzner et al. 1990b). One is based on a mouse monoclonal antibody (mAb), WU 4-15, the other is based on a polyclonal C7-specific IgG, as coating antibodies for ELISA-M (monoclonal) or ELISA-P (polyclonal), respectively. After introducing human sera in 1:2500 dilutions to the coated wells, the bound C7 was detected using biotinylated C7-specific IgG followed by horseradish peroxidase-labeled streptavidin and the substrate ABTS. The quantitation of C7 in 284 Caucasian individuals revealed three different ELISA patterns, namely identical results in both ELISAs, one-half or very low concentrations when ELISA-M results were compared with ELISA-P results obtained from the same sample. Comparison of these ELISA-M/ELISA-P ratios as well as results from IEF and immunoblotting, where three different staining intensities were detected using this mAb, revealed that the mAb is directed to an electrically neutral allotypic epitope on C7 (Wtirzner et al. 1990b). Since the findings conform to the Hardy-Weinberg