A sensitive and specific noncompetitive rat prolactin (rPRL) enzyme im
munoassay (EIA) is described. In this assay, the same rabbit anti-rPRL
antibody is both adsorbed to a solid-phase support, i.e. 96-well micr
otiter plates and conjugated covalently to peroxidase as a tracer. PRL
being sandwiched between antibody molecules, the enzymatic activity i
s thus proportional to the amount of rPRL concentration. This assay wa
s found highly specific for rat PRL and displayed a sensitivity of 12.
5 pg/well (0.125 ng/ml) of NIH-RP2 equivalents. The intra-assay and in
ter-assay coefficients of variation were less than 10% over a wide ran
ge of rPRL concentration (0.25-40 ng/ml). This rPRL-EIA permits to qua
ntify PRL in culture media or biological samples containing up to 25%
of plasma. Comparison with a radioimmunoassay revealed a good correlat
ion (r=0.984, the slope=1.04). This EIA is rapid, results being obtain
ed within 4h30 or 18h30 depending on the nature of the biological samp
les. The tracer, easily performed with a low cost enzyme, can be store
d for very long durations. Thus, this sensitive and rapid assay provid
es a valuable method for measuring rPRL.