In order to produce antibody for use in radioimmunoassay of gastrin in physiological concentration, four rabbits of New Zealand white were immunized with synthetic human gastrin-17-I conjugated to hemocyanin with EDC. Among them, only one rabbit produced antibody that could bind 50% of 125I-gastrin at a final dilution of 1:25,000. 125I-gastrin was prepared with synthetic human gastrin-17-I and NaI125 by lactoperoxidase technique. The product was then purified on a column of Sephadex Gl5/G5O (7:3, w/w) followed by a column of DEAE sephadex A-25. The specific radioactivity of the purified 125I-gastrin was in the range of 347-1429 μCi/nmole when determined by the self-displacement method. The effective affinity constant (Keff), total binding sites (N), heterogeneity index (α) and average affinity constant (K0) of the anti-gastrin serum calculated from Scatchard plot as well as Sips plot were 1.77 X 1011/M, 255 nM, 0.84 and 0.79 X 1011/M, respectively. When radioimmunoassay was performed with the anti-gastrin serum, it was confirmed that the mean concentration of gastrin immunoreactivity in plasma was increased by feeding in humans and rats, and also increased by bombesin administration in rats. The results indicate that the anti-gastrin serum produced in the present investigation is suitable for radioimmunological determination of gastrin in physiological concentration.