SUMMARY Renin was extracted and purified from human, dog, bog, rat, beef, rabbit and sheep kidneys. The renin "concentration" of these preparations was determined and expressed in international (Goldblatt) units by measuring the pressor effect produced by intravascular injection into normal dogs of a permanent colony. The renin "activity" was determined by bioassay, in the rat, of the angiotensin produced by incubation in vitro with renin substrate prepared from the serum of nephrectomized dogs.The rate of angiotensin formation was proportional to the concentration of renin, independent of the substrate concentration, and rather similar for renin of all seven species (mean rate =» 55 X 10 4 ng angiotensin/unit renin/16 hrs).Due to this uniformity, either of the two international reference preparations of renin (human or hog) from the World Health Organization can serve as an internal standard in the assay of renin of each of the seven species, to express their concentration in terms of the international unit.Renin substrate from hog plasma was suitable for the assay of human, dog and nog renin (mean rate = 55 X 10*). However, it reacted much more slowly with the renin of rat, beef, rabbit and sheep (mean rate = 9 X 10 Such test dogs, however, are usually not available in most laboratories and, furthermore, a relatively large dose, such as 1 unit of renin, would be required to raise the blood pressure of such a dog by 30 mm Hg.The present "indirect" assay procedure makes it possible to determine rather low concentrations; for example, 0.5 X 10~* unit of renin, the amount present in 0.005 mg of rabbit kidney. This procedure is based on the prolonged (16 hours at 38 °C) incubation of renin in vitro with its substrate and the subsequent assay of the angiotensin produced.