Abstract
Non-specific esterases of the normal mouse epididymis were studied by the .alpha.-naphthyl acetate (.alpha.-NA) and 5-bromoindoxyl acetate (5-BIA) methods and by these techniques in combination with inhibitors. Several esterase isozymes are present in the epididymis. The .alpha.-NA method produces a strong reaction to at least 1 isozyme more than is demonstrable by 5-BIA. The latter technique distinguishes between different cells which show identical reaction to .alpha.-NA. The use of inhibitors confirms these differences. The techniques used enable localization of the cells or origin of various isoenzymes in a complex organ. A basis for studies on the genetical control of cell function is provided.