A flow photometer which is capable of measuring simultaneously the light scattering and fluorescence of stained mammalian cells is described. An argon-ion laser serves as the light source. As individual stained cells cross the laser beam, a scattering and a fluorescence light pulse are produced. These signals are detected, amplified, and subjected to pulse-height analysis. In its simplest form, this instrument is used to gate one signal by the other, thus extending the sensitivity of the flow microfluorometry techniques developed at the Los Alamos Scientific Laboratory. Data are presented illustrating the capability of the instrument to extract the signal from the noise, in the case of weakly stained cells, and to distinguish cells in a mixed population based on a combination of these two parameters.