A simple, rapid and reliable method has been developed for assessing t
he number and viability of cells, as well as cell size, in suspension
culture by the use of flow cytometry. Propidium iodide exclusion is us
ed for viability determination and fluorescent beads serve as an inter
nal standard for cell enumeration. The main advantages of this method
are its ability to handle a large number of samples with a high degree
of precision and its specificity in detecting viable cells quantitati
vely in a heterogeneous culture of living and dead cells and debris. T
he method shows only a fraction of the variation found in the haemacyt
ometer/trypan blue counting method due to its very low operator depend
ence.