Availability of purified or highly enriched fractions representing the various spermatogenic stages is a usual requirement to study mammalian spermatogenesis at the molecular level. Fast preparation of high quality testicular cell suspensions is crucial when flow cytometry (FCM) is chosen to accomplish the stage/s purification. Formerly, we reported a method to rapidly obtain good quality rodent testicular cell suspensions for FCM analysis and sorting. Using that method we could distinguish and purify early meiocytes (leptotene/zygotene stages, L/Z) from more advanced ones (pachytene, P) in guinea pig, which presents an unusually high content of early stages. Here we present an upgrade of that method with improvements that have enabled the obtainment of high-purity meiotic substages also from mouse testis, namely: • Shortening of the mechanical disaggregation time and elimination of a 25µm-filtration step, to optimize the integrity of the suspension and ensure the presence of large P cells. • Inclusion of a non-cytotoxic, DNA-specific, 488_nm-excitable vital fluorochrome (Vybrant-DyeCycle-Green [VDG], Invitrogen) instead of Hoechst 33342 (requires UV laser, which can damage nucleic acids) or propidium iodide (usually related to dead/damaged cells). As far as we know, this is the first report on the use of this fluorochrome on testicular cells.