through computer control, via both software and hardware. Each aspect plays its crucial role for successfully and accurately assessing the dynamics of single cells within a heterogeneous cell population. The reader should note that the author has chosen to describe flow cytometry first and later FACS. The author's reason for explaining the techniques this way round is primarily as this review is designed for lay readers, thus understanding the simplified equipment arrangement, prior to considering the more complex operation that takes place in the cell purification process. Briefly, the cells and/or particles start their journey in flow cytometry as suspensions. Essentially, the fluidics (flow cell) component sees the technology take a near homogenously suspended cellular population, aspirating it in laminar flow conditions, for forming a liquid jet having a near single cell diameter. This is created by the suspension fed into a flow cell accommodating a needle, centrally placed in a cylindrical chamber, having a converging base, and exit, which is coupled with a short jet stabilizing nozzle. This chamber has another input, namely, the sheath flow. With the sheath and sample flowing, the exiting sample is squeezed by the sheath flow, for it to eventually pass through both the converging architecture at the base of the chamber and subsequently flowing past the jet stabilizing exit nozzle. [2] The sheath squeezing effect, both focuses and narrows the ensuing composite jet to nearly the diameter of the cells in suspension. This process is referred to as hydrodynamic focusing. [3] This exiting fine composite jet breaking into droplets subsequently passes the point referred to as the interrogation point, where it is exposed to the laser. There are two angles in which the laser assesses these cells while they are in the jet, namely, through forward and side scatter. The forward scatter assessment process identifies the cells by way of their size. Simply put, if one was to take two objects of different shapes and sizes and place in front of a source of light, their shapes and sizes would scatter different amounts of light. This would be evident by the reflective image of the shapes created of themselves seen on some collector, placed opposite to the light source. Forward scatter works on this principle and has a detector placed on the opposite side of the laser. Similar in some respects, side scatter works with a fluorophore which is tagged using some antibody on one side while the opposite end of the antibody is attached to the molecule of interest. Note that many years of research into molecular and cell biology has given rise to the development of advanced antibodies and fluorophores which enable many cellular components to be assessed in real In this review, a brief history of this unrivaled technology, flow cytometry, is provided, highlighting its past and present advances, with particular focus on "flow cell" technologies. Flow cytometry has truly revolutionized highthroughput single cell analysis, which has treme...