Cell counting is one of the most frequently performed tasks in cell biology workflows, used when preparing cells for culture, passaging, transfection, gene editing or assay development. Despite this, many laboratories continue to rely on manual counting using hemocytometers, a technique that has changed little in more than a century. While widely used, manual counting can be time consuming, labor intensive and susceptible to user-to-user variation, meaning the results often depend on individual judgement, particularly when assessing cell viability and morphology.
Alternative technologies offer better accuracy and throughput but they also have their own limitations. For example, resistive pulse sensing systems can process large numbers of cells quickly but provide limited information about cell health and morphology. In contrast, although flow cytometry delivers highly detailed data, it often requires specialized expertise, significant capital investment and dedicated laboratory space. As a result, many researchers face a compromise between simplicity, speed, accuracy and the depth of information available from each measurement.