The understanding of cellular Cd 2? accumulation and toxicity is hampered by a lack of fluorescent indicators selective for intracellular free Cd 2? ([Cd 2? ] i). In this study, we used depolarized MIN6 mouse pancreatic beta cells as a model for evaluating [Cd 2? ] i detection with commercially available fluorescent probes, most of which have been traditionally used to visualize [Ca 2? ] i and [Zn 2? ] i. We trialed a panel of 12 probes including fura-2, FluoZin-3, Leadmium Green, Rhod-5N, indo-1, Fluo-5N, and others. We found that the [Zn 2? ] i probe FluoZin-3 and the traditional [Ca 2? ] i probe fura-2 responded most consistently and robustly to [Cd 2? ] i accumulation mediated by voltage-gated calcium channels. While selective detection of [Cd 2? ] i by fura-2 required the omission of Ca 2? from extracellular buffers, FluoZin-3 responded to [Cd 2? ] i similarly in the presence or absence of extracellular Ca 2?. Furthermore, we showed that FluoZin-3 and fura-2 can be used together for simultaneous monitoring of [Ca 2? ] i and [Cd 2? ] i in the same cells. None of the other fluorophores tested were effective [Cd 2? ] i detectors in this model. Keywords MIN6 Á Cadmium Á Leadmium Green Á Voltage-gated calcium channel Á Metal toxicity