MEA is an advanced electrophysiological detection technology that uses multiple microelectrodes embedded on the surface of culture plates to simultaneously monitor and record electrical signals from multiple cells. These electrodes are in close contact with the cells, allowing electrical signals generated by the cells to be transmitted through the cell-electrode interface and captured by the MEA system as analyzable data. With its efficiency, non-invasiveness, and ability for long-term continuous monitoring, MEA technology is a powerful tool for research in neuroscience, developmental biology, and drug development.
Microelectrode Array (MEA) Technology


This data set demonstrates the dose-dependent effects of Haloperidol on neuronal firing. Raster plots and associated firing parameters (for Weighted Mean Firing Rate, Number of Bursts, Burst Duration and Burst Frequency, n = 3; for Number of Network Bursts, n = 2) are presented for varying Haloperidol concentrations. At 0.1 μM, the firing activity is enhanced, while at 1 μM, the activity diminishes. At 10 μM, the firing is nearly abolished. These results are consistent with findings from Yokoi et al. (2019), where Haloperidol is known to inhibit D2 receptors at low doses and 5-HT2 receptors at high doses (Tyler et al., 2017). This confirms that the relevant receptors in our Human iPSC-Derived Dopamine Neurons are functioning normally, underscoring their utility in drug screening and neurotoxicity studies.
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