Neuronal Cell Cultures

Every Cell has a Story to Tell.
Let’s Discover Yours

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Neuronal cell cultures are powerful in vitro models for investigating development, connectivity, and dysfunction of the nervous system. But to truly understand how neurons behave, you need more than structure; you need their detailed function.

Our High-Density Microelectrode Array (HD-MEA) technology captures rich, reproducible functional data at subcellular, single-cell, and network levels, providing you with scalable workflows to reveal subtle phenotypes, track maturation, and confidently screen compounds with ease and precision.

Easily capture the full story of your neurons

Our Technology

Complete the picture of your neuronal activity

Get more meaningful data on how your neurons fire, connect, and mature, going beyond standard assays with rich functional readouts at subcellular, single-cell, and network levels thanks to the 26’400 electrode per well.

Reveal hidden action potential insights

Acquire reliable action potentials, from tiniest to strongest, to reconstruct the subcellular axonal behavior of your cells. Uncover novel functional mechanisms and phenotypes others cannot see.

Sensitivity to subtle and unseen phenotypes

Biologically relevant changes are not always obvious. Detect nuanced functional differences other systems might miss, even in sparse, co-cultured or early-stage neuronal models, thanks to our high-resolution and low-noise signal acquisition.

Always at the right spot, never miss a neuron

Record high-quality signals with thousands of electrodes per well, precisely positioned beneath your cells of interest, and capture activity with unmatched resolution.

Reproducibility at the core

Neuronal cell cultures can be biologically variable, but your recordings do not have to be. See functional differences that you can trust: engineered for long-term, stable experiments and consistent signal acquisition across sessions.

Functional characterization of neuronal cultures

Perform high-resolution electrophysiological recordings across a wide range of neuronal cell cultures, encompassing diverse cell types and disease models. Thanks to the MaxOne Single-Well and MaxTwo Multi-Well HD-MEA Systems, you can reliably capture and analyze network dynamics at multiple scales, from population-level activity to single-cell behavior and even subcellular axonal signal propagation, all with high fidelity and reproducibility.

Comprehensive characterization across neuronal culture types

For every neuronal culture model, our HD-MEA systems are designed to reveal their full functional profile. A broad range of cultures can be characterized at multiple levels, from activity across the whole sample at single-cell resolution with the ActivityScan Assay, population network dynamics with the Network Assay, to electrically reconstructed axonal branches with the AxonTracking Assay, a unique capability of our HD-MEA technology.

Example dataset illustrating the multi-scale functional characterization of neuronal cell cultures recorded with MaxWell’s HD-MEAs and analyzed using MaxLab Live.

From left to right: ActivityScan Assay heatmaps display spatial patterns of spiking activity across the culture; Network Assay raster plots capture temporal dynamics of population bursts; and AxonTracking Assay axonal footprint reconstructions reveal subcellular signal propagation paths in representative neuronal cultures.

Data courtesy of multiple MaxWell Biosystems’ users.

Reproducible functional insights across neuronal models

Capture robust, reproducible neuronal phenotypes across both healthy and disease model cultures using the MaxTwo HD-MEA System. The panel below highlights spontaneous network bursting features recorded from FUJIFILM Cellular Dynamics, Inc. (FCDI, Madison, Wisconsin) human iPSC-derived control and ALS-associated mutant motor neuron cultures, co-cultured with iCell Astrocytes 2.0 (FCDI) and recorded on a MaxTwo 24-Well Plate.

Functional characterization of ALS-associated TDP-43 mutant neurons reveals robust and reproducible phenotypes.

Human iPSC-derived motor neuron lines carrying ALS-associated TARBDP mutation (M337V and Q331K; FUJIFILM Cellular Dynamics, Inc.) were co-cultured with iCell Astrocytes 2.0 and compared to a control iPSC-derived motor neuron line derived from apparently healthy neurons (AHN). All recordings were performed on a single MaxTwo 24-Well Plate. (A) Raster plots illustrate spontaneous network bursting activity, where each dot represents an action potential, and vertical groupings indicate synchronized firing (network bursts). (B) Both mutant lines exhibited consistent decreases in network synchrony, demonstrating the sensitivity and reproducibility of HD-MEA recordings across wells and genotypes. (C) Quantification of burst duration over days in vitro (DIV) reveals diverging temporal evolution of network synchrony among AHN and mutant cultures. (D) Axonal footprint reconstructions illustrate differences in axonal morphology and signal propagation between AHN and M337V neuronal cultures. (E) Axon length measurements over time demonstrate distinct growth trajectories for control versus mutant motor neuron cultures.

Data courtesy of Fujifilm Cellular Dynamics, Inc.

Relevant
Applications

Relevant Biological Models

Functional Phenotyping
Functional Phenotyping
Disease Modeling
Disease Modeling
Pharmacology & Toxicology
Pharmacology & Toxicology
Method Development
Method Development
Microphysiological Systems
Microphysiological Systems
Neurocomputing
Neurocomputing
Science
|
2025

Human neuron subtype programming via single-cell transcriptome-coupled patterning screens

Lin et al.
Nature
|
2024

A model of human neural networks reveals NPTX2 pathology in ALS and FTLD

Hruska-Plochan et al.
Science Translational Medicine
|
2023

Multiplex epigenome editing of MECP2 to rescue Rett syndrome neurons

Qian et al.
Nature Communications
|
2021

16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro

Sundberg et al.
Protocol

MaxOne+ and MaxOne Neuronal Cell Plating Protocol

Follow this easy-to-use neuronal cell plating protocol for MaxOne,ensuring optimal cell growth and attachment with clear step-by-step instructions.

Protocol

MaxTwo 24-Well Plate Neuronal Cell Plating Protocol

Maximize efficiency with this scalable protocol for high-throughput neuronal cell plating, ensuring best cell attachment and electrophysiology recordings.

Protocol

MaxTwo 6-Well Plate Neuronal Cell Plating Protocol

Maximize efficiency with this scalable protocol for high-throughput neuronal cell plating, ensuring best cell attachment and electrophysiology recordings.

Protocol

MxW - Elixirgen Application Protocol

Culturing Human iPSC-derived Mixed Neurons on Multielectrode Arrays: MaxTwo Multiwell MEA

Protocol

MxW - Neucyte Application Protocol

SynFire®iN plating protocol and chemical long-term potentiation on MaxWell Biosystems Multi-Well High-Density Microelectrode Array (HD-MEA)

Protocol

MxW - bit.bio Application Protocol

Co-culturing ioMotor Neurons and rat cortical astrocytes for HD-MEA

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Brochure

Neuronal Cell Cultures Application Brochure

Application Note

Application Note with CRL and bit.bio

Developing next-generation in-vitro phenotypic assays for Huntington's disease by combining precision reprogrammed hiPSC-derived disease models with high-density microelectrode arrays.

Application Note

Elixirgen Scientific - MxW Application Note

Long-term Characterization of Quick-NeuronTMExciatory - Human iPSC-derived Neurons with High-Density Microelectrode Arrays

Application Note

MxW - FCDI Application Note

Longitudinal Functional Profiling of HumaniPSC-derived Frontotemporal Dementia Neuronson HD-MEAs

Application Note

MxW - NeuCyte Application Note

Long-term functional characterization of SynFire®iNs and astrocytes co-cultured on MaxTwo multi-well high-density microelectrode arrays

Application Note

Nikon Application Note

Episcopic brightfield imaging of neuronal cells on high-densitymicroelectrode arrays enables prediction of cell region through AI learning

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Video

Breathe-Easy Foil MaxTwo 6-Well Plate Video Instruction

See how easy it is to apply the Breathe-Easy® sealing membranes on our MaxTwo Multiwell Plates, minimizing evaporation and ensuring optimal conditions for your sample.

Video

Dot Plating MaxOne Chip Video Instruction

Just a single tiny drop is all it takes to get the best out of your iPSC-derived neuronal cultures or primary cell cultures on MaxOne Chips.

Video

Dot Plating MaxTwo 6-Well Plate Video Instruction

Just a single tiny drop to get the best from your iPSC-derived neuronal cultures or primary cell cultures on MaxTwo Multiwell Plates.

Video

Whole Area Plating MaxOne Chip Video Instruction

Just a small drop is all it takes to get the most out of your iPSC-derived neuronal cultures or primary cell cultures on MaxOne Chips.

Video

Whole Area Plating MaxTwo 6-Well Plate Video Instructions

Just a small drop to get the best from your iPSC-derived neuronal cultures or primary cell cultures on MaxTwo Multiwell Plates.

Dr. Marcus Kaji

Weckhuysen Lab, VIB - University of Antwerp Center for Molecular Biology, Belgium

“In acute toxicity studies, the 24-Well Plates let us use less compound while increasing throughput, a huge advantage especially for novel compounds. Honestly, I couldn’t have run these experiments without the higher throughput and batch analysis combination!”

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Dr. Tetsuya Tanaka

Ricoh Biosciences, Inc., Baltimore, Maryland, USA

“Unlike other commercially available MEA systems, MaxTwo has an outstanding capability to measure and track action potentials in single neurons due to how the electrodes are arrayed in such a high density manner."

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