Brain Slices

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

Get in Touch
Get in Touch
Copyright by Gabriel Luna, Kosik Lab

Brain slices offer a powerful ex vivo model to study defined brain regions and circuits with both physiological relevance and experimental control. Traditional techniques such as imaging and patch-clamp provide invaluable mechanistic insights but are often limited in scale, speed, or resolution.  

Our High-Density Microelectrode Array (HD-MEA) technology delivers precise spatial localization for recording and stimulation, enabling detailed dissection of neuronal circuits across distinct compartments, thanks to its high electrode density. Capture rich, reproducible data at subcellular, single-cell, and network levels across the full spectrum of brain oscillatory activity, allowing detection of subtle functional differences other systems may miss.

Redefining functional electrophysiology for brain slices

Our Technology

Uncover functional insight across all scales

Capture circuit dynamics across the entire brain slice, from single-neuron spikes to the full range of brain oscillations, leveraging the signal quality and high spatial and temporal resolution of our HD-MEA technology.

Always on target, never miss an event

Dissect activity within and across brain regions using a streamlined setup; without the need for complex rigs. With 26’400 electrodes, precisely target specific areas to capture key events and subtle functional differences, recording exactly where it matters every time.

Scale up your electrophysiology workflow

Run high-throughput slice experiments with our platform featuring the first-ever perfusion system optimized for the MaxTwo Multi-Well HD-MEA System, maintaining slice health and signal quality and fidelity across wells.

Probe target brain regions with precise stimulations

Activate defined circuits or test plasticity mechanisms using flexible stimulation paradigms, from simple pulses to complex, customizable protocols, delivered with precise spatial and temporal control.

Optimized light stimulation for your studies

Perform high-resolution optogenetics experiments with our HD-MEA technology, optimized to reduce optical artifacts while preserving signal quality.

Functional characterization of brain slices

Perform high-resolution recordings from freshly prepared slices for acute recordings and organotypic brain slices for longitudinal recordings, thanks to the MaxOne Single-Well and MaxTwo Multi-Well HD-MEA Systems. With 26,400 flexibly controlled electrodes per well, precisely record from your region(s) of interest and capture action potentials as well as local field potentials (LFPs) and the full spectrum of brain oscillations.

Recording of extracellular action potentials in cerebellum slices

Identify functionally active regions in cerebellar slices by mapping spike amplitudes across the tissue with high spatial resolution. This enables rapid localization of high-activity regions and quantitative comparison of spike amplitudes across cerebellar layers.

Acute extracellular recordings from cerebellum slices.

Left: Brightfield image of an acute cerebellar slice positioned on the MaxOne HD-MEA chip.

Right: Spike amplitude map from the ActivityScan Assay, derived from extracellular recordings, highlighting spatially localized high-amplitude activity within distinct cerebellar lobules.

Chemically induced epileptiform activity across multiple brain regions

Take full advantage of the large electrode array on the MaxOne Single-Well and MaxTwo Multi-Well HD-MEA System to monitor chemically induced epileptiform activity simultaneously in hippocampus and cortex. In the panel below, electrical events resembling epileptic states were observed in the hippocampus and cortex of a freshly prepared brain slice treated with 4-aminopyridine.

Epileptiform activity in acute brain slice treated with 4-aminopyridine.

Top: Acute hippocampal brain slice positioned on a MaxOne HD-MEA Chip.

Bottom: Spatially distributed epileptiform activity with local field potential traces illustrating abnormal events in hippocampus and cortex following 4-aminopyridine treatment.

Courtesy of Prof. Ed Mann, University of Oxford.

Relevant
Applications

Relevant Biological Models

Functional Phenotyping
Functional Phenotyping
Method Development
Method Development
Disease Modeling
Disease Modeling
Pharmacology & Toxicology
Pharmacology & Toxicology
No items found.
No items found.
No items found.
No items found.
No items found.
No items found.
No items found.
未找到任何物品。
以前
下一步