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Mea2100 lite system

Manufactured by MultiSciences Biotech
Sourced in Germany

The MEA2100-Lite-system is a comprehensive platform for multi-channel extracellular recordings. It provides a scalable and flexible solution for monitoring the electrical activity of various cell types, including neuronal networks, cardiomyocytes, and other electrogenic cells. The system is designed to facilitate high-quality data acquisition and analysis, enabling researchers to study the functional properties and dynamics of these cell cultures.

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3 protocols using mea2100 lite system

1

Multichannel Retinal Ganglion Cell Spike Recording

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The RGC spikes were recorded using a 60-channel MEA. Briefly, the data acquisition system (MEA2100-Lite-system; Multichannel Systems GmbH, Reutlingen, Germany) included a planar 60-channel array, an amplifier (MEA2100-60-headstage), an MCS-Lite interface board, and temperature control units (TC02 and PH01). The retinal activities were recorded with a bandpass from 1 to 3000 Hz; a gain of 1200; and a sampling rate of 25 kHz. The electrode array had 59 titanium nitride (TiN) active electrodes in an 8 × 8 grid layout on a porous polyimide foil isolator with an electrode diameter of 30 μm, inter-electrode distance of 200 μm, and a large internal reference electrode as channel 15. The impedance level was approximately 50 kΩ at 1 kHz. The amplifier was placed in a Faraday cage connected to a laboratory-made ground system. The raw trace was recorded using the online data acquisition software of the Multi Channel Suite package (Multi Channel Experimenter version 2.4.4; Multichannel Systems GmbH, Reutlingen, Germany).
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2

Extracellular Recording of Primary Neurons on MEAs

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MEAs (Multi Channel Systems, 60MEA200/10iR-Ti) consist of 59 titanium nitride (TiN) working electrodes with a diameter of 10 μm with 200 μm spacing between electrodes and one internal reference electrode. Prior to recording, MEAs were treated with oxygen plasma for 30 seconds using a PX-500 Plasma System (March Instruments), 100 μg/mL of poly-D-lysine overnight (Sigma, P0899), and 10 μg/mL Laminin (Sigma, L2020) for 2h prior to culture of primary neurons. For recording, culture medium was removed and 1 mL of warmed MEA recording solution85 (link),86 (link) was added to each MEA. Each culture was allowed to equilibrate with the MEA solution for 5 minutes in the 37°C incubator before recording. Recordings were conducted with a MEA2100-Lite-System (Multi Channel Systems) that was maintained at 37°C using the TC02 temperature controller (Multi Channel Systems). The Multi Channel Experimenter software (Multi Channel Systems) was used to record the extracellular potential at each electrode for 5 minutes using a sampling rate of 20 kHz. After recording, MEA recording solution was removed and the conditioned cell culture medium was returned to the MEA.
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3

Organoid Electrophysiology on Multi-Electrode Array

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Organoid electrical activity was measured using an MEA2100-lite system with TC01 temperature control (Multi Channel Systems), heated to 37°C. Recordings were made for 5–10 min at a frequency of 10 kHz using Multi Channel Experimenter software. Data were processed using Multi Channel Analyzer software. Raw electrode recordings were filtered sequentially with a 200 Hz second-order Butterworth high-pass filter, then a 3 kHz second-order Butterworth low-pass filter. Spikes were picked using a threshold of 5 SDs below mean voltage for each electrode.
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