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cytoview mea plates with 16 electrodes per well  (Axion BioSystems)

 
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    Axion BioSystems cytoview mea plates with 16 electrodes per well
    Cytoview Mea Plates With 16 Electrodes Per Well, supplied by Axion BioSystems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cytoview+mea+plates+with+16+electrodes+per+well/24+well++with+16+electrodes++plates/pmc12152501-315-19-22
    Average 90 stars, based on 1 article reviews
    cytoview mea plates with 16 electrodes per well - by Bioz Stars, 2026-08
    90/100 stars

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    cytoview mea plates with 16 electrodes per well  (Axion BioSystems)
    90
    Axion BioSystems cytoview mea plates with 16 electrodes per well
    Cytoview Mea Plates With 16 Electrodes Per Well, supplied by Axion BioSystems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cytoview+mea+plates+with+16+electrodes+per+well/24+well++with+16+electrodes++plates/pmc12152501-315-19-22
    Average 90 stars, based on 1 article reviews
    cytoview mea plates with 16 electrodes per well - by Bioz Stars, 2026-08
    90/100 stars
    		  Buy from Supplier
    48-well cytoview mea plates with 16 poly-3,4-ethylendioxythiophen (pedot) electrodes per well  (Axion BioSystems)
    90
    Axion BioSystems 48-well cytoview mea plates with 16 poly-3,4-ethylendioxythiophen (pedot) electrodes per well
    ( A ) Histogram and scatter plot show distribution of number of active synapses of WT neurons cultured in media with 2 mM Ca +2 to ensure neuronal firing. AP-evoked glutamate release calculated as evoked probability (left) and spontaneous glutamate release calculated as spontaneous frequency (right), respectively. ( B ) Histogram and scatter plot show distribution of number of active synapses of Cdr1as-KO neurons cultured in media with 2 mM Ca +2 to ensure neuronal firing. AP-evoked glutamate release calculated as evoked probability (left) and spontaneous glutamate release calculated as spontaneous frequency (right), respectively. ( C ) Scheme of the Multi-electrode Array recording protocol (Axion Biosystems, <t>CytoView</t> <t>MEA</t> 48, “Methods”). Second panel: representative image of cultured neurons DIV14 in a recording well. white: electrodes, red: mCherry reporter. Third panel: schematic representation of output data, extracellular field potentials and neuronal network activity. AP: Adaptative threshold 6 SD. Sampling frequency 12.5 kHz. Active electrode selection criteria 5 spikes/minute. ( D ) Mean Firing Rate: Total number of spikes per single electrode divided by the duration of the analysis (600 s), in Hz. Each column represents recordings from a single biological replicate. Each dot represents recordings from a single electrode. ( E ) Example raw spikes from multi electrodes Array recording: 100 ms raw spikes of WT and Cdr1as-KO neurons DIV21. Each row represents one independent electrode (black bars).
    48 Well Cytoview Mea Plates With 16 Poly 3,4 Ethylendioxythiophen (Pedot) Electrodes Per Well, supplied by Axion BioSystems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cytoview+mea+plates+with+16+electrodes+per+well/24+well++with+16+electrodes++plates/pmc11239925-512-5-15
    Average 90 stars, based on 1 article reviews
    48-well cytoview mea plates with 16 poly-3,4-ethylendioxythiophen (pedot) electrodes per well - by Bioz Stars, 2026-08
    90/100 stars
    		  Buy from Supplier
    cytoview 24-well mea plates with 16 electrodes per well  (Axion BioSystems)
    90
    Axion BioSystems cytoview 24-well mea plates with 16 electrodes per well
    ( A ) Histogram and scatter plot show distribution of number of active synapses of WT neurons cultured in media with 2 mM Ca +2 to ensure neuronal firing. AP-evoked glutamate release calculated as evoked probability (left) and spontaneous glutamate release calculated as spontaneous frequency (right), respectively. ( B ) Histogram and scatter plot show distribution of number of active synapses of Cdr1as-KO neurons cultured in media with 2 mM Ca +2 to ensure neuronal firing. AP-evoked glutamate release calculated as evoked probability (left) and spontaneous glutamate release calculated as spontaneous frequency (right), respectively. ( C ) Scheme of the Multi-electrode Array recording protocol (Axion Biosystems, <t>CytoView</t> <t>MEA</t> 48, “Methods”). Second panel: representative image of cultured neurons DIV14 in a recording well. white: electrodes, red: mCherry reporter. Third panel: schematic representation of output data, extracellular field potentials and neuronal network activity. AP: Adaptative threshold 6 SD. Sampling frequency 12.5 kHz. Active electrode selection criteria 5 spikes/minute. ( D ) Mean Firing Rate: Total number of spikes per single electrode divided by the duration of the analysis (600 s), in Hz. Each column represents recordings from a single biological replicate. Each dot represents recordings from a single electrode. ( E ) Example raw spikes from multi electrodes Array recording: 100 ms raw spikes of WT and Cdr1as-KO neurons DIV21. Each row represents one independent electrode (black bars).
    Cytoview 24 Well Mea Plates With 16 Electrodes Per Well, supplied by Axion BioSystems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cytoview+mea+plates+with+16+electrodes+per+well/24+well++with+16+electrodes++plates/pmc08087674-129-0-9
    Average 90 stars, based on 1 article reviews
    cytoview 24-well mea plates with 16 electrodes per well - by Bioz Stars, 2026-08
    90/100 stars
    		  Buy from Supplier

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    ( A ) Histogram and scatter plot show distribution of number of active synapses of WT neurons cultured in media with 2 mM Ca +2 to ensure neuronal firing. AP-evoked glutamate release calculated as evoked probability (left) and spontaneous glutamate release calculated as spontaneous frequency (right), respectively. ( B ) Histogram and scatter plot show distribution of number of active synapses of Cdr1as-KO neurons cultured in media with 2 mM Ca +2 to ensure neuronal firing. AP-evoked glutamate release calculated as evoked probability (left) and spontaneous glutamate release calculated as spontaneous frequency (right), respectively. ( C ) Scheme of the Multi-electrode Array recording protocol (Axion Biosystems, CytoView MEA 48, “Methods”). Second panel: representative image of cultured neurons DIV14 in a recording well. white: electrodes, red: mCherry reporter. Third panel: schematic representation of output data, extracellular field potentials and neuronal network activity. AP: Adaptative threshold 6 SD. Sampling frequency 12.5 kHz. Active electrode selection criteria 5 spikes/minute. ( D ) Mean Firing Rate: Total number of spikes per single electrode divided by the duration of the analysis (600 s), in Hz. Each column represents recordings from a single biological replicate. Each dot represents recordings from a single electrode. ( E ) Example raw spikes from multi electrodes Array recording: 100 ms raw spikes of WT and Cdr1as-KO neurons DIV21. Each row represents one independent electrode (black bars).

    Journal: EMBO Reports

    Article Title: miR-7 controls glutamatergic transmission and neuronal connectivity in a Cdr1as-dependent manner

    doi: 10.1038/s44319-024-00168-9

    Figure Lengend Snippet: ( A ) Histogram and scatter plot show distribution of number of active synapses of WT neurons cultured in media with 2 mM Ca +2 to ensure neuronal firing. AP-evoked glutamate release calculated as evoked probability (left) and spontaneous glutamate release calculated as spontaneous frequency (right), respectively. ( B ) Histogram and scatter plot show distribution of number of active synapses of Cdr1as-KO neurons cultured in media with 2 mM Ca +2 to ensure neuronal firing. AP-evoked glutamate release calculated as evoked probability (left) and spontaneous glutamate release calculated as spontaneous frequency (right), respectively. ( C ) Scheme of the Multi-electrode Array recording protocol (Axion Biosystems, CytoView MEA 48, “Methods”). Second panel: representative image of cultured neurons DIV14 in a recording well. white: electrodes, red: mCherry reporter. Third panel: schematic representation of output data, extracellular field potentials and neuronal network activity. AP: Adaptative threshold 6 SD. Sampling frequency 12.5 kHz. Active electrode selection criteria 5 spikes/minute. ( D ) Mean Firing Rate: Total number of spikes per single electrode divided by the duration of the analysis (600 s), in Hz. Each column represents recordings from a single biological replicate. Each dot represents recordings from a single electrode. ( E ) Example raw spikes from multi electrodes Array recording: 100 ms raw spikes of WT and Cdr1as-KO neurons DIV21. Each row represents one independent electrode (black bars).

    Article Snippet: Cells were seeded in 48-well CytoView MEA plates with 16 poly-3,4-ethylendioxythiophen (PEDOT) electrodes per well (Axion Biosystems).

    Techniques: Cell Culture, Activity Assay, Sampling, Selection