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16- or 24-channel linear electrode arrays with 50 μm interelectrode spacing v-probes  (plexon inc)

 
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    plexon inc 16- or 24-channel linear electrode arrays with 50 μm interelectrode spacing v-probes
    16 Or 24 Channel Linear Electrode Arrays With 50 μm Interelectrode Spacing V Probes, supplied by plexon inc, 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/linear+electrode+array/16++or+24++channel+laminar+v+probes/pmc10515157__pnas__2305759120__sapp-11-14-18
    Average 90 stars, based on 1 article reviews
    16- or 24-channel linear electrode arrays with 50 μm interelectrode spacing v-probes - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: Functional architecture of executive control and associated event-related potentials in macaques
    Article Snippet: Electroencephalogram (EEG) was recorded over the MFC with leads placed on the cranial surface beside the chamber while a linear electrode array (Plexon, 24 channels, 150 μm spacing) was inserted in SEF (Fig. ).

    Article Title: Visual Responses in FEF, Unlike V1, Primarily Reflect When the Visual Context Renders a Receptive Field Salient
    Article Snippet: In the second animal, a linear electrode array (“V-probe”, Plexon) was introduced transdurally in each recording session.

    Article Title: Model-based characterization of the selectivity of neurons in primary visual cortex.
    Article Snippet: In one animal, we implanted a 96-electrode planar Utah array (Blackrock Microsystems; 400 μm spacing), in the other, a linear electrode array (V-probe, Plexon; 24 contacts, 50μm spacing) was passed through the dura at the start of each day.

    Article Title: Model-based characterization of the selectivity of neurons in primary visual cortex
    Article Snippet: In one animal, we implanted a 96-electrode planar Utah array (Blackrock Microsystems; 400 mm spacing), in the other, a linear electrode array (V-probe, Plexon; 24 contacts, 50 μm spacing) was passed through the dura at the start of each day.

    Article Title: Functional Architecture of Executive Control and Associated Event-Related Potentials
    Article Snippet: 104 105 EEG was recorded with leads placed on the cranial surface beside the chamber over 106 medial frontal cortex while a linear electrode array (Plexon, 24 channels, 150 μm spacing) was 107 inserted in SEF (Fig. 1c).

    Activity Assay:

    Article Title: Working memory gates visual input to primate prefrontal neurons
    Article Snippet: Electrodes were lowered into the cortex using a hydraulic microdrive (Narishige). .. Neural activity was recorded extracellularly with varnish-coated tungsten microelectrodes (FHC) of 0.2–1.0 MΩ impedance (measured at 1 kHz) in V4, and via linear electrode array (v-probe, Plexon) in FEF. .. Extracellular waveforms were digitized and classified as single neurons using both template-matching and window discrimination techniques (FHC, Plexon).



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    SWA propagation axis are controlled by excitable populations in vivo (A) Schematic representation of the in vivo recording setup. (B) Representative example of the SWA activity recorded. Each color represents and individual shank, placed as shown in (A). Shaded traces were recorded in the cortex and used for further analysis. (C) Example of the detection of Up states, shown as faint red bars, based on the calculation of the log MUA of the recorded trace, shown in orange and blue respectively. (D) Relative delay of each shank along the Up states of one recordings session. Negative values are shown in the shanks on which the Up state was recorded first. Note how after NE + Cch are released, the more caudal shank (orange) shifts from positive to negative delays, while the contrary occurs for the rest of the shanks, as the wave becomes predominantly caudorostral. (E) Time lag matrix showing all the cortical electrodes and Up states recorded in a session. Note how following the release the caudal shank (orange) shifts from positive to negative delays, meaning that it becomes the first shank on which the Ups are detected. (F) Change in the ratio of rostrocaudal Up states following the release in all the recorded sessions. There is a significant ( p = 0.039) decrease in the amount of rostrocaudal Up states. Control recordings, on which saline was released as a substitute of the NE + CCh cocktail, do not show a significant change in the directionality of the SWA. p values calculated using Wilcoxon signed-rank test ( p value <0.05).

    Journal: iScience

    Article Title: Global and local nature of cortical slow waves

    doi: 10.1016/j.isci.2025.113213

    Figure Lengend Snippet: SWA propagation axis are controlled by excitable populations in vivo (A) Schematic representation of the in vivo recording setup. (B) Representative example of the SWA activity recorded. Each color represents and individual shank, placed as shown in (A). Shaded traces were recorded in the cortex and used for further analysis. (C) Example of the detection of Up states, shown as faint red bars, based on the calculation of the log MUA of the recorded trace, shown in orange and blue respectively. (D) Relative delay of each shank along the Up states of one recordings session. Negative values are shown in the shanks on which the Up state was recorded first. Note how after NE + Cch are released, the more caudal shank (orange) shifts from positive to negative delays, while the contrary occurs for the rest of the shanks, as the wave becomes predominantly caudorostral. (E) Time lag matrix showing all the cortical electrodes and Up states recorded in a session. Note how following the release the caudal shank (orange) shifts from positive to negative delays, meaning that it becomes the first shank on which the Ups are detected. (F) Change in the ratio of rostrocaudal Up states following the release in all the recorded sessions. There is a significant ( p = 0.039) decrease in the amount of rostrocaudal Up states. Control recordings, on which saline was released as a substitute of the NE + CCh cocktail, do not show a significant change in the directionality of the SWA. p values calculated using Wilcoxon signed-rank test ( p value <0.05).

    Article Snippet: One-third of the original induction dose was injected intramuscularly to maintain anesthesia once paw reflex could be evoked or the LFP trace exhibited signs of awakening, approximately every 2 h. Extracellular activity was then recorded by two linear silicon probe electrodes (NeuroNexus Technologies, Ann Arbor, MI).

    Techniques: In Vivo, Activity Assay, Control, Saline