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32 channel linear electrode  (NeuroNexus Technologies)


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    NeuroNexus Technologies 32 channel linear electrode
    32 Channel Linear Electrode, supplied by NeuroNexus Technologies, used in various techniques. Bioz Stars score: 97/100, based on 2516 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/linear+electrode+array/Silicon+Neural+Probe+%2F+Silicon+Microelectrode+Array/pm41366521-364-1-12
    Average 97 stars, based on 2516 article reviews
    32 channel linear electrode - by Bioz Stars, 2026-11
    97/100 stars

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    Related Articles

    Optogenetics:

    Article Title: Late UP-state bias in cortico-amygdalar coordination
    Article Snippet: .. 143 For acute mPFC recordings combined with optogenetic stimulation, a 32-channel silicon 144 probe with an integrated optical fiber (Buzsaki32-OA32LP-v2, NeuroNexus), coated with 145 DiO, was inserted into the mPFC (AP: 1.8 mm anterior to bregma; ML: 0.2 mm; DV: 1.5 146 mm). ..

    Silicon:

    Article Title: Late UP-state bias in cortico-amygdalar coordination
    Article Snippet: .. 143 For acute mPFC recordings combined with optogenetic stimulation, a 32-channel silicon 144 probe with an integrated optical fiber (Buzsaki32-OA32LP-v2, NeuroNexus), coated with 145 DiO, was inserted into the mPFC (AP: 1.8 mm anterior to bregma; ML: 0.2 mm; DV: 1.5 146 mm). ..

    Article Title: Navigational strategy dictates hippocampal representation of space in an everyday memory task
    Article Snippet: A craniotomy was made above the left hippocampus and an optic fiber (0.5 NA, core 400 μm SMA (FP400ERT, Thorlabs)) connected to a 625 nm fiber-coupled LED (M625F2, Thorlabs) was inserted above dorsal CA1 (AP 3.5, ML -2.6, DV -1.7). .. Next, a 32-channel 4-shank silicon probe (Buzsaki32, NeuroNexus) was inserted immediately posterior to the optic fiber, with shanks aligned with the proximo-distal axis of CA1. ..

    Article Title: Parallel retinal and circadian signalling channels organise mouse hypothalamic activity
    Article Snippet: Pupils were dilated by application of 1% atropine (Sigma Aldrich) BMC Biology and mineral oil applied to retain corneal moisture. .. Recordings used four shank silicon probes (Neuronexus), either with 32 channels (Buszaki32L, n = 6 mice) or 256 channels (4 × 64Poly2, four shanks spaced 200 μm each with two rows of 32 sites at 23 μm spacing; n = 14 mice). .. In either case, probes were coated in CM-DiI (V22888; Fisher Scientific, Loughborough, UK) for post hoc histological visualisation, prior to insertion into the brain to a depth of ~ 5.3 mm from the pial surface and an angle of 9° relative to the coronal plane.

    Article Title: A Reproducible Cortical Model of Focal Epileptiform Activity with a Multi-Biomarker Analysis Pipeline
    Article Snippet: Electrophysiological recordings were initially performed using tungsten stereotrodes during the development and optimization of the experimental model. Once the recording conditions and model parameters had been established, additional animals from each experimental group were recorded using 16-channel silicon probes (NeuroNexus Technologies, Inc., USA) to provide laminar recordings across the S1BF. .. Tungsten stereotrodes consisted of two twisted strands of 25 μm tungsten wire (Advent Research Materials, UK), whereas the 16-channel silicon probes (A1x16-5mm-50-177-A16; NeuroNexus) were connected through an Adpt-A16-OM32 adapter and comprised vertically aligned recording sites spaced 50 μm apart along a single shank, spanning a total distance of 750 μm ( ). ..

    Article Title: Representation of fear memory features in the ventral hippocampus.
    Article Snippet: .. Extracellular neuronal activity was recorded from right ventral CA1 hippocampus (-3.2mm posterior and +3.2mm lateral from the bregma and at a depth of 3.6 to 4.2 mm from brain surface) using silicon probes (NeuroNexus, 2 shank Takahashi probes with 2x32 channels and 4 shanks Buszaki probes with 8x4 channels). ..

    Tungsten:

    Article Title: A Reproducible Cortical Model of Focal Epileptiform Activity with a Multi-Biomarker Analysis Pipeline
    Article Snippet: Electrophysiological recordings were initially performed using tungsten stereotrodes during the development and optimization of the experimental model. Once the recording conditions and model parameters had been established, additional animals from each experimental group were recorded using 16-channel silicon probes (NeuroNexus Technologies, Inc., USA) to provide laminar recordings across the S1BF. .. Tungsten stereotrodes consisted of two twisted strands of 25 μm tungsten wire (Advent Research Materials, UK), whereas the 16-channel silicon probes (A1x16-5mm-50-177-A16; NeuroNexus) were connected through an Adpt-A16-OM32 adapter and comprised vertically aligned recording sites spaced 50 μm apart along a single shank, spanning a total distance of 750 μm ( ). ..

    Activity Assay:

    Article Title: Representation of fear memory features in the ventral hippocampus.
    Article Snippet: .. Extracellular neuronal activity was recorded from right ventral CA1 hippocampus (-3.2mm posterior and +3.2mm lateral from the bregma and at a depth of 3.6 to 4.2 mm from brain surface) using silicon probes (NeuroNexus, 2 shank Takahashi probes with 2x32 channels and 4 shanks Buszaki probes with 8x4 channels). ..



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    Image Search Results


    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