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microelectrode array microprobe 2×8  (Blackrock Microsystems LLC)

 
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    Blackrock Microsystems LLC microelectrode array microprobe 2×8
    Microelectrode Array Microprobe 2×8, supplied by Blackrock Microsystems LLC, 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/multi-array+system/multi+electrode+arrays+and+acquisition+system/pmc03772573-85-7-27
    Average 90 stars, based on 1 article reviews
    microelectrode array microprobe 2×8 - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: Brain Function, Learning, and Role of Feedback in Complete Paralysis
    Article Snippet: Two 64 microelectrode arrays were implanted in the dominant left supplementary and primary motor cortex (8 × 8 electrodes each, 1.5 mm length, 0.4 mm electrode pitch; Blackrock Microsystems LLC).

    Article Title: Neural Dynamics in Primate Cortex during Exposure to Subanesthetic Concentrations of Nitrous Oxide
    Article Snippet: Two male rhesus macaques, Monkey W and Monkey N, were implanted with Utah Arrays with electrode lengths of 1.5 mm (Blackrock Microsystems) in M1 using methods previously described ( ).

    Article Title: Contributions of early and mid-level visual cortex to high-level object categorization
    Article Snippet: Simultaneous extracellular recordings using chronically implanted 6×8 microelectrode arrays (Blackrock Microsystems, arrays placed in one hemisphere) were obtained in monkey M1 (visual areas V1 and V4, one array in each area) and monkey M2 (visual area V4, data from one of two arrays implanted analyzed in this study).

    Article Title: Propagating motor cortical dynamics facilitate movement initiation
    Article Snippet: EXPERIMENTAL MODEL AND SUBJECT DETAILS Electrophysiology Three male Rhesus ( Macaca Mulatta ) monkeys (Bx, Ls, and Mk) were implanted with Utah multi-electrode arrays (1.5 electrode length for Bx; 1.0 mm electrode length for Ls and Mk and 400 μm pitch from Blackrock Microsystems, Inc. Salt Lake City, UT) in the upper limb region of primary motor cortex (M1), on the contralateral side of the active limb used in the task.

    Article Title: Chronic wireless neural population recordings with common marmosets
    Article Snippet: DECLARATION OF INTERESTS N.G.H. serves as a consultant for BlackRock Microsystems, Inc., the company that sells the multi-electrode arrays and acquisition system used in this study.

    Article Title: Conveying tactile object characteristics through customized intracortical microstimulation of the human somatosensory cortex
    Article Snippet: Prior to this study, participants were implanted with two 2.4 x 4 mm microelectrode arrays (Blackrock Microsystems, Salt Lake City, UT) in Brodmann area 1 in their left hemisphere , , .

    Article Title: Contributions of early and mid-level visual cortex to high-level object categorization
    Article Snippet: Simultaneous extracellular recordings using chronically implanted 6x8 microelectrode arrays (Blackrock Microsystems, arrays placed in one hemisphere) were obtained in monkey M1 (visual areas V1 and V4, one array in each area) and monkey M2 (visual area V4, data from one of two arrays implanted analyzed in this study).



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    (A) Representative image of multi-unit recordings setup of ex vivo thalamic horizontal slices in a humidified, oxygenated interface chamber. (B) Schematic of multi-unit activity recordings with a <t>Neuronexus</t> <t>16-channel</t> recording electrode positioned in the thalamus following electrical stimulation of the internal capsule. (C) Representative 3-second recording of intrathalamic multi-unit activity evoked by stimulation of the internal capsule (black dot indicates time of stimulation). Only 12 of 16 channels are shown for clarity. (D) Collapsed activity from 12 recording channels in (C). Black dot indicates time of stimulation. (E) Post-stimulus time histogram of instantaneous spiking frequency from multi-unit activity recorded across 16 channels (all 16 channels were analyzed, 12 representative channels are displayed in (C) from 15 slices from 9 hCSF1 (WT) mice, 8 slices from 7 hCSF1-Grn −/− +KOxMG mice, and 12 slices from 9 hCSF1-Grn −/− +WTxMG mice. The grey box denotes early response (0–1.5 s), and the white box denotes delayed response (1.5–3 s) after stimulation. (F) Enlarged instantaneous frequency of the delayed response (1.5–3 s) from (D). (G) Relative probability of eliciting spiking during the direct response (0–1.5 s) after stimulation; p values from Kolmogorov-Smirnov test with Bonferroni correction (* p = 0.0024). (H) Instantaneous frequency of spiking during the early response (0–1.5 s) after stimulation; Kruskal–Wallis test, H(3) = 6.767, p = 0.0797. (I) Relative probability of eliciting spiking during the delayed response (1.5–3 s) after stimulation; p values from Kolmogorov-Smirnov test with Bonferroni correction (**** p < 0.0001). (J) Instantaneous frequency of spiking during the delayed response (1.5–3 s) after stimulation; Kruskal-Wallis test, H(3)=56.6, **** p < 0.0001, and Dunn’s multiple comparisons test (**** p < 0.0001). Data are presented as mean ± SEM. Comparisons not shown are not significant.
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    Image Search Results


    (A) Representative image of multi-unit recordings setup of ex vivo thalamic horizontal slices in a humidified, oxygenated interface chamber. (B) Schematic of multi-unit activity recordings with a Neuronexus 16-channel recording electrode positioned in the thalamus following electrical stimulation of the internal capsule. (C) Representative 3-second recording of intrathalamic multi-unit activity evoked by stimulation of the internal capsule (black dot indicates time of stimulation). Only 12 of 16 channels are shown for clarity. (D) Collapsed activity from 12 recording channels in (C). Black dot indicates time of stimulation. (E) Post-stimulus time histogram of instantaneous spiking frequency from multi-unit activity recorded across 16 channels (all 16 channels were analyzed, 12 representative channels are displayed in (C) from 15 slices from 9 hCSF1 (WT) mice, 8 slices from 7 hCSF1-Grn −/− +KOxMG mice, and 12 slices from 9 hCSF1-Grn −/− +WTxMG mice. The grey box denotes early response (0–1.5 s), and the white box denotes delayed response (1.5–3 s) after stimulation. (F) Enlarged instantaneous frequency of the delayed response (1.5–3 s) from (D). (G) Relative probability of eliciting spiking during the direct response (0–1.5 s) after stimulation; p values from Kolmogorov-Smirnov test with Bonferroni correction (* p = 0.0024). (H) Instantaneous frequency of spiking during the early response (0–1.5 s) after stimulation; Kruskal–Wallis test, H(3) = 6.767, p = 0.0797. (I) Relative probability of eliciting spiking during the delayed response (1.5–3 s) after stimulation; p values from Kolmogorov-Smirnov test with Bonferroni correction (**** p < 0.0001). (J) Instantaneous frequency of spiking during the delayed response (1.5–3 s) after stimulation; Kruskal-Wallis test, H(3)=56.6, **** p < 0.0001, and Dunn’s multiple comparisons test (**** p < 0.0001). Data are presented as mean ± SEM. Comparisons not shown are not significant.

    Journal: bioRxiv

    Article Title: Transplantation of Human IPSC-derived Microglia Ameliorates Neuropathology and Circuit Dysfunction in Progranulin-Deficient Mice

    doi: 10.64898/2026.01.13.699312

    Figure Lengend Snippet: (A) Representative image of multi-unit recordings setup of ex vivo thalamic horizontal slices in a humidified, oxygenated interface chamber. (B) Schematic of multi-unit activity recordings with a Neuronexus 16-channel recording electrode positioned in the thalamus following electrical stimulation of the internal capsule. (C) Representative 3-second recording of intrathalamic multi-unit activity evoked by stimulation of the internal capsule (black dot indicates time of stimulation). Only 12 of 16 channels are shown for clarity. (D) Collapsed activity from 12 recording channels in (C). Black dot indicates time of stimulation. (E) Post-stimulus time histogram of instantaneous spiking frequency from multi-unit activity recorded across 16 channels (all 16 channels were analyzed, 12 representative channels are displayed in (C) from 15 slices from 9 hCSF1 (WT) mice, 8 slices from 7 hCSF1-Grn −/− +KOxMG mice, and 12 slices from 9 hCSF1-Grn −/− +WTxMG mice. The grey box denotes early response (0–1.5 s), and the white box denotes delayed response (1.5–3 s) after stimulation. (F) Enlarged instantaneous frequency of the delayed response (1.5–3 s) from (D). (G) Relative probability of eliciting spiking during the direct response (0–1.5 s) after stimulation; p values from Kolmogorov-Smirnov test with Bonferroni correction (* p = 0.0024). (H) Instantaneous frequency of spiking during the early response (0–1.5 s) after stimulation; Kruskal–Wallis test, H(3) = 6.767, p = 0.0797. (I) Relative probability of eliciting spiking during the delayed response (1.5–3 s) after stimulation; p values from Kolmogorov-Smirnov test with Bonferroni correction (**** p < 0.0001). (J) Instantaneous frequency of spiking during the delayed response (1.5–3 s) after stimulation; Kruskal-Wallis test, H(3)=56.6, **** p < 0.0001, and Dunn’s multiple comparisons test (**** p < 0.0001). Data are presented as mean ± SEM. Comparisons not shown are not significant.

    Article Snippet: Extracellular multi-unit activity (MUA) recordings were obtained with a linear 16-channel multi-electrode array (Neuronexus) that spanned the nRT and VB thalamic regions.

    Techniques: Ex Vivo, Activity Assay