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16 channel silicone linear array electrodes  (NeuroNexus Technologies)


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    Structured Review

    NeuroNexus Technologies 16 channel silicone linear array electrodes
    16 Channel Silicone Linear Array Electrodes, supplied by NeuroNexus Technologies, used in various techniques. Bioz Stars score: 97/100, based on 2508 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/pm41413076-85-10-24
    Average 97 stars, based on 2508 article reviews
    16 channel silicone linear array electrodes - by Bioz Stars, 2026-10
    97/100 stars

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    Related Articles

    other:

    Article Title: Channelrhodopsin variants for high-rate optogenetic neurostimulation at low light intensities.
    Article Snippet: Prior to the oABR recordings, aABRs were measured using near-field acoustic stimulation, centered 30 cm in front of the animal’s head with a loudspeaker (Scanspeak Ultrasound or Vifa; Avisoft Bioacoustics).

    Activity Assay:

    Article Title: Transplantation of Human IPSC-derived Microglia Ameliorates Neuropathology and Circuit Dysfunction in Progranulin-Deficient Mice
    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. .. MUA signals were amplified 10,000 times and band-pass filtered between 100 Hz and 6 kHz using the RZ5 system (Tucker-Davis Technologies,TDT, SCR_006495).

    Article Title: Dual role of spreading depolarization in an epileptic focus.
    Article Snippet: .. Intracortical LFP and multiple unit activity (MUA) were recorded using two linear multichannel silicon probes with iridium electrodes (413 μm2 surface area, 100 μm separation distance; NeuroNexus). ..

    Microscopy:

    Article Title: Channelrhodopsin variants for high-rate optogenetic neurostimulation at low light intensities.
    Article Snippet: Co., Ltd., Changchun, China Fast computer-controlled shutter Uniblitz LS6ZM2 VincentAssociates, Rochester, USA Opolette 355 tunable laser system Opotek Inc., Carlsbad, USA Diode-pumped solid-state laser (LBX-488-40-CSB; 488 nm 40mW,) Oxxius Coherent Inc Upright Olympus BX51WI microscope with a x40/0.8 LUMPLFLN40XW objective Olympus Andor zyla sCMOS camera Andor mCherry HC Filter Set mirror (F36-508 HC-Set mCherry) AHF - IDEX/Semrock EGFP HC Filter Set mirror (F36-528 HC-Set EGFP) AHF - IDEX/Semrock EPC10 USB HEKA patch clamp amplifier Harvard Bioscience Inc. FieldMaxII-TOP laser power meter Coherent Temperature controller SC20 and CL-200A Warner Instruments Falcon cell strainer (100 μm) Corning 352360 VT 1200 vibratome Leica Microsystems, Wetzlar, Germany Borosilicate glass capillaries with filament (GB150F, 0.86 × 1.50 × 80 mm) Science Products, 154 Hofheim, Germany Imaging spacer Grace BioLabs SecureSeal TM (GBL654008-100EA) Sigma-Aldrich Optical fiber (200-μm diameter, 0.39 NA) Thorlabs 473 nm laser (MLLFN-473100) Changchun New Industry Optoelectronics Reagent/resource Reference or source Identifier or catalog number 488 nm laser (LBX-488-100) Oxxius Coherent Inc Laser power meter (Solo-2; PM103USB; S140C). .. Gentec-EO and Thorlabs National Instrument data acquisition cards (NI PCI6229) National Instruments Soundproof chamber Industrial Acoustics Loudspeaker (Scanspeak Ultrasound; Vifa) Avisoft Bioacoustics 0.25-inch microphone (4039; 46BF-1) Brüel & Kjaer, GRAS Preamplifier (12AQ) GRAS 32-channel linear silicone probe (A1x32-6mm-50-177A32, 50-μm thickness) NeuroNexus Digital Lynx 4S recording system Neuralynx LED chips (C460TR2227S2100) Cree Confocal microscope SP8 Leica, Hamburg, Germany Micromanipulator (SM-10 compact) Luigs & Neumann LEICA CM3050 S Crysotat Leica Biosystems, Nussloch GmbH 2025 Automated immunostaining system - Discovery XT Roche Diagnostics GmbH, Mannheim, Germany) .. The pcDNA3.1(−) (Invitrogen, Carlsbad, USA) derivatives carrying the humanized DNA sequences of Chronos-EYFP (Stigeoclonium helveticum ChR, accession number: KF992040; Klapoetke et al, 2014), ChR2-EYFP (C-terminally truncated variant Chop2315 of ChR2 from Chlamydomonas reinhardtii, accession number: AF461397; Nagel et al, 2003), ChR2(F219Y)-EYFP (Mager et al, 2018), and CatCh-EYFP (ChR2 L132C; Kleinlogel et al, 2011) were generated previously (MPI of Biophysics).

    Immunostaining:

    Article Title: Channelrhodopsin variants for high-rate optogenetic neurostimulation at low light intensities.
    Article Snippet: Co., Ltd., Changchun, China Fast computer-controlled shutter Uniblitz LS6ZM2 VincentAssociates, Rochester, USA Opolette 355 tunable laser system Opotek Inc., Carlsbad, USA Diode-pumped solid-state laser (LBX-488-40-CSB; 488 nm 40mW,) Oxxius Coherent Inc Upright Olympus BX51WI microscope with a x40/0.8 LUMPLFLN40XW objective Olympus Andor zyla sCMOS camera Andor mCherry HC Filter Set mirror (F36-508 HC-Set mCherry) AHF - IDEX/Semrock EGFP HC Filter Set mirror (F36-528 HC-Set EGFP) AHF - IDEX/Semrock EPC10 USB HEKA patch clamp amplifier Harvard Bioscience Inc. FieldMaxII-TOP laser power meter Coherent Temperature controller SC20 and CL-200A Warner Instruments Falcon cell strainer (100 μm) Corning 352360 VT 1200 vibratome Leica Microsystems, Wetzlar, Germany Borosilicate glass capillaries with filament (GB150F, 0.86 × 1.50 × 80 mm) Science Products, 154 Hofheim, Germany Imaging spacer Grace BioLabs SecureSeal TM (GBL654008-100EA) Sigma-Aldrich Optical fiber (200-μm diameter, 0.39 NA) Thorlabs 473 nm laser (MLLFN-473100) Changchun New Industry Optoelectronics Reagent/resource Reference or source Identifier or catalog number 488 nm laser (LBX-488-100) Oxxius Coherent Inc Laser power meter (Solo-2; PM103USB; S140C). .. Gentec-EO and Thorlabs National Instrument data acquisition cards (NI PCI6229) National Instruments Soundproof chamber Industrial Acoustics Loudspeaker (Scanspeak Ultrasound; Vifa) Avisoft Bioacoustics 0.25-inch microphone (4039; 46BF-1) Brüel & Kjaer, GRAS Preamplifier (12AQ) GRAS 32-channel linear silicone probe (A1x32-6mm-50-177A32, 50-μm thickness) NeuroNexus Digital Lynx 4S recording system Neuralynx LED chips (C460TR2227S2100) Cree Confocal microscope SP8 Leica, Hamburg, Germany Micromanipulator (SM-10 compact) Luigs & Neumann LEICA CM3050 S Crysotat Leica Biosystems, Nussloch GmbH 2025 Automated immunostaining system - Discovery XT Roche Diagnostics GmbH, Mannheim, Germany) .. The pcDNA3.1(−) (Invitrogen, Carlsbad, USA) derivatives carrying the humanized DNA sequences of Chronos-EYFP (Stigeoclonium helveticum ChR, accession number: KF992040; Klapoetke et al, 2014), ChR2-EYFP (C-terminally truncated variant Chop2315 of ChR2 from Chlamydomonas reinhardtii, accession number: AF461397; Nagel et al, 2003), ChR2(F219Y)-EYFP (Mager et al, 2018), and CatCh-EYFP (ChR2 L132C; Kleinlogel et al, 2011) were generated previously (MPI of Biophysics).



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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 <t>electrodes</t> 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).
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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