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unilateral bipolar stimulating electrode #ms303/1-b/spc twisted stainless steel  (PlasticsOne inc)

 
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    PlasticsOne inc unilateral bipolar stimulating electrode #ms303/1-b/spc twisted stainless steel
    Unilateral Bipolar Stimulating Electrode #Ms303/1 B/Spc Twisted Stainless Steel, supplied by PlasticsOne 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/twisted+bipolar+stimulating+electrode/pm39836224-58-5-16?v=PlasticsOne+inc
    Average 90 stars, based on 1 article reviews
    unilateral bipolar stimulating electrode #ms303/1-b/spc twisted stainless steel - by Bioz Stars, 2026-06
    90/100 stars

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    PlasticsOne inc bipolar stimulation electrode 60-μm-diameter twisted stainless steel
    ( A ) Sketch of experimental setup for simultaneous patterned optogenetic <t>stimulation</t> and single-unit recording in AC and for intrinsic imaging. ( B ) AC window showing the location of a stimulation spot along the tonotopic axis of the primary auditory field (A1) with 64-channel silicon probe inserted via a hole in the coverglass (top right) to record single-unit responses to light patterns and illustrative data from three channels. ( C ) Responses of four AC neurons to different optogenetic stimulation patterns illustrating how spatiotemporal and spatial codes are extracted. ( D ) Sketch of the temporal modulation patterns applied to a single spot on the AC. ( E and F ) Z -scored responses of 344 single units to the 15 Hz high rate versus and 4 Hz high rate (E) and 15 Hz high rate versus 4 Hz low rate stimulations (F) ordered by preference for 15-Hz versus 4-Hz stimulation. Right: Difference in each neuron’s average firing rate between stimulations. ( G ) Accuracy of a neural decoder trained to discriminate between the optogenetic patterns based only on spatial information or with spatiotemporal information ( n = 344 units, bootstrap over units). ( H ) Sketch of the relative timing patterns applied to two spots A and B and the purely spatial pattern applied to either A or B. ( I and J ) Z -scored responses of 344 single units to A, B stimulations (I) and AB, BA stimulations (J), ordered by preference for A versus B stimulation. Right: Difference in each neuron’s average firing rate between stimulations. ( K ) Accuracy of a neural decoder trained to discriminate between the optogenetic patterns based only on spatial information or with spatiotemporal information ( n = 344 units, bootstrap over units).
    Bipolar Stimulation Electrode 60 μm Diameter Twisted Stainless Steel, supplied by PlasticsOne inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ( A ) Sketch of experimental setup for simultaneous patterned optogenetic <t>stimulation</t> and single-unit recording in AC and for intrinsic imaging. ( B ) AC window showing the location of a stimulation spot along the tonotopic axis of the primary auditory field (A1) with 64-channel silicon probe inserted via a hole in the coverglass (top right) to record single-unit responses to light patterns and illustrative data from three channels. ( C ) Responses of four AC neurons to different optogenetic stimulation patterns illustrating how spatiotemporal and spatial codes are extracted. ( D ) Sketch of the temporal modulation patterns applied to a single spot on the AC. ( E and F ) Z -scored responses of 344 single units to the 15 Hz high rate versus and 4 Hz high rate (E) and 15 Hz high rate versus 4 Hz low rate stimulations (F) ordered by preference for 15-Hz versus 4-Hz stimulation. Right: Difference in each neuron’s average firing rate between stimulations. ( G ) Accuracy of a neural decoder trained to discriminate between the optogenetic patterns based only on spatial information or with spatiotemporal information ( n = 344 units, bootstrap over units). ( H ) Sketch of the relative timing patterns applied to two spots A and B and the purely spatial pattern applied to either A or B. ( I and J ) Z -scored responses of 344 single units to A, B stimulations (I) and AB, BA stimulations (J), ordered by preference for A versus B stimulation. Right: Difference in each neuron’s average firing rate between stimulations. ( K ) Accuracy of a neural decoder trained to discriminate between the optogenetic patterns based only on spatial information or with spatiotemporal information ( n = 344 units, bootstrap over units).
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    PlasticsOne inc twisted-pair bipolar stimulating electrode (e363t/2/spc elec 0.008″/.2mm
    Experimental setup and fUSI recording protocol. (A) Schematic illustration of connectivity between the MSN and ROIs. Arrowheads represent axonal projections to and/or from MSN. (B) Experimental set-up showing the anesthetized mouse in a stereotaxic frame under the Iconeus One motorized probe mount. DBS <t>stimulating</t> electrodes were implanted on the left hemisphere and a sagittal plane of the right hemisphere was imaged. (C) Diagram of the protocol for the 60 min of continuous fUSI acquisition. After 5 min, saline or 1.0 mg/kg MK-801 was injected. After a total of 45 min of either theta, gamma, or no stimulation was applied for 5 min followed by 10 more minutes of recording.
    Twisted Pair Bipolar Stimulating Electrode (E363t/2/Spc Elec 0.008″/.2mm, supplied by PlasticsOne inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Experimental setup and fUSI recording protocol. (A) Schematic illustration of connectivity between the MSN and ROIs. Arrowheads represent axonal projections to and/or from MSN. (B) Experimental set-up showing the anesthetized mouse in a stereotaxic frame under the Iconeus One motorized probe mount. DBS <t>stimulating</t> electrodes were implanted on the left hemisphere and a sagittal plane of the right hemisphere was imaged. (C) Diagram of the protocol for the 60 min of continuous fUSI acquisition. After 5 min, saline or 1.0 mg/kg MK-801 was injected. After a total of 45 min of either theta, gamma, or no stimulation was applied for 5 min followed by 10 more minutes of recording.
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    Experimental setup and fUSI recording protocol. (A) Schematic illustration of connectivity between the MSN and ROIs. Arrowheads represent axonal projections to and/or from MSN. (B) Experimental set-up showing the anesthetized mouse in a stereotaxic frame under the Iconeus One motorized probe mount. DBS <t>stimulating</t> electrodes were implanted on the left hemisphere and a sagittal plane of the right hemisphere was imaged. (C) Diagram of the protocol for the 60 min of continuous fUSI acquisition. After 5 min, saline or 1.0 mg/kg MK-801 was injected. After a total of 45 min of either theta, gamma, or no stimulation was applied for 5 min followed by 10 more minutes of recording.
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    PlasticsOne inc twisted bipolar stimulating electrode plastics one
    Experimental setup and fUSI recording protocol. (A) Schematic illustration of connectivity between the MSN and ROIs. Arrowheads represent axonal projections to and/or from MSN. (B) Experimental set-up showing the anesthetized mouse in a stereotaxic frame under the Iconeus One motorized probe mount. DBS <t>stimulating</t> electrodes were implanted on the left hemisphere and a sagittal plane of the right hemisphere was imaged. (C) Diagram of the protocol for the 60 min of continuous fUSI acquisition. After 5 min, saline or 1.0 mg/kg MK-801 was injected. After a total of 45 min of either theta, gamma, or no stimulation was applied for 5 min followed by 10 more minutes of recording.
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    Image Search Results


    ( A ) Sketch of experimental setup for simultaneous patterned optogenetic stimulation and single-unit recording in AC and for intrinsic imaging. ( B ) AC window showing the location of a stimulation spot along the tonotopic axis of the primary auditory field (A1) with 64-channel silicon probe inserted via a hole in the coverglass (top right) to record single-unit responses to light patterns and illustrative data from three channels. ( C ) Responses of four AC neurons to different optogenetic stimulation patterns illustrating how spatiotemporal and spatial codes are extracted. ( D ) Sketch of the temporal modulation patterns applied to a single spot on the AC. ( E and F ) Z -scored responses of 344 single units to the 15 Hz high rate versus and 4 Hz high rate (E) and 15 Hz high rate versus 4 Hz low rate stimulations (F) ordered by preference for 15-Hz versus 4-Hz stimulation. Right: Difference in each neuron’s average firing rate between stimulations. ( G ) Accuracy of a neural decoder trained to discriminate between the optogenetic patterns based only on spatial information or with spatiotemporal information ( n = 344 units, bootstrap over units). ( H ) Sketch of the relative timing patterns applied to two spots A and B and the purely spatial pattern applied to either A or B. ( I and J ) Z -scored responses of 344 single units to A, B stimulations (I) and AB, BA stimulations (J), ordered by preference for A versus B stimulation. Right: Difference in each neuron’s average firing rate between stimulations. ( K ) Accuracy of a neural decoder trained to discriminate between the optogenetic patterns based only on spatial information or with spatiotemporal information ( n = 344 units, bootstrap over units).

    Journal: Science Advances

    Article Title: A spatial code for temporal information is necessary for efficient sensory learning

    doi: 10.1126/sciadv.adr6214

    Figure Lengend Snippet: ( A ) Sketch of experimental setup for simultaneous patterned optogenetic stimulation and single-unit recording in AC and for intrinsic imaging. ( B ) AC window showing the location of a stimulation spot along the tonotopic axis of the primary auditory field (A1) with 64-channel silicon probe inserted via a hole in the coverglass (top right) to record single-unit responses to light patterns and illustrative data from three channels. ( C ) Responses of four AC neurons to different optogenetic stimulation patterns illustrating how spatiotemporal and spatial codes are extracted. ( D ) Sketch of the temporal modulation patterns applied to a single spot on the AC. ( E and F ) Z -scored responses of 344 single units to the 15 Hz high rate versus and 4 Hz high rate (E) and 15 Hz high rate versus 4 Hz low rate stimulations (F) ordered by preference for 15-Hz versus 4-Hz stimulation. Right: Difference in each neuron’s average firing rate between stimulations. ( G ) Accuracy of a neural decoder trained to discriminate between the optogenetic patterns based only on spatial information or with spatiotemporal information ( n = 344 units, bootstrap over units). ( H ) Sketch of the relative timing patterns applied to two spots A and B and the purely spatial pattern applied to either A or B. ( I and J ) Z -scored responses of 344 single units to A, B stimulations (I) and AB, BA stimulations (J), ordered by preference for A versus B stimulation. Right: Difference in each neuron’s average firing rate between stimulations. ( K ) Accuracy of a neural decoder trained to discriminate between the optogenetic patterns based only on spatial information or with spatiotemporal information ( n = 344 units, bootstrap over units).

    Article Snippet: For MFB stimulation, a bipolar stimulation electrode (60-μm-diameter twisted stainless steel, PlasticsOne) was implanted using stereotaxic coordinates (antero-posterior−1.4, medio-lateral +1.2, dorso-ventral +4.8).

    Techniques: Single-unit Recording, Imaging

    ( A ) Sketch of experimental setup for behavioral discrimination of patterned optogenetic stimulation in AC and cranial window from an example mouse showing the location of the stimulation spots in the tonotopic axis of the primary auditory field. ( B ) Sample lick traces (top) and mean lick signal (bottom) for Go and NoGo trials in the task with temporal modulation and firing rate cues that the mouse successfully learnt (left) and in the task with temporal modulation cues only in which the mouse failed to discriminate (right). ( C ) Learning curves for an example mouse performing the two tasks with temporal modulation. ( D ) Learning curves for all mice performing the tasks with temporal modulation ( n = 7, error bars are SEM). ( E ) Accuracy at 2500 trials for all mice (paired Wilcoxon test, P = 0.031, signed rank value = 21, n = 6). ( F ) Learning curves for an example mouse performing the relative temporal order task and the spatial pattern task. ( G ) Learning curves for all mice performing each task ( n = 7, error bars are SEM). ( H ) Accuracy at 2500 trials for all mice (paired Wilcoxon test, P = 0.032, signed rank value = 27, n = 7).

    Journal: Science Advances

    Article Title: A spatial code for temporal information is necessary for efficient sensory learning

    doi: 10.1126/sciadv.adr6214

    Figure Lengend Snippet: ( A ) Sketch of experimental setup for behavioral discrimination of patterned optogenetic stimulation in AC and cranial window from an example mouse showing the location of the stimulation spots in the tonotopic axis of the primary auditory field. ( B ) Sample lick traces (top) and mean lick signal (bottom) for Go and NoGo trials in the task with temporal modulation and firing rate cues that the mouse successfully learnt (left) and in the task with temporal modulation cues only in which the mouse failed to discriminate (right). ( C ) Learning curves for an example mouse performing the two tasks with temporal modulation. ( D ) Learning curves for all mice performing the tasks with temporal modulation ( n = 7, error bars are SEM). ( E ) Accuracy at 2500 trials for all mice (paired Wilcoxon test, P = 0.031, signed rank value = 21, n = 6). ( F ) Learning curves for an example mouse performing the relative temporal order task and the spatial pattern task. ( G ) Learning curves for all mice performing each task ( n = 7, error bars are SEM). ( H ) Accuracy at 2500 trials for all mice (paired Wilcoxon test, P = 0.032, signed rank value = 27, n = 7).

    Article Snippet: For MFB stimulation, a bipolar stimulation electrode (60-μm-diameter twisted stainless steel, PlasticsOne) was implanted using stereotaxic coordinates (antero-posterior−1.4, medio-lateral +1.2, dorso-ventral +4.8).

    Techniques:

    Experimental setup and fUSI recording protocol. (A) Schematic illustration of connectivity between the MSN and ROIs. Arrowheads represent axonal projections to and/or from MSN. (B) Experimental set-up showing the anesthetized mouse in a stereotaxic frame under the Iconeus One motorized probe mount. DBS stimulating electrodes were implanted on the left hemisphere and a sagittal plane of the right hemisphere was imaged. (C) Diagram of the protocol for the 60 min of continuous fUSI acquisition. After 5 min, saline or 1.0 mg/kg MK-801 was injected. After a total of 45 min of either theta, gamma, or no stimulation was applied for 5 min followed by 10 more minutes of recording.

    Journal: Frontiers in Neuroscience

    Article Title: Theta-frequency medial septal nucleus deep brain stimulation increases neurovascular activity in MK-801-treated mice

    doi: 10.3389/fnins.2024.1372315

    Figure Lengend Snippet: Experimental setup and fUSI recording protocol. (A) Schematic illustration of connectivity between the MSN and ROIs. Arrowheads represent axonal projections to and/or from MSN. (B) Experimental set-up showing the anesthetized mouse in a stereotaxic frame under the Iconeus One motorized probe mount. DBS stimulating electrodes were implanted on the left hemisphere and a sagittal plane of the right hemisphere was imaged. (C) Diagram of the protocol for the 60 min of continuous fUSI acquisition. After 5 min, saline or 1.0 mg/kg MK-801 was injected. After a total of 45 min of either theta, gamma, or no stimulation was applied for 5 min followed by 10 more minutes of recording.

    Article Snippet: A 2 mm burr hole was then drilled to implant a twisted-pair bipolar stimulating electrode (E363T/2/SPC ELEC 0.008″/.2MM, Plastics One Inc., Roanoke, VA) targeting the midline MSN (AP: +0.7 mm, ML: −0.9 mm, from bregma.

    Techniques: Saline, Injection