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borosilicate glass capillary recording electrode  (Sutter Instrument Company)


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    Structured Review

    Sutter Instrument Company borosilicate glass capillary recording electrode
    Borosilicate Glass Capillary Recording Electrode, supplied by Sutter Instrument Company, 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/result/borosilicate glass capillary recording electrode/product/Sutter Instrument Company
    Average 90 stars, based on 1 article reviews
    borosilicate glass capillary recording electrode - by Bioz Stars, 2026-03
    90/100 stars

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    Sutter Instrument Company recording electrodes borosilicate glass capillaries wpi #1b150f-4
    Morphine administration during the light cycle increases the number of spontaneously firing PVT neurons. A1 , ZT timeline showing times in which acute brain slices were prepared. Slices were prepared at either ZT2 (light) or ZT14 (dark). A2 , Coronal mouse brain slice showing an electrophysiological recording in the PVT (dashed shape outlines the recording <t>electrode</t> that is patched onto a PVT neuron). B , Representative traces showing the firing of PVT neurons 24 h following saline or morphine administration during light or dark cycles. C , Quantification of silent or spontaneously firing PVT neurons following repeated saline or morphine treatment. D , Summary showing the overall firing frequency of PVT neurons 24 h following repeated saline (Sal) or morphine (Mor) administration ( F (3,52) = 5.52, p = 0.002, one-way ANOVA); * p < 0.05. Scale bars: 40 mV, 2 s.
    Recording Electrodes Borosilicate Glass Capillaries Wpi #1b150f 4, supplied by Sutter Instrument Company, 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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    Morphine administration during the light cycle increases the number of spontaneously firing PVT neurons. A1 , ZT timeline showing times in which acute brain slices were prepared. Slices were prepared at either ZT2 (light) or ZT14 (dark). A2 , Coronal mouse brain slice showing an electrophysiological recording in the PVT (dashed shape outlines the recording electrode that is patched onto a PVT neuron). B , Representative traces showing the firing of PVT neurons 24 h following saline or morphine administration during light or dark cycles. C , Quantification of silent or spontaneously firing PVT neurons following repeated saline or morphine treatment. D , Summary showing the overall firing frequency of PVT neurons 24 h following repeated saline (Sal) or morphine (Mor) administration ( F (3,52) = 5.52, p = 0.002, one-way ANOVA); * p < 0.05. Scale bars: 40 mV, 2 s.

    Journal: eNeuro

    Article Title: Timing of Morphine Administration Differentially Alters Paraventricular Thalamic Neuron Activity

    doi: 10.1523/ENEURO.0377-19.2019

    Figure Lengend Snippet: Morphine administration during the light cycle increases the number of spontaneously firing PVT neurons. A1 , ZT timeline showing times in which acute brain slices were prepared. Slices were prepared at either ZT2 (light) or ZT14 (dark). A2 , Coronal mouse brain slice showing an electrophysiological recording in the PVT (dashed shape outlines the recording electrode that is patched onto a PVT neuron). B , Representative traces showing the firing of PVT neurons 24 h following saline or morphine administration during light or dark cycles. C , Quantification of silent or spontaneously firing PVT neurons following repeated saline or morphine treatment. D , Summary showing the overall firing frequency of PVT neurons 24 h following repeated saline (Sal) or morphine (Mor) administration ( F (3,52) = 5.52, p = 0.002, one-way ANOVA); * p < 0.05. Scale bars: 40 mV, 2 s.

    Article Snippet: For recordings of spontaneously firing neurons , recording electrodes [2–5 MΩ; borosilicate glass capillaries (WPI #1B150F-4) pulled on a horizontal puller from Sutter Instruments (model P-97)] were filled with a potassium-based internal solution containing the following: 130 mM KMeSO 3 , 10 mM KCl, 10 mM HEPES, 0.4 mM EGTA, 2 mM MgCl 2 -6H 2 0, 3 mM Mg-ATP, and 0.5 mM Na-GTP, pH 7.2–7.4.

    Techniques: Slice Preparation, Saline