2 mω tungsten microelectrode Search Results


tungsten microelectrode 1.1–1.5 mω  (MicroProbes for Life Science)
90
MicroProbes for Life Science tungsten microelectrode 1.1–1.5 mω
Tungsten Microelectrode 1.1–1.5 Mω, supplied by MicroProbes for Life Science, 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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tungsten microelectrodes 2–4 mu  (fhc inc)
90
fhc inc tungsten microelectrodes 2–4 mu
Tungsten Microelectrodes 2–4 Mu, supplied by fhc 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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epoxy-coated 1.1–1.5 mω tungsten microelectrodes  (MicroProbes for Life Science)
90
MicroProbes for Life Science epoxy-coated 1.1–1.5 mω tungsten microelectrodes
Epoxy Coated 1.1–1.5 Mω Tungsten Microelectrodes, supplied by MicroProbes for Life Science, 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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extracellular microelectrodes 2 to 7mω tungsten  (fhc inc)
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fhc inc extracellular microelectrodes 2 to 7mω tungsten
Extracellular Microelectrodes 2 To 7mω Tungsten, supplied by fhc 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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extracellular microelectrodes 2 to 7mω tungsten - by Bioz Stars, 2026-09
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tungsten microelectrodes 5-9 mω  (Haer Inc)
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Haer Inc tungsten microelectrodes 5-9 mω
Tungsten Microelectrodes 5 9 Mω, supplied by Haer 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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1.0 mω tungsten microelectrode  (Alpha-Omega Engineering)
90
Alpha-Omega Engineering 1.0 mω tungsten microelectrode
1.0 Mω Tungsten Microelectrode, supplied by Alpha-Omega Engineering, 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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1.0 mω tungsten microelectrode - by Bioz Stars, 2026-09
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tungsten microelectrode of 0.125 mm diameter and 1- to 5-mω impedance  (fhc inc)
90
fhc inc tungsten microelectrode of 0.125 mm diameter and 1- to 5-mω impedance
Tungsten Microelectrode Of 0.125 Mm Diameter And 1 To 5 Mω Impedance, supplied by fhc 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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optrode (optical fiber + tungsten microelectrode of 0.5–0.8 mω, with a core diameter 120 μm)  (Thomas RECORDING)
90
Thomas RECORDING optrode (optical fiber + tungsten microelectrode of 0.5–0.8 mω, with a core diameter 120 μm)
A-F Representative micrographs of triple immunostaining of Vglut2 (pseudo-color in red with Alexa Fluor 647), Vgat (green with Alexa Fluor 488), and orexin (pseudo-color in white Alexa Fluor 594) in lateral hypothalamus of control ( A-C ) and Firoc ( D-F ) mice revealed a significantly decreased number of Vglut2 puncta together with increased Vgat puncta onto orexin neurons ( n = 100 orexin neurons/mouse, 3 mice per group; *** p < 0.001; Mann Whitney U Test). B , E 3D representation of an orexin neuron (from the inset in A and D ) using Imaris software. C , F , Surface area of the same orexin neurons shown in B and E showing Vglut (red points) and Vgat spots (green points). G Percentage of Vglut2 spots in orexin neurons from each experimental group ( n = 100 orexin neurons/mouse, 3 mice per group, *** p < 0.001; Mann Whitney U Test). H Percentage of Vgat spots ( n = 100 orexin neurons/mouse, 3 mice per group; *** p < 0.001; Mann Whitney U Test). I Excitatory/ inhibitory ratio ( E / I) is significantly decreased in Firoc mice ( n = 100 orexin neurons/mouse, 3 mice per group); *** p < 0.001; Mann Whitney U Test. Scale bars in A and D : 100 μm, and in B , C , E and F : 15 μm. J A cartoon showing the intracranial localization of the electrode of stimulation in LPO (inhibitory inputs) and the <t>optrode</t> (optogenetic blue LED + Tungsten recording electrode) used to identify orexinergic cells in the LH/PeF area. K Unitary activity of orexinergic neurons in Or-ChR and Firoc-ChR animals. BLUE light pulses elicited 0.9 ± 0.22 spikes/50 ms in orexinergic neurons of Control-ChR mice, and 1.1 ± 0.19 spikes/50 ms in orexin neurons of Firoc-ChR mice ( n = 11, and n = 14, respectively). Thus, orexin neurons of Control-ChR and Firoc-ChR do not display differences in basal conditions ( p = 0.7299). However, after LPO stimulation (inhibitory inputs) and optogenetic activation, control-ChR mice show a 13% inhibition (0.78 ± 0.19 spikes/50 ms; p = 0.1135), whereas Firoc-ChR display a 31% inhibition (0.76 ± 0.12 spikes/50 ms; ** p < 0.01; sex balanced, Two-way RM ANOVA, Sidak’s Multiple comparison tests). Scale bars in A and D : 100 μm, and in B , C , E and F : 15 μm.
Optrode (Optical Fiber + Tungsten Microelectrode Of 0.5–0.8 Mω, With A Core Diameter 120 μm), supplied by Thomas RECORDING, 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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optrode (optical fiber + tungsten microelectrode of 0.5–0.8 mω, with a core diameter 120 μm) - by Bioz Stars, 2026-09
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2 to 10 microelectrodes, made of quartz-insulated, tungsten-platinum material  (Thomas RECORDING)
90
Thomas RECORDING 2 to 10 microelectrodes, made of quartz-insulated, tungsten-platinum material
A-F Representative micrographs of triple immunostaining of Vglut2 (pseudo-color in red with Alexa Fluor 647), Vgat (green with Alexa Fluor 488), and orexin (pseudo-color in white Alexa Fluor 594) in lateral hypothalamus of control ( A-C ) and Firoc ( D-F ) mice revealed a significantly decreased number of Vglut2 puncta together with increased Vgat puncta onto orexin neurons ( n = 100 orexin neurons/mouse, 3 mice per group; *** p < 0.001; Mann Whitney U Test). B , E 3D representation of an orexin neuron (from the inset in A and D ) using Imaris software. C , F , Surface area of the same orexin neurons shown in B and E showing Vglut (red points) and Vgat spots (green points). G Percentage of Vglut2 spots in orexin neurons from each experimental group ( n = 100 orexin neurons/mouse, 3 mice per group, *** p < 0.001; Mann Whitney U Test). H Percentage of Vgat spots ( n = 100 orexin neurons/mouse, 3 mice per group; *** p < 0.001; Mann Whitney U Test). I Excitatory/ inhibitory ratio ( E / I) is significantly decreased in Firoc mice ( n = 100 orexin neurons/mouse, 3 mice per group); *** p < 0.001; Mann Whitney U Test. Scale bars in A and D : 100 μm, and in B , C , E and F : 15 μm. J A cartoon showing the intracranial localization of the electrode of stimulation in LPO (inhibitory inputs) and the <t>optrode</t> (optogenetic blue LED + Tungsten recording electrode) used to identify orexinergic cells in the LH/PeF area. K Unitary activity of orexinergic neurons in Or-ChR and Firoc-ChR animals. BLUE light pulses elicited 0.9 ± 0.22 spikes/50 ms in orexinergic neurons of Control-ChR mice, and 1.1 ± 0.19 spikes/50 ms in orexin neurons of Firoc-ChR mice ( n = 11, and n = 14, respectively). Thus, orexin neurons of Control-ChR and Firoc-ChR do not display differences in basal conditions ( p = 0.7299). However, after LPO stimulation (inhibitory inputs) and optogenetic activation, control-ChR mice show a 13% inhibition (0.78 ± 0.19 spikes/50 ms; p = 0.1135), whereas Firoc-ChR display a 31% inhibition (0.76 ± 0.12 spikes/50 ms; ** p < 0.01; sex balanced, Two-way RM ANOVA, Sidak’s Multiple comparison tests). Scale bars in A and D : 100 μm, and in B , C , E and F : 15 μm.
2 To 10 Microelectrodes, Made Of Quartz Insulated, Tungsten Platinum Material, supplied by Thomas RECORDING, 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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2 to 10 microelectrodes, made of quartz-insulated, tungsten-platinum material - by Bioz Stars, 2026-09
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diameter lacquer-insulated tungsten microelectrode mng active/1 mω  (fhc inc)
90
fhc inc diameter lacquer-insulated tungsten microelectrode mng active/1 mω
A-F Representative micrographs of triple immunostaining of Vglut2 (pseudo-color in red with Alexa Fluor 647), Vgat (green with Alexa Fluor 488), and orexin (pseudo-color in white Alexa Fluor 594) in lateral hypothalamus of control ( A-C ) and Firoc ( D-F ) mice revealed a significantly decreased number of Vglut2 puncta together with increased Vgat puncta onto orexin neurons ( n = 100 orexin neurons/mouse, 3 mice per group; *** p < 0.001; Mann Whitney U Test). B , E 3D representation of an orexin neuron (from the inset in A and D ) using Imaris software. C , F , Surface area of the same orexin neurons shown in B and E showing Vglut (red points) and Vgat spots (green points). G Percentage of Vglut2 spots in orexin neurons from each experimental group ( n = 100 orexin neurons/mouse, 3 mice per group, *** p < 0.001; Mann Whitney U Test). H Percentage of Vgat spots ( n = 100 orexin neurons/mouse, 3 mice per group; *** p < 0.001; Mann Whitney U Test). I Excitatory/ inhibitory ratio ( E / I) is significantly decreased in Firoc mice ( n = 100 orexin neurons/mouse, 3 mice per group); *** p < 0.001; Mann Whitney U Test. Scale bars in A and D : 100 μm, and in B , C , E and F : 15 μm. J A cartoon showing the intracranial localization of the electrode of stimulation in LPO (inhibitory inputs) and the <t>optrode</t> (optogenetic blue LED + Tungsten recording electrode) used to identify orexinergic cells in the LH/PeF area. K Unitary activity of orexinergic neurons in Or-ChR and Firoc-ChR animals. BLUE light pulses elicited 0.9 ± 0.22 spikes/50 ms in orexinergic neurons of Control-ChR mice, and 1.1 ± 0.19 spikes/50 ms in orexin neurons of Firoc-ChR mice ( n = 11, and n = 14, respectively). Thus, orexin neurons of Control-ChR and Firoc-ChR do not display differences in basal conditions ( p = 0.7299). However, after LPO stimulation (inhibitory inputs) and optogenetic activation, control-ChR mice show a 13% inhibition (0.78 ± 0.19 spikes/50 ms; p = 0.1135), whereas Firoc-ChR display a 31% inhibition (0.76 ± 0.12 spikes/50 ms; ** p < 0.01; sex balanced, Two-way RM ANOVA, Sidak’s Multiple comparison tests). Scale bars in A and D : 100 μm, and in B , C , E and F : 15 μm.
Diameter Lacquer Insulated Tungsten Microelectrode Mng Active/1 Mω, supplied by fhc 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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diameter lacquer-insulated tungsten microelectrode mng active/1 mω - by Bioz Stars, 2026-09
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tungsten microelectrodes fhc 2–3 mω at 1 khz  (fhc inc)
90
fhc inc tungsten microelectrodes fhc 2–3 mω at 1 khz
A-F Representative micrographs of triple immunostaining of Vglut2 (pseudo-color in red with Alexa Fluor 647), Vgat (green with Alexa Fluor 488), and orexin (pseudo-color in white Alexa Fluor 594) in lateral hypothalamus of control ( A-C ) and Firoc ( D-F ) mice revealed a significantly decreased number of Vglut2 puncta together with increased Vgat puncta onto orexin neurons ( n = 100 orexin neurons/mouse, 3 mice per group; *** p < 0.001; Mann Whitney U Test). B , E 3D representation of an orexin neuron (from the inset in A and D ) using Imaris software. C , F , Surface area of the same orexin neurons shown in B and E showing Vglut (red points) and Vgat spots (green points). G Percentage of Vglut2 spots in orexin neurons from each experimental group ( n = 100 orexin neurons/mouse, 3 mice per group, *** p < 0.001; Mann Whitney U Test). H Percentage of Vgat spots ( n = 100 orexin neurons/mouse, 3 mice per group; *** p < 0.001; Mann Whitney U Test). I Excitatory/ inhibitory ratio ( E / I) is significantly decreased in Firoc mice ( n = 100 orexin neurons/mouse, 3 mice per group); *** p < 0.001; Mann Whitney U Test. Scale bars in A and D : 100 μm, and in B , C , E and F : 15 μm. J A cartoon showing the intracranial localization of the electrode of stimulation in LPO (inhibitory inputs) and the <t>optrode</t> (optogenetic blue LED + Tungsten recording electrode) used to identify orexinergic cells in the LH/PeF area. K Unitary activity of orexinergic neurons in Or-ChR and Firoc-ChR animals. BLUE light pulses elicited 0.9 ± 0.22 spikes/50 ms in orexinergic neurons of Control-ChR mice, and 1.1 ± 0.19 spikes/50 ms in orexin neurons of Firoc-ChR mice ( n = 11, and n = 14, respectively). Thus, orexin neurons of Control-ChR and Firoc-ChR do not display differences in basal conditions ( p = 0.7299). However, after LPO stimulation (inhibitory inputs) and optogenetic activation, control-ChR mice show a 13% inhibition (0.78 ± 0.19 spikes/50 ms; p = 0.1135), whereas Firoc-ChR display a 31% inhibition (0.76 ± 0.12 spikes/50 ms; ** p < 0.01; sex balanced, Two-way RM ANOVA, Sidak’s Multiple comparison tests). Scale bars in A and D : 100 μm, and in B , C , E and F : 15 μm.
Tungsten Microelectrodes Fhc 2–3 Mω At 1 Khz, supplied by fhc 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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tungsten microelectrodes (1–2 m)  (Marzhauser Wetzlar GmbH Co KG)
90
Marzhauser Wetzlar GmbH Co KG tungsten microelectrodes (1–2 m)
A-F Representative micrographs of triple immunostaining of Vglut2 (pseudo-color in red with Alexa Fluor 647), Vgat (green with Alexa Fluor 488), and orexin (pseudo-color in white Alexa Fluor 594) in lateral hypothalamus of control ( A-C ) and Firoc ( D-F ) mice revealed a significantly decreased number of Vglut2 puncta together with increased Vgat puncta onto orexin neurons ( n = 100 orexin neurons/mouse, 3 mice per group; *** p < 0.001; Mann Whitney U Test). B , E 3D representation of an orexin neuron (from the inset in A and D ) using Imaris software. C , F , Surface area of the same orexin neurons shown in B and E showing Vglut (red points) and Vgat spots (green points). G Percentage of Vglut2 spots in orexin neurons from each experimental group ( n = 100 orexin neurons/mouse, 3 mice per group, *** p < 0.001; Mann Whitney U Test). H Percentage of Vgat spots ( n = 100 orexin neurons/mouse, 3 mice per group; *** p < 0.001; Mann Whitney U Test). I Excitatory/ inhibitory ratio ( E / I) is significantly decreased in Firoc mice ( n = 100 orexin neurons/mouse, 3 mice per group); *** p < 0.001; Mann Whitney U Test. Scale bars in A and D : 100 μm, and in B , C , E and F : 15 μm. J A cartoon showing the intracranial localization of the electrode of stimulation in LPO (inhibitory inputs) and the <t>optrode</t> (optogenetic blue LED + Tungsten recording electrode) used to identify orexinergic cells in the LH/PeF area. K Unitary activity of orexinergic neurons in Or-ChR and Firoc-ChR animals. BLUE light pulses elicited 0.9 ± 0.22 spikes/50 ms in orexinergic neurons of Control-ChR mice, and 1.1 ± 0.19 spikes/50 ms in orexin neurons of Firoc-ChR mice ( n = 11, and n = 14, respectively). Thus, orexin neurons of Control-ChR and Firoc-ChR do not display differences in basal conditions ( p = 0.7299). However, after LPO stimulation (inhibitory inputs) and optogenetic activation, control-ChR mice show a 13% inhibition (0.78 ± 0.19 spikes/50 ms; p = 0.1135), whereas Firoc-ChR display a 31% inhibition (0.76 ± 0.12 spikes/50 ms; ** p < 0.01; sex balanced, Two-way RM ANOVA, Sidak’s Multiple comparison tests). Scale bars in A and D : 100 μm, and in B , C , E and F : 15 μm.
Tungsten Microelectrodes (1–2 M), supplied by Marzhauser Wetzlar GmbH Co KG, 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/2+m%CF%89+tungsten+microelectrode/tungsten+microelectrodes++1+2+m+/10__1523_slash_jneurosci__5271___08__2009-43-18-29
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tungsten microelectrodes (1–2 m) - by Bioz Stars, 2026-09
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Image Search Results


A-F Representative micrographs of triple immunostaining of Vglut2 (pseudo-color in red with Alexa Fluor 647), Vgat (green with Alexa Fluor 488), and orexin (pseudo-color in white Alexa Fluor 594) in lateral hypothalamus of control ( A-C ) and Firoc ( D-F ) mice revealed a significantly decreased number of Vglut2 puncta together with increased Vgat puncta onto orexin neurons ( n = 100 orexin neurons/mouse, 3 mice per group; *** p < 0.001; Mann Whitney U Test). B , E 3D representation of an orexin neuron (from the inset in A and D ) using Imaris software. C , F , Surface area of the same orexin neurons shown in B and E showing Vglut (red points) and Vgat spots (green points). G Percentage of Vglut2 spots in orexin neurons from each experimental group ( n = 100 orexin neurons/mouse, 3 mice per group, *** p < 0.001; Mann Whitney U Test). H Percentage of Vgat spots ( n = 100 orexin neurons/mouse, 3 mice per group; *** p < 0.001; Mann Whitney U Test). I Excitatory/ inhibitory ratio ( E / I) is significantly decreased in Firoc mice ( n = 100 orexin neurons/mouse, 3 mice per group); *** p < 0.001; Mann Whitney U Test. Scale bars in A and D : 100 μm, and in B , C , E and F : 15 μm. J A cartoon showing the intracranial localization of the electrode of stimulation in LPO (inhibitory inputs) and the optrode (optogenetic blue LED + Tungsten recording electrode) used to identify orexinergic cells in the LH/PeF area. K Unitary activity of orexinergic neurons in Or-ChR and Firoc-ChR animals. BLUE light pulses elicited 0.9 ± 0.22 spikes/50 ms in orexinergic neurons of Control-ChR mice, and 1.1 ± 0.19 spikes/50 ms in orexin neurons of Firoc-ChR mice ( n = 11, and n = 14, respectively). Thus, orexin neurons of Control-ChR and Firoc-ChR do not display differences in basal conditions ( p = 0.7299). However, after LPO stimulation (inhibitory inputs) and optogenetic activation, control-ChR mice show a 13% inhibition (0.78 ± 0.19 spikes/50 ms; p = 0.1135), whereas Firoc-ChR display a 31% inhibition (0.76 ± 0.12 spikes/50 ms; ** p < 0.01; sex balanced, Two-way RM ANOVA, Sidak’s Multiple comparison tests). Scale bars in A and D : 100 μm, and in B , C , E and F : 15 μm.

Journal: Molecular Psychiatry

Article Title: Insulin-like growth factor I mitigates post-traumatic stress by inhibiting AMP-kinase in orexin neurons

doi: 10.1038/s41380-022-01442-9

Figure Lengend Snippet: A-F Representative micrographs of triple immunostaining of Vglut2 (pseudo-color in red with Alexa Fluor 647), Vgat (green with Alexa Fluor 488), and orexin (pseudo-color in white Alexa Fluor 594) in lateral hypothalamus of control ( A-C ) and Firoc ( D-F ) mice revealed a significantly decreased number of Vglut2 puncta together with increased Vgat puncta onto orexin neurons ( n = 100 orexin neurons/mouse, 3 mice per group; *** p < 0.001; Mann Whitney U Test). B , E 3D representation of an orexin neuron (from the inset in A and D ) using Imaris software. C , F , Surface area of the same orexin neurons shown in B and E showing Vglut (red points) and Vgat spots (green points). G Percentage of Vglut2 spots in orexin neurons from each experimental group ( n = 100 orexin neurons/mouse, 3 mice per group, *** p < 0.001; Mann Whitney U Test). H Percentage of Vgat spots ( n = 100 orexin neurons/mouse, 3 mice per group; *** p < 0.001; Mann Whitney U Test). I Excitatory/ inhibitory ratio ( E / I) is significantly decreased in Firoc mice ( n = 100 orexin neurons/mouse, 3 mice per group); *** p < 0.001; Mann Whitney U Test. Scale bars in A and D : 100 μm, and in B , C , E and F : 15 μm. J A cartoon showing the intracranial localization of the electrode of stimulation in LPO (inhibitory inputs) and the optrode (optogenetic blue LED + Tungsten recording electrode) used to identify orexinergic cells in the LH/PeF area. K Unitary activity of orexinergic neurons in Or-ChR and Firoc-ChR animals. BLUE light pulses elicited 0.9 ± 0.22 spikes/50 ms in orexinergic neurons of Control-ChR mice, and 1.1 ± 0.19 spikes/50 ms in orexin neurons of Firoc-ChR mice ( n = 11, and n = 14, respectively). Thus, orexin neurons of Control-ChR and Firoc-ChR do not display differences in basal conditions ( p = 0.7299). However, after LPO stimulation (inhibitory inputs) and optogenetic activation, control-ChR mice show a 13% inhibition (0.78 ± 0.19 spikes/50 ms; p = 0.1135), whereas Firoc-ChR display a 31% inhibition (0.76 ± 0.12 spikes/50 ms; ** p < 0.01; sex balanced, Two-way RM ANOVA, Sidak’s Multiple comparison tests). Scale bars in A and D : 100 μm, and in B , C , E and F : 15 μm.

Article Snippet: An optrode (Optical fiber + Tungsten microelectrode of 0.5–0.8 MΩ, with a core diameter 120 μm; Thomas Recording) was used to record the evoked potential in the LH/PeF area (coordinates from Bregma: A,−1.95; L, 1.0 and depth, 4.0–4.5 mm).

Techniques: Triple Immunostaining, Control, MANN-WHITNEY, Software, Activity Assay, Activation Assay, Inhibition, Comparison