stimulating electrodes Search Results


94
ADInstruments stimulating bar electrode
Stimulating Bar Electrode, supplied by ADInstruments, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/stimulating+electrodes/Stimulating+Bar+Electrode/10__1109_slash_access__2020__3033075-144-1-6
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93
ADInstruments mla0320 nerve
Mla0320 Nerve, supplied by ADInstruments, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/stimulating+electrodes/Animal+Nerve+Stimulating+Electrode/pmc11033232-87-1-4
Average 93 stars, based on 1 article reviews
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93
ADInstruments platinum
Platinum, supplied by ADInstruments, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/stimulating+electrodes/Stimulating+Electrode+(platinum)+Length+Pole/pmc07178499-52-23-25
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92
ADInstruments stainless steel electrode
Stainless Steel Electrode, supplied by ADInstruments, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/stimulating+electrodes/Stimulating+Electrode+(stainless+steel)+Length+Pole/pm38990890-72-29-55
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90
BioSignal Group electrode system for electrical stimulation and biosignal detection
Electrode System For Electrical Stimulation And Biosignal Detection, supplied by BioSignal Group, 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/stimulating+electrodes/electrode+system+for+electrical+stimulation+and+biosignal+detection/us09981128-502-9-9
Average 90 stars, based on 1 article reviews
electrode system for electrical stimulation and biosignal detection - by Bioz Stars, 2026-10
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90
Ambu AS stimulating bar electrode
Stimulating Bar Electrode, supplied by Ambu AS, 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/stimulating+electrodes/stimulating+bar+electrode/pmc11727029-59-1-4
Average 90 stars, based on 1 article reviews
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90
BIOPAC bipolar subcutaneous needle stimulation electrode
Bipolar Subcutaneous Needle Stimulation Electrode, supplied by BIOPAC, 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/stimulating+electrodes/bipolar+subcutaneous+needle+stimulation+electrode/pm39844306-61-4-9
Average 90 stars, based on 1 article reviews
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Ambu AS electrostimulation electrode type neuroline 700
Electrostimulation Electrode Type Neuroline 700, supplied by Ambu AS, 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/stimulating+electrodes/surface+stimulation+electrodes+type+neuroline+700/pm35983754-72-5-14
Average 90 stars, based on 1 article reviews
electrostimulation electrode type neuroline 700 - by Bioz Stars, 2026-10
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90
BIOPAC stimulation electrodes
(a) 3D view of the rat head showing the coronal craniotomy (brown-shaded band) drilled between bregma −2.0 and −4.0 mm and extending 6.5 mm on each side from the sagittal suture for fUSi acquisition. The ultrasonic probe was positioned above the coronal craniotomy. This coronal plane was selected based on the Paxinos and Watson stereotaxic atlas32 in order to include the S1 barrel field, i.e. the <t>stimulation</t> target. A smaller round-shaped 1 mm2 craniotomy was performed at bregma +2.0 mm, lateral +7.0 mm to access the left MCA to place the microclip used for occlusion (black dot). Two pairs of stimulation <t>electrodes</t> (blue and red) were inserted in the whisker pads for stimulation of the unaffected and affected side, respectively. The stimulated area is shown in light gray shade. (b) Schematic representation of the experiment timelines. After baseline fUSi data acquisition (duration: 30 min which included the three runs of left and right whisker pad stimulation in the last 5 min), the left MCA was occluded (black arrowhead) for 90 min and the clip was then released (black arrowhead). Whisker pad stimulations (red and blue bars for left and right whisker pad stimulation, respectively) are depicted across the baseline, occlusion and reperfusion conditions. Each side was alternatively stimulated three times during the baseline period, and every 2 min throughout the occlusion and reperfusion periods. Interruptions in the stimulation bars represent the short time periods where the rat was removed from the experimental set-up to allow proceeding with MCAo and recanalization. Throughout the baseline, occlusion and reperfusion periods fUS images were acquired continuously every 0.7 s, except during the MCAo and reperfusion clip manipulations. After fUS imaging, rats were returned to their home cage for 48 h until perfusion-fixation for and immuno-histochemistry (see Methods) to assess infarction and selective neuronal loss (SNL); (c) Coronal fUSi image with superimposed “activated” pixels in response to whisker pad stimulation of the unaffected-side (left) whisker pad during baseline (image shown on the left), generated according to the voxel-based image processing procedures described in Methods. Activations are shown in % CBV increase compared to baseline (pseudo-colour scale on right of image). For illustration, similar images obtained during MCA occlusion and after reperfusion are also presented (middle and right, respectively), showing markedly increased contralesional rCBV responses to whisker stimulation in both conditions. Scale bar = 2.5 mm.
Stimulation Electrodes, supplied by BIOPAC, 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/stimulating+electrodes/stimulation+electrodes/pmc06168914-162-1-3
Average 90 stars, based on 1 article reviews
stimulation electrodes - by Bioz Stars, 2026-10
90/100 stars
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90
BIOPAC 2-mm shielded disc-stimulating electrode (model el2524s)
(a) 3D view of the rat head showing the coronal craniotomy (brown-shaded band) drilled between bregma −2.0 and −4.0 mm and extending 6.5 mm on each side from the sagittal suture for fUSi acquisition. The ultrasonic probe was positioned above the coronal craniotomy. This coronal plane was selected based on the Paxinos and Watson stereotaxic atlas32 in order to include the S1 barrel field, i.e. the <t>stimulation</t> target. A smaller round-shaped 1 mm2 craniotomy was performed at bregma +2.0 mm, lateral +7.0 mm to access the left MCA to place the microclip used for occlusion (black dot). Two pairs of stimulation <t>electrodes</t> (blue and red) were inserted in the whisker pads for stimulation of the unaffected and affected side, respectively. The stimulated area is shown in light gray shade. (b) Schematic representation of the experiment timelines. After baseline fUSi data acquisition (duration: 30 min which included the three runs of left and right whisker pad stimulation in the last 5 min), the left MCA was occluded (black arrowhead) for 90 min and the clip was then released (black arrowhead). Whisker pad stimulations (red and blue bars for left and right whisker pad stimulation, respectively) are depicted across the baseline, occlusion and reperfusion conditions. Each side was alternatively stimulated three times during the baseline period, and every 2 min throughout the occlusion and reperfusion periods. Interruptions in the stimulation bars represent the short time periods where the rat was removed from the experimental set-up to allow proceeding with MCAo and recanalization. Throughout the baseline, occlusion and reperfusion periods fUS images were acquired continuously every 0.7 s, except during the MCAo and reperfusion clip manipulations. After fUS imaging, rats were returned to their home cage for 48 h until perfusion-fixation for and immuno-histochemistry (see Methods) to assess infarction and selective neuronal loss (SNL); (c) Coronal fUSi image with superimposed “activated” pixels in response to whisker pad stimulation of the unaffected-side (left) whisker pad during baseline (image shown on the left), generated according to the voxel-based image processing procedures described in Methods. Activations are shown in % CBV increase compared to baseline (pseudo-colour scale on right of image). For illustration, similar images obtained during MCA occlusion and after reperfusion are also presented (middle and right, respectively), showing markedly increased contralesional rCBV responses to whisker stimulation in both conditions. Scale bar = 2.5 mm.
2 Mm Shielded Disc Stimulating Electrode (Model El2524s), supplied by BIOPAC, 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/stimulating+electrodes/shielded+disc+stimulating+electrode/pmc07319745-129-5-8
Average 90 stars, based on 1 article reviews
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90
BIOPAC hstm01 superficial stimulation electrodes
(a) 3D view of the rat head showing the coronal craniotomy (brown-shaded band) drilled between bregma −2.0 and −4.0 mm and extending 6.5 mm on each side from the sagittal suture for fUSi acquisition. The ultrasonic probe was positioned above the coronal craniotomy. This coronal plane was selected based on the Paxinos and Watson stereotaxic atlas32 in order to include the S1 barrel field, i.e. the <t>stimulation</t> target. A smaller round-shaped 1 mm2 craniotomy was performed at bregma +2.0 mm, lateral +7.0 mm to access the left MCA to place the microclip used for occlusion (black dot). Two pairs of stimulation <t>electrodes</t> (blue and red) were inserted in the whisker pads for stimulation of the unaffected and affected side, respectively. The stimulated area is shown in light gray shade. (b) Schematic representation of the experiment timelines. After baseline fUSi data acquisition (duration: 30 min which included the three runs of left and right whisker pad stimulation in the last 5 min), the left MCA was occluded (black arrowhead) for 90 min and the clip was then released (black arrowhead). Whisker pad stimulations (red and blue bars for left and right whisker pad stimulation, respectively) are depicted across the baseline, occlusion and reperfusion conditions. Each side was alternatively stimulated three times during the baseline period, and every 2 min throughout the occlusion and reperfusion periods. Interruptions in the stimulation bars represent the short time periods where the rat was removed from the experimental set-up to allow proceeding with MCAo and recanalization. Throughout the baseline, occlusion and reperfusion periods fUS images were acquired continuously every 0.7 s, except during the MCAo and reperfusion clip manipulations. After fUS imaging, rats were returned to their home cage for 48 h until perfusion-fixation for and immuno-histochemistry (see Methods) to assess infarction and selective neuronal loss (SNL); (c) Coronal fUSi image with superimposed “activated” pixels in response to whisker pad stimulation of the unaffected-side (left) whisker pad during baseline (image shown on the left), generated according to the voxel-based image processing procedures described in Methods. Activations are shown in % CBV increase compared to baseline (pseudo-colour scale on right of image). For illustration, similar images obtained during MCA occlusion and after reperfusion are also presented (middle and right, respectively), showing markedly increased contralesional rCBV responses to whisker stimulation in both conditions. Scale bar = 2.5 mm.
Hstm01 Superficial Stimulation Electrodes, supplied by BIOPAC, 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/stimulating+electrodes/hstm01+superficial+stimulation+electrodes/pmc04894235-60-50-54
Average 90 stars, based on 1 article reviews
hstm01 superficial stimulation electrodes - by Bioz Stars, 2026-10
90/100 stars
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90
CONMED Inc stimulating electrodes
(a) 3D view of the rat head showing the coronal craniotomy (brown-shaded band) drilled between bregma −2.0 and −4.0 mm and extending 6.5 mm on each side from the sagittal suture for fUSi acquisition. The ultrasonic probe was positioned above the coronal craniotomy. This coronal plane was selected based on the Paxinos and Watson stereotaxic atlas32 in order to include the S1 barrel field, i.e. the <t>stimulation</t> target. A smaller round-shaped 1 mm2 craniotomy was performed at bregma +2.0 mm, lateral +7.0 mm to access the left MCA to place the microclip used for occlusion (black dot). Two pairs of stimulation <t>electrodes</t> (blue and red) were inserted in the whisker pads for stimulation of the unaffected and affected side, respectively. The stimulated area is shown in light gray shade. (b) Schematic representation of the experiment timelines. After baseline fUSi data acquisition (duration: 30 min which included the three runs of left and right whisker pad stimulation in the last 5 min), the left MCA was occluded (black arrowhead) for 90 min and the clip was then released (black arrowhead). Whisker pad stimulations (red and blue bars for left and right whisker pad stimulation, respectively) are depicted across the baseline, occlusion and reperfusion conditions. Each side was alternatively stimulated three times during the baseline period, and every 2 min throughout the occlusion and reperfusion periods. Interruptions in the stimulation bars represent the short time periods where the rat was removed from the experimental set-up to allow proceeding with MCAo and recanalization. Throughout the baseline, occlusion and reperfusion periods fUS images were acquired continuously every 0.7 s, except during the MCAo and reperfusion clip manipulations. After fUS imaging, rats were returned to their home cage for 48 h until perfusion-fixation for and immuno-histochemistry (see Methods) to assess infarction and selective neuronal loss (SNL); (c) Coronal fUSi image with superimposed “activated” pixels in response to whisker pad stimulation of the unaffected-side (left) whisker pad during baseline (image shown on the left), generated according to the voxel-based image processing procedures described in Methods. Activations are shown in % CBV increase compared to baseline (pseudo-colour scale on right of image). For illustration, similar images obtained during MCA occlusion and after reperfusion are also presented (middle and right, respectively), showing markedly increased contralesional rCBV responses to whisker stimulation in both conditions. Scale bar = 2.5 mm.
Stimulating Electrodes, supplied by CONMED 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/stimulating+electrodes/stimulating+electrodes/pmc04060310-87-47-52
Average 90 stars, based on 1 article reviews
stimulating electrodes - by Bioz Stars, 2026-10
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Image Search Results


(a) 3D view of the rat head showing the coronal craniotomy (brown-shaded band) drilled between bregma −2.0 and −4.0 mm and extending 6.5 mm on each side from the sagittal suture for fUSi acquisition. The ultrasonic probe was positioned above the coronal craniotomy. This coronal plane was selected based on the Paxinos and Watson stereotaxic atlas32 in order to include the S1 barrel field, i.e. the stimulation target. A smaller round-shaped 1 mm2 craniotomy was performed at bregma +2.0 mm, lateral +7.0 mm to access the left MCA to place the microclip used for occlusion (black dot). Two pairs of stimulation electrodes (blue and red) were inserted in the whisker pads for stimulation of the unaffected and affected side, respectively. The stimulated area is shown in light gray shade. (b) Schematic representation of the experiment timelines. After baseline fUSi data acquisition (duration: 30 min which included the three runs of left and right whisker pad stimulation in the last 5 min), the left MCA was occluded (black arrowhead) for 90 min and the clip was then released (black arrowhead). Whisker pad stimulations (red and blue bars for left and right whisker pad stimulation, respectively) are depicted across the baseline, occlusion and reperfusion conditions. Each side was alternatively stimulated three times during the baseline period, and every 2 min throughout the occlusion and reperfusion periods. Interruptions in the stimulation bars represent the short time periods where the rat was removed from the experimental set-up to allow proceeding with MCAo and recanalization. Throughout the baseline, occlusion and reperfusion periods fUS images were acquired continuously every 0.7 s, except during the MCAo and reperfusion clip manipulations. After fUS imaging, rats were returned to their home cage for 48 h until perfusion-fixation for and immuno-histochemistry (see Methods) to assess infarction and selective neuronal loss (SNL); (c) Coronal fUSi image with superimposed “activated” pixels in response to whisker pad stimulation of the unaffected-side (left) whisker pad during baseline (image shown on the left), generated according to the voxel-based image processing procedures described in Methods. Activations are shown in % CBV increase compared to baseline (pseudo-colour scale on right of image). For illustration, similar images obtained during MCA occlusion and after reperfusion are also presented (middle and right, respectively), showing markedly increased contralesional rCBV responses to whisker stimulation in both conditions. Scale bar = 2.5 mm.

Journal: Journal of Cerebral Blood Flow & Metabolism

Article Title: Evidence from functional ultrasound imaging of enhanced contralesional microvascular response to somatosensory stimulation in acute middle cerebral artery occlusion/reperfusion in rats: A marker of ultra-early network reorganization?

doi: 10.1177/0271678X18786359

Figure Lengend Snippet: (a) 3D view of the rat head showing the coronal craniotomy (brown-shaded band) drilled between bregma −2.0 and −4.0 mm and extending 6.5 mm on each side from the sagittal suture for fUSi acquisition. The ultrasonic probe was positioned above the coronal craniotomy. This coronal plane was selected based on the Paxinos and Watson stereotaxic atlas32 in order to include the S1 barrel field, i.e. the stimulation target. A smaller round-shaped 1 mm2 craniotomy was performed at bregma +2.0 mm, lateral +7.0 mm to access the left MCA to place the microclip used for occlusion (black dot). Two pairs of stimulation electrodes (blue and red) were inserted in the whisker pads for stimulation of the unaffected and affected side, respectively. The stimulated area is shown in light gray shade. (b) Schematic representation of the experiment timelines. After baseline fUSi data acquisition (duration: 30 min which included the three runs of left and right whisker pad stimulation in the last 5 min), the left MCA was occluded (black arrowhead) for 90 min and the clip was then released (black arrowhead). Whisker pad stimulations (red and blue bars for left and right whisker pad stimulation, respectively) are depicted across the baseline, occlusion and reperfusion conditions. Each side was alternatively stimulated three times during the baseline period, and every 2 min throughout the occlusion and reperfusion periods. Interruptions in the stimulation bars represent the short time periods where the rat was removed from the experimental set-up to allow proceeding with MCAo and recanalization. Throughout the baseline, occlusion and reperfusion periods fUS images were acquired continuously every 0.7 s, except during the MCAo and reperfusion clip manipulations. After fUS imaging, rats were returned to their home cage for 48 h until perfusion-fixation for and immuno-histochemistry (see Methods) to assess infarction and selective neuronal loss (SNL); (c) Coronal fUSi image with superimposed “activated” pixels in response to whisker pad stimulation of the unaffected-side (left) whisker pad during baseline (image shown on the left), generated according to the voxel-based image processing procedures described in Methods. Activations are shown in % CBV increase compared to baseline (pseudo-colour scale on right of image). For illustration, similar images obtained during MCA occlusion and after reperfusion are also presented (middle and right, respectively), showing markedly increased contralesional rCBV responses to whisker stimulation in both conditions. Scale bar = 2.5 mm.

Article Snippet: Two stimulation electrodes (Biopac Systems, Inc., USA) were inserted in each whisker pad prior to imaging ( ).

Techniques: Whisker Assay, Imaging, Immunohistochemistry, Generated