epifluorescence microscope eclipse ni-e upright fluorescence microscope Search Results


epifluorescence microscope  (Nikon)
99
Nikon epifluorescence microscope
Epifluorescence Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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eclipse ni e epifluorescence microscope  (Nikon)
96
Nikon eclipse ni e epifluorescence microscope
Eclipse Ni E Epifluorescence Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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epifluorescence microscope eclipse ni e  (Nikon)
96
Nikon epifluorescence microscope eclipse ni e
Epifluorescence Microscope Eclipse Ni E, supplied by Nikon, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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lsm 510 meta confocal microscope  (Carl Zeiss)
90
Carl Zeiss lsm 510 meta confocal microscope
Lsm 510 Meta Confocal Microscope, supplied by Carl Zeiss, 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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a1 inverted eclipse ni e confocal microscopes  (Nikon)
99
Nikon a1 inverted eclipse ni e confocal microscopes
A1 Inverted Eclipse Ni E Confocal Microscopes, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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a1 inverted eclipse ni e confocal microscopes - by Bioz Stars, 2026-07
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upright nikon eclipse ni e fluorescence microscope  (Nikon)
99
Nikon upright nikon eclipse ni e fluorescence microscope
Upright Nikon Eclipse Ni E Fluorescence Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/epifluorescence+microscope+eclipse+ni-e+upright+fluorescence+microscope/varuzhanyan_grigor__2020__mitochondrial_dynamics_and_mitophagy_during_male_germline_development-954-8-9?v=Nikon
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lsm880  (Carl Zeiss)
90
Carl Zeiss lsm880
Lsm880, supplied by Carl Zeiss, 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/epifluorescence+microscope+eclipse+ni-e+upright+fluorescence+microscope/pm37599352-114-13-16?v=Carl+Zeiss
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epifluorescence microscope  (Olympus)
99
Olympus epifluorescence microscope
Anesthetics induce diverse modulation of Ca 2+ signals from individual GABAergic neurons in the vLPO. A) Schematic diagram depicting micro‐endoscopic recording of population Ca 2+ signal of GABAergic neurons in the vLPO. The GCaMP6‐expressing neurons were imaged using an <t>epifluorescence</t> <t>microscope</t> via an implanted GRIN lens. B) Representative field of view from an example imaging session. C) Example Ca 2+ signal (raw trace) from four simultaneously recorded neurons responding to the application of anesthetics. Each line is one neuron. The gray bar indicates the timing of the treatment. Scale bar, 10% ( ΔF / F 0 ) and 200 s. D) Statistical summary of the normalized modulation by each anesthetic. The normalized modulation index (NMI) was defined as the Ca 2+ signal (area under curve, AUC) after each treatment (10 min after each treatment, determined by DBI) minus the Ca 2+ signal during the baseline period (5 min before each treatment) divide by the sum of the two signals. Such that neurons inhibited by anesthetics will have a negative NMI, and the range of the NMI will be ≈ −1 to 1. The violin plots were a combination of kernel density plot (KDE) and box plot. The box plot shows a 25%∼75% range, the line shows a range within 1.5 IQR, and the dot represents the median. n = 359, 360, 303, and 375; p < 0.0001 for all comparison (Wilcoxon signed‐rank test). E) Heat map showing the Ca 2+ signal of each neuron during baseline and the period with an adequate level of anesthesia (determined using the DBI measurement). The recording periods were spliced together, and the white line indicates the splicing point (same for all heatmap plots in the following figures). Neurons were sorted by the NMI. F) Pie chart showing the percentage of neurons modulated by each anesthetic (up). Distribution of the NMI induced by each treatment (low).
Epifluorescence Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/epifluorescence+microscope+eclipse+ni-e+upright+fluorescence+microscope/pmc09839870-220-7-10?v=Olympus
Average 99 stars, based on 1 article reviews
epifluorescence microscope - by Bioz Stars, 2026-07
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zeiss lsm710  (Carl Zeiss)
90
Carl Zeiss zeiss lsm710
Anesthetics induce diverse modulation of Ca 2+ signals from individual GABAergic neurons in the vLPO. A) Schematic diagram depicting micro‐endoscopic recording of population Ca 2+ signal of GABAergic neurons in the vLPO. The GCaMP6‐expressing neurons were imaged using an <t>epifluorescence</t> <t>microscope</t> via an implanted GRIN lens. B) Representative field of view from an example imaging session. C) Example Ca 2+ signal (raw trace) from four simultaneously recorded neurons responding to the application of anesthetics. Each line is one neuron. The gray bar indicates the timing of the treatment. Scale bar, 10% ( ΔF / F 0 ) and 200 s. D) Statistical summary of the normalized modulation by each anesthetic. The normalized modulation index (NMI) was defined as the Ca 2+ signal (area under curve, AUC) after each treatment (10 min after each treatment, determined by DBI) minus the Ca 2+ signal during the baseline period (5 min before each treatment) divide by the sum of the two signals. Such that neurons inhibited by anesthetics will have a negative NMI, and the range of the NMI will be ≈ −1 to 1. The violin plots were a combination of kernel density plot (KDE) and box plot. The box plot shows a 25%∼75% range, the line shows a range within 1.5 IQR, and the dot represents the median. n = 359, 360, 303, and 375; p < 0.0001 for all comparison (Wilcoxon signed‐rank test). E) Heat map showing the Ca 2+ signal of each neuron during baseline and the period with an adequate level of anesthesia (determined using the DBI measurement). The recording periods were spliced together, and the white line indicates the splicing point (same for all heatmap plots in the following figures). Neurons were sorted by the NMI. F) Pie chart showing the percentage of neurons modulated by each anesthetic (up). Distribution of the NMI induced by each treatment (low).
Zeiss Lsm710, supplied by Carl Zeiss, 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/epifluorescence+microscope+eclipse+ni-e+upright+fluorescence+microscope/pmc04870516__mmc1-194-5-5?v=Carl+Zeiss
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microscope zeiss axio vert s100  (Carl Zeiss)
90
Carl Zeiss microscope zeiss axio vert s100
Anesthetics induce diverse modulation of Ca 2+ signals from individual GABAergic neurons in the vLPO. A) Schematic diagram depicting micro‐endoscopic recording of population Ca 2+ signal of GABAergic neurons in the vLPO. The GCaMP6‐expressing neurons were imaged using an <t>epifluorescence</t> <t>microscope</t> via an implanted GRIN lens. B) Representative field of view from an example imaging session. C) Example Ca 2+ signal (raw trace) from four simultaneously recorded neurons responding to the application of anesthetics. Each line is one neuron. The gray bar indicates the timing of the treatment. Scale bar, 10% ( ΔF / F 0 ) and 200 s. D) Statistical summary of the normalized modulation by each anesthetic. The normalized modulation index (NMI) was defined as the Ca 2+ signal (area under curve, AUC) after each treatment (10 min after each treatment, determined by DBI) minus the Ca 2+ signal during the baseline period (5 min before each treatment) divide by the sum of the two signals. Such that neurons inhibited by anesthetics will have a negative NMI, and the range of the NMI will be ≈ −1 to 1. The violin plots were a combination of kernel density plot (KDE) and box plot. The box plot shows a 25%∼75% range, the line shows a range within 1.5 IQR, and the dot represents the median. n = 359, 360, 303, and 375; p < 0.0001 for all comparison (Wilcoxon signed‐rank test). E) Heat map showing the Ca 2+ signal of each neuron during baseline and the period with an adequate level of anesthesia (determined using the DBI measurement). The recording periods were spliced together, and the white line indicates the splicing point (same for all heatmap plots in the following figures). Neurons were sorted by the NMI. F) Pie chart showing the percentage of neurons modulated by each anesthetic (up). Distribution of the NMI induced by each treatment (low).
Microscope Zeiss Axio Vert S100, supplied by Carl Zeiss, 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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microscope zeiss axio vert s100 - by Bioz Stars, 2026-07
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axiovert 200 m inverted microscope  (Carl Zeiss)
90
Carl Zeiss axiovert 200 m inverted microscope
Anesthetics induce diverse modulation of Ca 2+ signals from individual GABAergic neurons in the vLPO. A) Schematic diagram depicting micro‐endoscopic recording of population Ca 2+ signal of GABAergic neurons in the vLPO. The GCaMP6‐expressing neurons were imaged using an <t>epifluorescence</t> <t>microscope</t> via an implanted GRIN lens. B) Representative field of view from an example imaging session. C) Example Ca 2+ signal (raw trace) from four simultaneously recorded neurons responding to the application of anesthetics. Each line is one neuron. The gray bar indicates the timing of the treatment. Scale bar, 10% ( ΔF / F 0 ) and 200 s. D) Statistical summary of the normalized modulation by each anesthetic. The normalized modulation index (NMI) was defined as the Ca 2+ signal (area under curve, AUC) after each treatment (10 min after each treatment, determined by DBI) minus the Ca 2+ signal during the baseline period (5 min before each treatment) divide by the sum of the two signals. Such that neurons inhibited by anesthetics will have a negative NMI, and the range of the NMI will be ≈ −1 to 1. The violin plots were a combination of kernel density plot (KDE) and box plot. The box plot shows a 25%∼75% range, the line shows a range within 1.5 IQR, and the dot represents the median. n = 359, 360, 303, and 375; p < 0.0001 for all comparison (Wilcoxon signed‐rank test). E) Heat map showing the Ca 2+ signal of each neuron during baseline and the period with an adequate level of anesthesia (determined using the DBI measurement). The recording periods were spliced together, and the white line indicates the splicing point (same for all heatmap plots in the following figures). Neurons were sorted by the NMI. F) Pie chart showing the percentage of neurons modulated by each anesthetic (up). Distribution of the NMI induced by each treatment (low).
Axiovert 200 M Inverted Microscope, supplied by Carl Zeiss, 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/epifluorescence+microscope+eclipse+ni-e+upright+fluorescence+microscope/pm37485324-92-11-6?v=Carl+Zeiss
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Image Search Results


Anesthetics induce diverse modulation of Ca 2+ signals from individual GABAergic neurons in the vLPO. A) Schematic diagram depicting micro‐endoscopic recording of population Ca 2+ signal of GABAergic neurons in the vLPO. The GCaMP6‐expressing neurons were imaged using an epifluorescence microscope via an implanted GRIN lens. B) Representative field of view from an example imaging session. C) Example Ca 2+ signal (raw trace) from four simultaneously recorded neurons responding to the application of anesthetics. Each line is one neuron. The gray bar indicates the timing of the treatment. Scale bar, 10% ( ΔF / F 0 ) and 200 s. D) Statistical summary of the normalized modulation by each anesthetic. The normalized modulation index (NMI) was defined as the Ca 2+ signal (area under curve, AUC) after each treatment (10 min after each treatment, determined by DBI) minus the Ca 2+ signal during the baseline period (5 min before each treatment) divide by the sum of the two signals. Such that neurons inhibited by anesthetics will have a negative NMI, and the range of the NMI will be ≈ −1 to 1. The violin plots were a combination of kernel density plot (KDE) and box plot. The box plot shows a 25%∼75% range, the line shows a range within 1.5 IQR, and the dot represents the median. n = 359, 360, 303, and 375; p < 0.0001 for all comparison (Wilcoxon signed‐rank test). E) Heat map showing the Ca 2+ signal of each neuron during baseline and the period with an adequate level of anesthesia (determined using the DBI measurement). The recording periods were spliced together, and the white line indicates the splicing point (same for all heatmap plots in the following figures). Neurons were sorted by the NMI. F) Pie chart showing the percentage of neurons modulated by each anesthetic (up). Distribution of the NMI induced by each treatment (low).

Journal: Advanced Science

Article Title: Divergent Neural Activity in the VLPO During Anesthesia and Sleep

doi: 10.1002/advs.202203395

Figure Lengend Snippet: Anesthetics induce diverse modulation of Ca 2+ signals from individual GABAergic neurons in the vLPO. A) Schematic diagram depicting micro‐endoscopic recording of population Ca 2+ signal of GABAergic neurons in the vLPO. The GCaMP6‐expressing neurons were imaged using an epifluorescence microscope via an implanted GRIN lens. B) Representative field of view from an example imaging session. C) Example Ca 2+ signal (raw trace) from four simultaneously recorded neurons responding to the application of anesthetics. Each line is one neuron. The gray bar indicates the timing of the treatment. Scale bar, 10% ( ΔF / F 0 ) and 200 s. D) Statistical summary of the normalized modulation by each anesthetic. The normalized modulation index (NMI) was defined as the Ca 2+ signal (area under curve, AUC) after each treatment (10 min after each treatment, determined by DBI) minus the Ca 2+ signal during the baseline period (5 min before each treatment) divide by the sum of the two signals. Such that neurons inhibited by anesthetics will have a negative NMI, and the range of the NMI will be ≈ −1 to 1. The violin plots were a combination of kernel density plot (KDE) and box plot. The box plot shows a 25%∼75% range, the line shows a range within 1.5 IQR, and the dot represents the median. n = 359, 360, 303, and 375; p < 0.0001 for all comparison (Wilcoxon signed‐rank test). E) Heat map showing the Ca 2+ signal of each neuron during baseline and the period with an adequate level of anesthesia (determined using the DBI measurement). The recording periods were spliced together, and the white line indicates the splicing point (same for all heatmap plots in the following figures). Neurons were sorted by the NMI. F) Pie chart showing the percentage of neurons modulated by each anesthetic (up). Distribution of the NMI induced by each treatment (low).

Article Snippet: The fluorescence images were captured using an epifluorescence microscope (VS120, Olympus) or a confocal microscope (Eclipse Ni‐E or Ti‐E, Nikon).

Techniques: Expressing, Microscopy, Imaging, Comparison