confocal fluorescent microscope n-storm superresolution Search Results


interferometric fluorescent superresolution microscopy  (Galbraith Laboratories Inc)
86
Galbraith Laboratories Inc interferometric fluorescent superresolution microscopy
Interferometric Fluorescent Superresolution Microscopy, supplied by Galbraith Laboratories Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ni eclipse inverted microscope  (Nikon)
99
Nikon ni eclipse inverted microscope
Figure 4. (A) Super-resolution light microscopy image of somatostatin labeling with streptavidin 525-nm quantum dots (QDs) in a 500- nm semithin epoxy section acquired in 3D-SIM mode. The 100-nm resolution of this <t>microscope</t> resolved the irregular distribution of somatostatin in individual secretory granules. Labeling can be seen to be variable with areas of high and moderate fluorescence (arrows). Intensely stained 500- to 600-nm ring-shaped or “doughnut-like” structures in the cytoplasm (square box) and some nonspecific staining in nuclei (colored blue) may also be seen. Super-resolution imaging of QD probes is possible due to their high photostability and strong fluorescence signal. Objective was ×100 with oil immersion and excitation was with a 488-nm laser (monochrome image with false color). (B) Transmission electron microscopy image showing 500- to 600-nm sized granules with electron-dense material at their margins (arrow) thought to correspond to ring-shaped fluorescent structures. (C) Higher power view of a 500-nm secretory granule with electron-dense material inside the limiting membrane (arrows). Scale bars: A = 8 µm, B = 6 µm, C = 500 nm.
Ni Eclipse Inverted 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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superresolution far field fluorescence microscopy  (Photonics Inc)
86
Photonics Inc superresolution far field fluorescence microscopy
Figure 4. (A) Super-resolution light microscopy image of somatostatin labeling with streptavidin 525-nm quantum dots (QDs) in a 500- nm semithin epoxy section acquired in 3D-SIM mode. The 100-nm resolution of this <t>microscope</t> resolved the irregular distribution of somatostatin in individual secretory granules. Labeling can be seen to be variable with areas of high and moderate fluorescence (arrows). Intensely stained 500- to 600-nm ring-shaped or “doughnut-like” structures in the cytoplasm (square box) and some nonspecific staining in nuclei (colored blue) may also be seen. Super-resolution imaging of QD probes is possible due to their high photostability and strong fluorescence signal. Objective was ×100 with oil immersion and excitation was with a 488-nm laser (monochrome image with false color). (B) Transmission electron microscopy image showing 500- to 600-nm sized granules with electron-dense material at their margins (arrow) thought to correspond to ring-shaped fluorescent structures. (C) Higher power view of a 500-nm secretory granule with electron-dense material inside the limiting membrane (arrows). Scale bars: A = 8 µm, B = 6 µm, C = 500 nm.
Superresolution Far Field Fluorescence Microscopy, supplied by Photonics Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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n storm microscope  (Nikon)
97
Nikon n storm microscope
Figure 4. (A) Super-resolution light microscopy image of somatostatin labeling with streptavidin 525-nm quantum dots (QDs) in a 500- nm semithin epoxy section acquired in 3D-SIM mode. The 100-nm resolution of this <t>microscope</t> resolved the irregular distribution of somatostatin in individual secretory granules. Labeling can be seen to be variable with areas of high and moderate fluorescence (arrows). Intensely stained 500- to 600-nm ring-shaped or “doughnut-like” structures in the cytoplasm (square box) and some nonspecific staining in nuclei (colored blue) may also be seen. Super-resolution imaging of QD probes is possible due to their high photostability and strong fluorescence signal. Objective was ×100 with oil immersion and excitation was with a 488-nm laser (monochrome image with false color). (B) Transmission electron microscopy image showing 500- to 600-nm sized granules with electron-dense material at their margins (arrow) thought to correspond to ring-shaped fluorescent structures. (C) Higher power view of a 500-nm secretory granule with electron-dense material inside the limiting membrane (arrows). Scale bars: A = 8 µm, B = 6 µm, C = 500 nm.
N Storm Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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stedycon system  (abberior instruments)
90
abberior instruments stedycon system
Figure 4. (A) Super-resolution light microscopy image of somatostatin labeling with streptavidin 525-nm quantum dots (QDs) in a 500- nm semithin epoxy section acquired in 3D-SIM mode. The 100-nm resolution of this <t>microscope</t> resolved the irregular distribution of somatostatin in individual secretory granules. Labeling can be seen to be variable with areas of high and moderate fluorescence (arrows). Intensely stained 500- to 600-nm ring-shaped or “doughnut-like” structures in the cytoplasm (square box) and some nonspecific staining in nuclei (colored blue) may also be seen. Super-resolution imaging of QD probes is possible due to their high photostability and strong fluorescence signal. Objective was ×100 with oil immersion and excitation was with a 488-nm laser (monochrome image with false color). (B) Transmission electron microscopy image showing 500- to 600-nm sized granules with electron-dense material at their margins (arrow) thought to correspond to ring-shaped fluorescent structures. (C) Higher power view of a 500-nm secretory granule with electron-dense material inside the limiting membrane (arrows). Scale bars: A = 8 µm, B = 6 µm, C = 500 nm.
Stedycon System, supplied by abberior instruments, 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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fluorescence microscope  (abberior instruments)
90
abberior instruments fluorescence microscope
Figure 4. (A) Super-resolution light microscopy image of somatostatin labeling with streptavidin 525-nm quantum dots (QDs) in a 500- nm semithin epoxy section acquired in 3D-SIM mode. The 100-nm resolution of this <t>microscope</t> resolved the irregular distribution of somatostatin in individual secretory granules. Labeling can be seen to be variable with areas of high and moderate fluorescence (arrows). Intensely stained 500- to 600-nm ring-shaped or “doughnut-like” structures in the cytoplasm (square box) and some nonspecific staining in nuclei (colored blue) may also be seen. Super-resolution imaging of QD probes is possible due to their high photostability and strong fluorescence signal. Objective was ×100 with oil immersion and excitation was with a 488-nm laser (monochrome image with false color). (B) Transmission electron microscopy image showing 500- to 600-nm sized granules with electron-dense material at their margins (arrow) thought to correspond to ring-shaped fluorescent structures. (C) Higher power view of a 500-nm secretory granule with electron-dense material inside the limiting membrane (arrows). Scale bars: A = 8 µm, B = 6 µm, C = 500 nm.
Fluorescence Microscope, supplied by abberior instruments, 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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laser confocal superresolution fluorescence microscope  (Nikon)
99
Nikon laser confocal superresolution fluorescence microscope
Figure 4. (A) Super-resolution light microscopy image of somatostatin labeling with streptavidin 525-nm quantum dots (QDs) in a 500- nm semithin epoxy section acquired in 3D-SIM mode. The 100-nm resolution of this <t>microscope</t> resolved the irregular distribution of somatostatin in individual secretory granules. Labeling can be seen to be variable with areas of high and moderate fluorescence (arrows). Intensely stained 500- to 600-nm ring-shaped or “doughnut-like” structures in the cytoplasm (square box) and some nonspecific staining in nuclei (colored blue) may also be seen. Super-resolution imaging of QD probes is possible due to their high photostability and strong fluorescence signal. Objective was ×100 with oil immersion and excitation was with a 488-nm laser (monochrome image with false color). (B) Transmission electron microscopy image showing 500- to 600-nm sized granules with electron-dense material at their margins (arrow) thought to correspond to ring-shaped fluorescent structures. (C) Higher power view of a 500-nm secretory granule with electron-dense material inside the limiting membrane (arrows). Scale bars: A = 8 µm, B = 6 µm, C = 500 nm.
Laser Confocal Superresolution 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
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laser confocal superresolution fluorescence microscope - by Bioz Stars, 2026-09
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expert line sted microscope  (abberior instruments)
90
abberior instruments expert line sted microscope
Figure 4. (A) Super-resolution light microscopy image of somatostatin labeling with streptavidin 525-nm quantum dots (QDs) in a 500- nm semithin epoxy section acquired in 3D-SIM mode. The 100-nm resolution of this <t>microscope</t> resolved the irregular distribution of somatostatin in individual secretory granules. Labeling can be seen to be variable with areas of high and moderate fluorescence (arrows). Intensely stained 500- to 600-nm ring-shaped or “doughnut-like” structures in the cytoplasm (square box) and some nonspecific staining in nuclei (colored blue) may also be seen. Super-resolution imaging of QD probes is possible due to their high photostability and strong fluorescence signal. Objective was ×100 with oil immersion and excitation was with a 488-nm laser (monochrome image with false color). (B) Transmission electron microscopy image showing 500- to 600-nm sized granules with electron-dense material at their margins (arrow) thought to correspond to ring-shaped fluorescent structures. (C) Higher power view of a 500-nm secretory granule with electron-dense material inside the limiting membrane (arrows). Scale bars: A = 8 µm, B = 6 µm, C = 500 nm.
Expert Line Sted Microscope, supplied by abberior instruments, 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/confocal+fluorescent+microscope+n-storm+superresolution/sted+microscope/10__7554_slash_elife__80622-652-7-6
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superresolution deltavision omx imaging system  (Cytiva Europe)
96
Cytiva Europe superresolution deltavision omx imaging system
Figure 4. (A) Super-resolution light microscopy image of somatostatin labeling with streptavidin 525-nm quantum dots (QDs) in a 500- nm semithin epoxy section acquired in 3D-SIM mode. The 100-nm resolution of this <t>microscope</t> resolved the irregular distribution of somatostatin in individual secretory granules. Labeling can be seen to be variable with areas of high and moderate fluorescence (arrows). Intensely stained 500- to 600-nm ring-shaped or “doughnut-like” structures in the cytoplasm (square box) and some nonspecific staining in nuclei (colored blue) may also be seen. Super-resolution imaging of QD probes is possible due to their high photostability and strong fluorescence signal. Objective was ×100 with oil immersion and excitation was with a 488-nm laser (monochrome image with false color). (B) Transmission electron microscopy image showing 500- to 600-nm sized granules with electron-dense material at their margins (arrow) thought to correspond to ring-shaped fluorescent structures. (C) Higher power view of a 500-nm secretory granule with electron-dense material inside the limiting membrane (arrows). Scale bars: A = 8 µm, B = 6 µm, C = 500 nm.
Superresolution Deltavision Omx Imaging System, supplied by Cytiva Europe, 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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superresolution fluorescence microscopes  (abberior instruments)
90
abberior instruments superresolution fluorescence microscopes
Figure 4. (A) Super-resolution light microscopy image of somatostatin labeling with streptavidin 525-nm quantum dots (QDs) in a 500- nm semithin epoxy section acquired in 3D-SIM mode. The 100-nm resolution of this <t>microscope</t> resolved the irregular distribution of somatostatin in individual secretory granules. Labeling can be seen to be variable with areas of high and moderate fluorescence (arrows). Intensely stained 500- to 600-nm ring-shaped or “doughnut-like” structures in the cytoplasm (square box) and some nonspecific staining in nuclei (colored blue) may also be seen. Super-resolution imaging of QD probes is possible due to their high photostability and strong fluorescence signal. Objective was ×100 with oil immersion and excitation was with a 488-nm laser (monochrome image with false color). (B) Transmission electron microscopy image showing 500- to 600-nm sized granules with electron-dense material at their margins (arrow) thought to correspond to ring-shaped fluorescent structures. (C) Higher power view of a 500-nm secretory granule with electron-dense material inside the limiting membrane (arrows). Scale bars: A = 8 µm, B = 6 µm, C = 500 nm.
Superresolution Fluorescence Microscopes, supplied by abberior instruments, 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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superresolution fluorescence microscopes - by Bioz Stars, 2026-09
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abberior stedycon system  (abberior instruments)
90
abberior instruments abberior stedycon system
Figure 4. (A) Super-resolution light microscopy image of somatostatin labeling with streptavidin 525-nm quantum dots (QDs) in a 500- nm semithin epoxy section acquired in 3D-SIM mode. The 100-nm resolution of this <t>microscope</t> resolved the irregular distribution of somatostatin in individual secretory granules. Labeling can be seen to be variable with areas of high and moderate fluorescence (arrows). Intensely stained 500- to 600-nm ring-shaped or “doughnut-like” structures in the cytoplasm (square box) and some nonspecific staining in nuclei (colored blue) may also be seen. Super-resolution imaging of QD probes is possible due to their high photostability and strong fluorescence signal. Objective was ×100 with oil immersion and excitation was with a 488-nm laser (monochrome image with false color). (B) Transmission electron microscopy image showing 500- to 600-nm sized granules with electron-dense material at their margins (arrow) thought to correspond to ring-shaped fluorescent structures. (C) Higher power view of a 500-nm secretory granule with electron-dense material inside the limiting membrane (arrows). Scale bars: A = 8 µm, B = 6 µm, C = 500 nm.
Abberior Stedycon System, supplied by abberior instruments, 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/confocal+fluorescent+microscope+n-storm+superresolution/abberior+stedycon/pmc06985824-111-8-7
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superresolution re-scanning confocal microscopy system rcm-nir  (confocal nl)
90
confocal nl superresolution re-scanning confocal microscopy system rcm-nir
Figure 4. (A) Super-resolution light microscopy image of somatostatin labeling with streptavidin 525-nm quantum dots (QDs) in a 500- nm semithin epoxy section acquired in 3D-SIM mode. The 100-nm resolution of this <t>microscope</t> resolved the irregular distribution of somatostatin in individual secretory granules. Labeling can be seen to be variable with areas of high and moderate fluorescence (arrows). Intensely stained 500- to 600-nm ring-shaped or “doughnut-like” structures in the cytoplasm (square box) and some nonspecific staining in nuclei (colored blue) may also be seen. Super-resolution imaging of QD probes is possible due to their high photostability and strong fluorescence signal. Objective was ×100 with oil immersion and excitation was with a 488-nm laser (monochrome image with false color). (B) Transmission electron microscopy image showing 500- to 600-nm sized granules with electron-dense material at their margins (arrow) thought to correspond to ring-shaped fluorescent structures. (C) Higher power view of a 500-nm secretory granule with electron-dense material inside the limiting membrane (arrows). Scale bars: A = 8 µm, B = 6 µm, C = 500 nm.
Superresolution Re Scanning Confocal Microscopy System Rcm Nir, supplied by confocal nl, 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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Image Search Results


Figure 4. (A) Super-resolution light microscopy image of somatostatin labeling with streptavidin 525-nm quantum dots (QDs) in a 500- nm semithin epoxy section acquired in 3D-SIM mode. The 100-nm resolution of this microscope resolved the irregular distribution of somatostatin in individual secretory granules. Labeling can be seen to be variable with areas of high and moderate fluorescence (arrows). Intensely stained 500- to 600-nm ring-shaped or “doughnut-like” structures in the cytoplasm (square box) and some nonspecific staining in nuclei (colored blue) may also be seen. Super-resolution imaging of QD probes is possible due to their high photostability and strong fluorescence signal. Objective was ×100 with oil immersion and excitation was with a 488-nm laser (monochrome image with false color). (B) Transmission electron microscopy image showing 500- to 600-nm sized granules with electron-dense material at their margins (arrow) thought to correspond to ring-shaped fluorescent structures. (C) Higher power view of a 500-nm secretory granule with electron-dense material inside the limiting membrane (arrows). Scale bars: A = 8 µm, B = 6 µm, C = 500 nm.

Journal: The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society

Article Title: Quantum dot immunocytochemical localization of somatostatin in somatostatinoma by Widefield Epifluorescence, super-resolution light, and immunoelectron microscopy.

doi: 10.1369/0022155412459856

Figure Lengend Snippet: Figure 4. (A) Super-resolution light microscopy image of somatostatin labeling with streptavidin 525-nm quantum dots (QDs) in a 500- nm semithin epoxy section acquired in 3D-SIM mode. The 100-nm resolution of this microscope resolved the irregular distribution of somatostatin in individual secretory granules. Labeling can be seen to be variable with areas of high and moderate fluorescence (arrows). Intensely stained 500- to 600-nm ring-shaped or “doughnut-like” structures in the cytoplasm (square box) and some nonspecific staining in nuclei (colored blue) may also be seen. Super-resolution imaging of QD probes is possible due to their high photostability and strong fluorescence signal. Objective was ×100 with oil immersion and excitation was with a 488-nm laser (monochrome image with false color). (B) Transmission electron microscopy image showing 500- to 600-nm sized granules with electron-dense material at their margins (arrow) thought to correspond to ring-shaped fluorescent structures. (C) Higher power view of a 500-nm secretory granule with electron-dense material inside the limiting membrane (arrows). Scale bars: A = 8 µm, B = 6 µm, C = 500 nm.

Article Snippet: Superresolution fluorescence microscopy in the present study was performed using a Nikon Ni Eclipse inverted microscope fitted with an N-SIM (Structured Illumination Microscopy) illuminator (Nikon Corporation; Tokyo, Japan).

Techniques: Light Microscopy, Labeling, Microscopy, Fluorescence, Staining, Imaging, Transmission Assay, Electron Microscopy, Membrane