ar1 spinning disk confocal microscope (Nikon)
90
Structured Review
Nikon
ar1 spinning disk confocal microscope
Ar1 Spinning Disk Confocal Microscope, supplied by Nikon, 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/ar1+spinning+disk+confocal+microscope/pm40151891-305-47-46
Average 90 stars, based on 1 article reviews
Ar1 Spinning Disk Confocal Microscope, supplied by Nikon, 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/ar1+spinning+disk+confocal+microscope/pm40151891-305-47-46
Average 90 stars, based on 1 article reviews
ar1 spinning disk confocal microscope - by Bioz Stars,
2026-09
90/100 stars
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Related Articles
Imaging:Article Title: Confinement by Liquid-Liquid Interface Replicates In Vivo Neutrophil Deformations and Elicits Bleb-Based Migration. Article Snippet: Cell motility was visualized on a Nikon epi-fluorescent microscope (Nikon Eclipse TE3000 with a Nikon Plan Fluor 20x/0.50 objective, motorized stage from Ludl Electronic Products and Prime BSI Express camera from Teledyne Photometrics or a Nikon TI Eclipse inverted microscope with Nikon Plan Fluor 20x/0.50 objective and Hamamatsu camera). .. Quantification of cell speed was performed in ImageJ/FIJI using the manual tracking plug-in of time lapse movies taken at time intervals of 30 s. Volumetric imaging of cells interacting with the interface was performed by labeling the media with FITC dye and imaging with the aforementioned Nikon Article Title: Confinement by Liquid‐Liquid Interface Replicates In Vivo Neutrophil Deformations and Elicits Bleb‐Based Migration Article Snippet: Cell motility was visualized on a Nikon epi‐fluorescent microscope (Nikon Eclipse TE3000 with a Nikon Plan Fluor 20x/0.50 objective, motorized stage from Ludl Electronic Products and Prime BSI Express camera from Teledyne Photometrics or a Nikon TI Eclipse inverted microscope with Nikon Plan Fluor 20x/0.50 objective and Hamamatsu camera). .. Quantification of cell speed was performed in ImageJ/FIJI using the manual tracking plug‐in of time lapse movies taken at time intervals of 30 s. Volumetric imaging of cells interacting with the interface was performed by labeling the media with FITC dye and imaging with the aforementioned Nikon Labeling:Article Title: Confinement by Liquid-Liquid Interface Replicates In Vivo Neutrophil Deformations and Elicits Bleb-Based Migration. Article Snippet: Cell motility was visualized on a Nikon epi-fluorescent microscope (Nikon Eclipse TE3000 with a Nikon Plan Fluor 20x/0.50 objective, motorized stage from Ludl Electronic Products and Prime BSI Express camera from Teledyne Photometrics or a Nikon TI Eclipse inverted microscope with Nikon Plan Fluor 20x/0.50 objective and Hamamatsu camera). .. Quantification of cell speed was performed in ImageJ/FIJI using the manual tracking plug-in of time lapse movies taken at time intervals of 30 s. Volumetric imaging of cells interacting with the interface was performed by labeling the media with FITC dye and imaging with the aforementioned Nikon Article Title: Confinement by Liquid‐Liquid Interface Replicates In Vivo Neutrophil Deformations and Elicits Bleb‐Based Migration Article Snippet: Cell motility was visualized on a Nikon epi‐fluorescent microscope (Nikon Eclipse TE3000 with a Nikon Plan Fluor 20x/0.50 objective, motorized stage from Ludl Electronic Products and Prime BSI Express camera from Teledyne Photometrics or a Nikon TI Eclipse inverted microscope with Nikon Plan Fluor 20x/0.50 objective and Hamamatsu camera). .. Quantification of cell speed was performed in ImageJ/FIJI using the manual tracking plug‐in of time lapse movies taken at time intervals of 30 s. Volumetric imaging of cells interacting with the interface was performed by labeling the media with FITC dye and imaging with the aforementioned Nikon Microscopy:Article Title: Confinement by Liquid-Liquid Interface Replicates In Vivo Neutrophil Deformations and Elicits Bleb-Based Migration. Article Snippet: Cell motility was visualized on a Nikon epi-fluorescent microscope (Nikon Eclipse TE3000 with a Nikon Plan Fluor 20x/0.50 objective, motorized stage from Ludl Electronic Products and Prime BSI Express camera from Teledyne Photometrics or a Nikon TI Eclipse inverted microscope with Nikon Plan Fluor 20x/0.50 objective and Hamamatsu camera). .. Quantification of cell speed was performed in ImageJ/FIJI using the manual tracking plug-in of time lapse movies taken at time intervals of 30 s. Volumetric imaging of cells interacting with the interface was performed by labeling the media with FITC dye and imaging with the aforementioned Nikon Article Title: Confinement by Liquid‐Liquid Interface Replicates In Vivo Neutrophil Deformations and Elicits Bleb‐Based Migration Article Snippet: Cell motility was visualized on a Nikon epi‐fluorescent microscope (Nikon Eclipse TE3000 with a Nikon Plan Fluor 20x/0.50 objective, motorized stage from Ludl Electronic Products and Prime BSI Express camera from Teledyne Photometrics or a Nikon TI Eclipse inverted microscope with Nikon Plan Fluor 20x/0.50 objective and Hamamatsu camera). .. Quantification of cell speed was performed in ImageJ/FIJI using the manual tracking plug‐in of time lapse movies taken at time intervals of 30 s. Volumetric imaging of cells interacting with the interface was performed by labeling the media with FITC dye and imaging with the aforementioned Nikon |