Spinning Disk Confocal Microscopes Search Results


99
Carl Zeiss inverted spinning disc confocal microscope
Inverted Spinning Disc Confocal Microscope, supplied by Carl Zeiss, 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/Spinning+Disk+Confocal+Microscopes/bio_rxiv__2023__10__04__560846-313-8-14?v=Carl+Zeiss
Average 99 stars, based on 1 article reviews
inverted spinning disc confocal microscope - by Bioz Stars, 2026-07
99/100 stars
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99
Nikon ti2 w1 spinning disk confocal microscope
Ti2 W1 Spinning Disk Confocal 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/Spinning+Disk+Confocal+Microscopes/bio_rxiv__2025__02__21__639471-439-6-5?v=Nikon
Average 99 stars, based on 1 article reviews
ti2 w1 spinning disk confocal microscope - by Bioz Stars, 2026-07
99/100 stars
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95
Nikon confocal spinning disk microscope roper nikon
A , Live cells were imaged on a <t>spinning</t> <t>disk</t> <t>microscope</t> during migration through a 2 μm constriction to obtain <t>confocal</t> images at different heights. The images at each timepoint were projected to obtain one image with minimal signal from the SiR-Actin absorbed onto the surfaces of the migration devices. B , Migration times of cells treated with actin or myosin-inhibiting drugs, or control (1:1000 DMSO). (All experiments performed over 3 different days; CTRL, 2 μm N=75, 15 μm N=46; CK666, 2 μm N=40, 15 μm N=50; SMIFH2, 2 μm N=54, 15 μm N=57; PNBlebb, 2 μm N=21, 15 μm N=47; Y-27632 experiments only quantified on day when a data point was obtained for the 2 μm constriction, 2 μm N=1, 15 μm N=25.)
Confocal Spinning Disk Microscope Roper Nikon, supplied by Nikon, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/Spinning+Disk+Confocal+Microscopes/bio_rxiv__713982-276-13-17?v=Nikon
Average 95 stars, based on 1 article reviews
confocal spinning disk microscope roper nikon - by Bioz Stars, 2026-07
95/100 stars
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90
Johns Hopkins HealthCare 3i spinning disk confocal microscope
A , Live cells were imaged on a <t>spinning</t> <t>disk</t> <t>microscope</t> during migration through a 2 μm constriction to obtain <t>confocal</t> images at different heights. The images at each timepoint were projected to obtain one image with minimal signal from the SiR-Actin absorbed onto the surfaces of the migration devices. B , Migration times of cells treated with actin or myosin-inhibiting drugs, or control (1:1000 DMSO). (All experiments performed over 3 different days; CTRL, 2 μm N=75, 15 μm N=46; CK666, 2 μm N=40, 15 μm N=50; SMIFH2, 2 μm N=54, 15 μm N=57; PNBlebb, 2 μm N=21, 15 μm N=47; Y-27632 experiments only quantified on day when a data point was obtained for the 2 μm constriction, 2 μm N=1, 15 μm N=25.)
3i Spinning Disk Confocal Microscope, supplied by Johns Hopkins HealthCare, 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/Spinning+Disk+Confocal+Microscopes/10__1128_slash_iai__01500___13-115-20-30?v=Johns+Hopkins+HealthCare
Average 90 stars, based on 1 article reviews
3i spinning disk confocal microscope - by Bioz Stars, 2026-07
90/100 stars
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90
BFI Optilas GmbH yokogawa csu-22 spinning disc confocal system
A , Live cells were imaged on a <t>spinning</t> <t>disk</t> <t>microscope</t> during migration through a 2 μm constriction to obtain <t>confocal</t> images at different heights. The images at each timepoint were projected to obtain one image with minimal signal from the SiR-Actin absorbed onto the surfaces of the migration devices. B , Migration times of cells treated with actin or myosin-inhibiting drugs, or control (1:1000 DMSO). (All experiments performed over 3 different days; CTRL, 2 μm N=75, 15 μm N=46; CK666, 2 μm N=40, 15 μm N=50; SMIFH2, 2 μm N=54, 15 μm N=57; PNBlebb, 2 μm N=21, 15 μm N=47; Y-27632 experiments only quantified on day when a data point was obtained for the 2 μm constriction, 2 μm N=1, 15 μm N=25.)
Yokogawa Csu 22 Spinning Disc Confocal System, supplied by BFI Optilas GmbH, 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/Spinning+Disk+Confocal+Microscopes/pmc02732900-148-5-11?v=BFI+Optilas+GmbH
Average 90 stars, based on 1 article reviews
yokogawa csu-22 spinning disc confocal system - by Bioz Stars, 2026-07
90/100 stars
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90
Becton Dickinson spinning disk confocal
A , Live cells were imaged on a <t>spinning</t> <t>disk</t> <t>microscope</t> during migration through a 2 μm constriction to obtain <t>confocal</t> images at different heights. The images at each timepoint were projected to obtain one image with minimal signal from the SiR-Actin absorbed onto the surfaces of the migration devices. B , Migration times of cells treated with actin or myosin-inhibiting drugs, or control (1:1000 DMSO). (All experiments performed over 3 different days; CTRL, 2 μm N=75, 15 μm N=46; CK666, 2 μm N=40, 15 μm N=50; SMIFH2, 2 μm N=54, 15 μm N=57; PNBlebb, 2 μm N=21, 15 μm N=47; Y-27632 experiments only quantified on day when a data point was obtained for the 2 μm constriction, 2 μm N=1, 15 μm N=25.)
Spinning Disk Confocal, supplied by Becton Dickinson, 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/Spinning+Disk+Confocal+Microscopes/pmc04792648-98-8-11?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
spinning disk confocal - by Bioz Stars, 2026-07
90/100 stars
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90
3i - Intelligent Imaging custom-built spinning-disc confocal system
A , Live cells were imaged on a <t>spinning</t> <t>disk</t> <t>microscope</t> during migration through a 2 μm constriction to obtain <t>confocal</t> images at different heights. The images at each timepoint were projected to obtain one image with minimal signal from the SiR-Actin absorbed onto the surfaces of the migration devices. B , Migration times of cells treated with actin or myosin-inhibiting drugs, or control (1:1000 DMSO). (All experiments performed over 3 different days; CTRL, 2 μm N=75, 15 μm N=46; CK666, 2 μm N=40, 15 μm N=50; SMIFH2, 2 μm N=54, 15 μm N=57; PNBlebb, 2 μm N=21, 15 μm N=47; Y-27632 experiments only quantified on day when a data point was obtained for the 2 μm constriction, 2 μm N=1, 15 μm N=25.)
Custom Built Spinning Disc Confocal System, supplied by 3i - Intelligent Imaging, 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/Spinning+Disk+Confocal+Microscopes/pmc04395480-255-21-24?v=3i+-+Intelligent+Imaging
Average 90 stars, based on 1 article reviews
custom-built spinning-disc confocal system - by Bioz Stars, 2026-07
90/100 stars
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90
Crisel Instruments fluo-spin up crest confocal microscope
A , Live cells were imaged on a <t>spinning</t> <t>disk</t> <t>microscope</t> during migration through a 2 μm constriction to obtain <t>confocal</t> images at different heights. The images at each timepoint were projected to obtain one image with minimal signal from the SiR-Actin absorbed onto the surfaces of the migration devices. B , Migration times of cells treated with actin or myosin-inhibiting drugs, or control (1:1000 DMSO). (All experiments performed over 3 different days; CTRL, 2 μm N=75, 15 μm N=46; CK666, 2 μm N=40, 15 μm N=50; SMIFH2, 2 μm N=54, 15 μm N=57; PNBlebb, 2 μm N=21, 15 μm N=47; Y-27632 experiments only quantified on day when a data point was obtained for the 2 μm constriction, 2 μm N=1, 15 μm N=25.)
Fluo Spin Up Crest Confocal Microscope, supplied by Crisel 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/Spinning+Disk+Confocal+Microscopes/pm40411871-333-7-21?v=Crisel+Instruments
Average 90 stars, based on 1 article reviews
fluo-spin up crest confocal microscope - by Bioz Stars, 2026-07
90/100 stars
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90
VISITRON Inc spinning disk confocal system
A , Live cells were imaged on a <t>spinning</t> <t>disk</t> <t>microscope</t> during migration through a 2 μm constriction to obtain <t>confocal</t> images at different heights. The images at each timepoint were projected to obtain one image with minimal signal from the SiR-Actin absorbed onto the surfaces of the migration devices. B , Migration times of cells treated with actin or myosin-inhibiting drugs, or control (1:1000 DMSO). (All experiments performed over 3 different days; CTRL, 2 μm N=75, 15 μm N=46; CK666, 2 μm N=40, 15 μm N=50; SMIFH2, 2 μm N=54, 15 μm N=57; PNBlebb, 2 μm N=21, 15 μm N=47; Y-27632 experiments only quantified on day when a data point was obtained for the 2 μm constriction, 2 μm N=1, 15 μm N=25.)
Spinning Disk Confocal System, supplied by VISITRON 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/Spinning+Disk+Confocal+Microscopes/pmc05983578-288-8-12?v=VISITRON+Inc
Average 90 stars, based on 1 article reviews
spinning disk confocal system - by Bioz Stars, 2026-07
90/100 stars
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90
VISITRON Inc visiscope spinning-disc-dc confocal system
A , Live cells were imaged on a <t>spinning</t> <t>disk</t> <t>microscope</t> during migration through a 2 μm constriction to obtain <t>confocal</t> images at different heights. The images at each timepoint were projected to obtain one image with minimal signal from the SiR-Actin absorbed onto the surfaces of the migration devices. B , Migration times of cells treated with actin or myosin-inhibiting drugs, or control (1:1000 DMSO). (All experiments performed over 3 different days; CTRL, 2 μm N=75, 15 μm N=46; CK666, 2 μm N=40, 15 μm N=50; SMIFH2, 2 μm N=54, 15 μm N=57; PNBlebb, 2 μm N=21, 15 μm N=47; Y-27632 experiments only quantified on day when a data point was obtained for the 2 μm constriction, 2 μm N=1, 15 μm N=25.)
Visiscope Spinning Disc Dc Confocal System, supplied by VISITRON 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/Spinning+Disk+Confocal+Microscopes/10__1007_slash_s00396___020___04802___5-63-1-5?v=VISITRON+Inc
Average 90 stars, based on 1 article reviews
visiscope spinning-disc-dc confocal system - by Bioz Stars, 2026-07
90/100 stars
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90
VISITRON Inc spinning disk csu-w1
A , Live cells were imaged on a <t>spinning</t> <t>disk</t> <t>microscope</t> during migration through a 2 μm constriction to obtain <t>confocal</t> images at different heights. The images at each timepoint were projected to obtain one image with minimal signal from the SiR-Actin absorbed onto the surfaces of the migration devices. B , Migration times of cells treated with actin or myosin-inhibiting drugs, or control (1:1000 DMSO). (All experiments performed over 3 different days; CTRL, 2 μm N=75, 15 μm N=46; CK666, 2 μm N=40, 15 μm N=50; SMIFH2, 2 μm N=54, 15 μm N=57; PNBlebb, 2 μm N=21, 15 μm N=47; Y-27632 experiments only quantified on day when a data point was obtained for the 2 μm constriction, 2 μm N=1, 15 μm N=25.)
Spinning Disk Csu W1, supplied by VISITRON 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/Spinning+Disk+Confocal+Microscopes/pm34028531-245-2-1?v=VISITRON+Inc
Average 90 stars, based on 1 article reviews
spinning disk csu-w1 - by Bioz Stars, 2026-07
90/100 stars
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90
Hamamatsu tissuegnostic tissuefaxs sl slide-scanning, spinning disk confocal microscope
A , Live cells were imaged on a <t>spinning</t> <t>disk</t> <t>microscope</t> during migration through a 2 μm constriction to obtain <t>confocal</t> images at different heights. The images at each timepoint were projected to obtain one image with minimal signal from the SiR-Actin absorbed onto the surfaces of the migration devices. B , Migration times of cells treated with actin or myosin-inhibiting drugs, or control (1:1000 DMSO). (All experiments performed over 3 different days; CTRL, 2 μm N=75, 15 μm N=46; CK666, 2 μm N=40, 15 μm N=50; SMIFH2, 2 μm N=54, 15 μm N=57; PNBlebb, 2 μm N=21, 15 μm N=47; Y-27632 experiments only quantified on day when a data point was obtained for the 2 μm constriction, 2 μm N=1, 15 μm N=25.)
Tissuegnostic Tissuefaxs Sl Slide Scanning, Spinning Disk Confocal Microscope, supplied by Hamamatsu, 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/Spinning+Disk+Confocal+Microscopes/bio_rxiv__2022__10__18__512442-352-28-31?v=Hamamatsu
Average 90 stars, based on 1 article reviews
tissuegnostic tissuefaxs sl slide-scanning, spinning disk confocal microscope - by Bioz Stars, 2026-07
90/100 stars
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Image Search Results


A , Live cells were imaged on a spinning disk microscope during migration through a 2 μm constriction to obtain confocal images at different heights. The images at each timepoint were projected to obtain one image with minimal signal from the SiR-Actin absorbed onto the surfaces of the migration devices. B , Migration times of cells treated with actin or myosin-inhibiting drugs, or control (1:1000 DMSO). (All experiments performed over 3 different days; CTRL, 2 μm N=75, 15 μm N=46; CK666, 2 μm N=40, 15 μm N=50; SMIFH2, 2 μm N=54, 15 μm N=57; PNBlebb, 2 μm N=21, 15 μm N=47; Y-27632 experiments only quantified on day when a data point was obtained for the 2 μm constriction, 2 μm N=1, 15 μm N=25.)

Journal: bioRxiv

Article Title: Nesprin-2 accumulates at the front of the nucleus during confined cell migration

doi: 10.1101/713982

Figure Lengend Snippet: A , Live cells were imaged on a spinning disk microscope during migration through a 2 μm constriction to obtain confocal images at different heights. The images at each timepoint were projected to obtain one image with minimal signal from the SiR-Actin absorbed onto the surfaces of the migration devices. B , Migration times of cells treated with actin or myosin-inhibiting drugs, or control (1:1000 DMSO). (All experiments performed over 3 different days; CTRL, 2 μm N=75, 15 μm N=46; CK666, 2 μm N=40, 15 μm N=50; SMIFH2, 2 μm N=54, 15 μm N=57; PNBlebb, 2 μm N=21, 15 μm N=47; Y-27632 experiments only quantified on day when a data point was obtained for the 2 μm constriction, 2 μm N=1, 15 μm N=25.)

Article Snippet: FRAP studies on small regions of the nucleus were performed on an inverted confocal spinning disk microscope (Roper/Nikon) equipped with a FRAP module, a thermostatic chamber, lasers at 405/491/532/561nm, and an EMCCD Evolve camera.

Techniques: Microscopy, Migration