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Vivaview epifluorescence microscope

Manufactured by Olympus

The Vivaview epifluorescence microscope is a laboratory equipment designed for high-resolution fluorescence imaging. It utilizes an epifluorescence illumination system to excite fluorescent samples and capture detailed images. The core function of this microscope is to provide researchers with a tool for visualizing and analyzing fluorescently labeled specimens.

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2 protocols using vivaview epifluorescence microscope

1

Intravital Imaging of Colon Cancer

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Low temporal frequency imaging was performed using an Olympus Vivaview epifluorescence microscope with a sampling interval of 2 minutes. DIC/phase contrast and GFP fluorescence time lapse images were captured before and after stimulation with complexed immunogenic dsDNA. For high frequency time-lapse imaging, we used a Fluoview FV1000 confocal microscope at a scan speed of 2 and sampling interval of 0.5 seconds. Frame sizes are indicated by scale bars. For intravital imaging, dorsal window chambers were installed in adult male reporter mice (8 to 24 weeks old). After window stabilization, 1 million MC38-H2B-mCherry colon cancer cells were injected into the tissue underlying the window and imaging was performed at serial time points.
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2

Intravital Imaging of Colon Cancer

Check if the same lab product or an alternative is used in the 5 most similar protocols
Low temporal frequency imaging was performed using an Olympus Vivaview epifluorescence microscope with a sampling interval of 2 minutes. DIC/phase contrast and GFP fluorescence time lapse images were captured before and after stimulation with complexed immunogenic dsDNA. For high frequency time-lapse imaging, we used a Fluoview FV1000 confocal microscope at a scan speed of 2 and sampling interval of 0.5 seconds. Frame sizes are indicated by scale bars. For intravital imaging, dorsal window chambers were installed in adult male reporter mice (8 to 24 weeks old). After window stabilization, 1 million MC38-H2B-mCherry colon cancer cells were injected into the tissue underlying the window and imaging was performed at serial time points.
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