Qimaging micropublisher 3

Manufactured by Zeiss

The QImaging MicroPublisher 3.3 is a high-resolution digital camera designed for microscopy applications. It features a 3.3-megapixel CCD sensor and can capture images with a resolution of 2048 x 1536 pixels. The camera is compatible with a wide range of microscopes and can be controlled using the included software.

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Lab products found in correlation

Axio imager a1, by Zeiss (2 mentions) 880 lsm nlo airyscan, by Zeiss (2 mentions) Qcapture pro software, by Zeiss (2 mentions) Zen imaging software, by Zeiss (2 mentions)

2 protocols using qimaging micropublisher 3

Super-Resolution Imaging of Gingiva

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Gingiva tissue sections were imaged using super resolution confocal scanning microscopy (Zeiss 880 LSM NLO Airyscan; 1024 × 1024 pixels; magnification: 63x unless specified otherwise) and/or fluorescence microscopy (Zeiss Axio Imager A1 with QImaging MicroPublisher 3.3). The fluorescence was measured at an excitation of 488 nm and emission of 526 for green, an excitation of 561 nm and emission of 650 for red, and excitation of 405 nm and emission of 453 for blue (DAPI). For all samples, 20-35 slices of z-stacks were obtained with each slice at 0.4-0.6µm. A mid-slice within each tissue was chosen for analysis and image presentation. To process data sets, Zeiss Zen imaging software and QCapture Pro software were used for confocal/epifluorescence microscopy, respectively. Representative images were selected to visually display any differences in the antibody staining.

Lee J.S., Spooner R., Chowdhury N., Pandey V., Wellslager B., Atanasova K.R., Evans Z, & Yilmaz Ö. (2020). In Situ Intraepithelial Localizations of Opportunistic Pathogens, Porphyromonas gingivalis and Filifactor alocis, in Human Gingiva. Current Research in Microbial Sciences, 1, 7-17.

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Super-Resolution Imaging of Gingival Tissue

Check if the same lab product or an alternative is used in the 5 most similar protocols

Gingiva tissue sections were imaged using super resolution confocal scanning microscopy (Zeiss 880 LSM NLO Airyscan; 1024 × 1024 pixels; magnification: 63x unless specified otherwise) and/or fluorescence microscopy (Zeiss Axio Imager A1 with QImaging MicroPublisher 3.3). The fluorescence was measured at an excitation of 488 nm and emission of 526 for green, an excitation of 561 nm and emission of 650 for red, and excitation of 405 nm and emission of 453 for blue (DAPI). For all samples, 20-35 slices of z-stacks were obtained with each slice at 0.4-0.6μm. A mid-slice within each tissue was chosen for analysis and image presentation. To process data sets, Zeiss Zen imaging software and QCapture Pro software were used for confocal/epifluorescence microscopy, respectively. Representative images were selected to visually display any differences in the antibody staining.

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