A high-resolution multimode digital microscope system
| Autor: | E D, Salmon, Sidney L, Shaw, Jennifer, Waters, Clare M, Waterman-Storer, Paul S, Maddox, Elaine, Yeh, Kerry, Bloom |
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| Rok vydání: | 2007 |
| Předmět: |
Photomicrography
Optics and Photonics Saccharomyces cerevisiae Proteins Xenopus Green Fluorescent Proteins Mitosis Saccharomyces cerevisiae Microtubules Models Biological Fluorescence Cell Movement Yeasts Image Processing Computer-Assisted Humans Animals Microscopy Phase-Contrast Cells Cultured Lighting Lenses Microscopy Epithelial Cells Signal Processing Computer-Assisted Image Enhancement Cold Temperature Microscopy Fluorescence Mad2 Proteins Single-Cell Analysis Artifacts Algorithms Software |
| Zdroj: | Methods in cell biology. 81 |
| ISSN: | 0091-679X |
| Popis: | This chapter describes the development of a high-resolution, multimode digital imaging system based on a wide-field epifluorescent and transmitted light microscope, and a cooled charge-coupled device (CCD) camera. The three main parts of this imaging system are Nikon FXA microscope, Hamamatsu C4880 cooled CCD camera, and MetaMorph digital imaging system. This chapter presents various design criteria for the instrument and describes the major features of the microscope components-the cooled CCD camera and the MetaMorph digital imaging system. The Nikon FXA upright microscope can produce high resolution images for both epifluorescent and transmitted light illumination without switching the objective or moving the specimen. The functional aspects of the microscope set-up can be considered in terms of the imaging optics, the epi-illumination optics, the transillumination optics, the focus control, and the vibration isolation table. This instrument is somewhat specialized for microtubule and mitosis studies, and it is also applicable to a variety of problems in cellular imaging, including tracking proteins fused to the green fluorescent protein in live cells. The instrument is also valuable for correlating the assembly dynamics of individual cytoplasmic microtubules (labeled by conjugating X-rhodamine to tubulin) with the dynamics of membranes of the endoplasmic reticulum (labeled with DiOC6) and the dynamics of the cell cortex (by differential interference contrast) in migrating vertebrate epithelial cells. This imaging system also plays an important role in the analysis of mitotic mutants in the powerful yeast genetic system Saccharomyces cerevisiae. |
| Databáze: | OpenAIRE |
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