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The atomic force microscope uses a different concept to explore microscopic surfaces: touch.
The most common type of confocal microscope uses a single focused laser beam to sequentially point scan a region of a sample.
Unlike standard imaging systems, the light field microscope uses a microlens array to capture both spatial and angular information about the incoming light in a single image, from which a volume can be reconstructed computationally.
The scanning electron microscope uses a beam of electrons to create an image of a surface rather than light.
The Raman microscope uses a back-scattering geometry, where the incident beam is linearly polarized at 500 1 ratio.
The epifluorescent microscope uses a high-pressure mercury lamp that radiates ultraviolet light, which interacts with the fluorescent epoxy resin impregnated within the sample.
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Immunostained cells and microvessels were counted microscopically (Nikon E400 microscope) using a 5 × 5 reticle grid.
Samples were analysed using a Leica TCS SP8 confocal microscope using a 40x original magnification.
Images were acquired on a spinning-disk microscope using a 63× objective.
The images were taken under an Olympus BX60F-3 microscope using a 20x and a 40x original magnification.
The cell layer around the marked areas was then brushed off under the DIC microscope using a fine needle.
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