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Ultra–large field-of-view two-photon microscopy
Ultra–large field-of-view two-photon microscopy

... The design of the scan system begins with the selection of the objective. We seek a field-ofview that encompasses 10 mm, a numerical aperture (NA) to achieve 1-µm resolution, and a back aperture that does not exceed 25 mm. The singular choice is a 4-times magnification (f = 45 mm), 0.28 NA air-immer ...
Chester F - RIT Center for Imaging Science
Chester F - RIT Center for Imaging Science

... a) To arrive at the correct solution the student must first note which sources are coherent. Light from each beam falls on each of the two slits, and so the light from each beam emerging from the two slits is coherent. But the two beams are not coherent sources with respect to each other. So we have ...
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... Cytomics is going to be important because it is the cell that is the ultimate functional endpoint. The cell is the minimal functional unit within our physiology and thus the functional unit that can be manipulated. Complexity of cell function is only part of why Cytomics will become a major field of ...
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A History of Imaging
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Coherent Optical Information Systems

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... Figure 2 Schematic overview of the undergraduate optical tweezers setup at LION. A laser beam (λ = 658 nm, 65 mW) is sent into the objective with a dichroic mirror. A steering lens placed at the right position, allows for the manipulation of the trap position, while overfilling the back aperture of ...
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Confocal microscopy



Confocal microscopy is an optical imaging technique for increasing optical resolution and contrast of a micrograph by means of adding a spatial pinhole placed at the confocal plane of the lens to eliminate out-of-focus light. It enables the reconstruction of three-dimensional structures from the obtained images. This technique has gained popularity in the scientific and industrial communities and typical applications are in life sciences, semiconductor inspection and materials science.
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