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A light micrograph or photomicrograph is a micrograph prepared using an optical microscope, a process referred to as photomicroscopy.At a basic level, photomicroscopy may be performed simply by connecting a camera to a microscope, thereby enabling the user to take photographs at reasonably high magnification.
Microscope image processing is a broad term that covers the use of digital image processing techniques to process, analyze and present images obtained from a microscope. Such processing is now commonplace in a number of diverse fields such as medicine , biological research , cancer research , drug testing , metallurgy , etc.
Antonie van Leeuwenhoek (1632–1723). The field of microscopy (optical microscopy) dates back to at least the 17th-century.Earlier microscopes, single lens magnifying glasses with limited magnification, date at least as far back as the wide spread use of lenses in eyeglasses in the 13th century [2] but more advanced compound microscopes first appeared in Europe around 1620 [3] [4] The ...
A simple microscope uses a lens or set of lenses to enlarge an object through angular magnification alone, giving the viewer an erect enlarged virtual image. [1] [2] The use of a single convex lens or groups of lenses are found in simple magnification devices such as the magnifying glass, loupes, and eyepieces for telescopes and microscopes.
A bright-field microscope has many important parts including; the condenser, the objective lens, the ocular lens, the diaphragm, and the aperture. Some other pieces of the microscope that are commonly known are the arm, the head, the illuminator, the base, the stage, the adjusters, and the brightness adjuster.
After its introduction in the 1940s, live-cell imaging rapidly became popular using phase-contrast microscopy. [11] The phase-contrast microscope was popularized through a series of time-lapse movies (see video), recorded using a photographic film camera. [12] Its inventor, Frits Zernike, was awarded the Nobel Prize in 1953. [13]
The earliest reference to the use of conoscopy (i.e., observation in convergent light with a polarization microscope with a Bertrand lens) for evaluation of the optical properties of liquid crystalline phases (i.e., orientation of the optical axes) is in 1911 when it was used by Charles-Victor Mauguin to investigate the alignment of nematic and ...
With this new microscope, cellular details could for the first time be observed without using lethal stains. [1] By setting up some of the first time-lapse experiments with chicken fibroblasts and a phase-contrast microscope, Michael Abercrombie described the basis of our current understanding of cell migration in 1953. [23] [24]