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543:(1632–1724) is credited with bringing the microscope to the attention of biologists, even though simple magnifying lenses were already being produced in the 16th century. Van Leeuwenhoek's home-made microscopes were simple microscopes, with a single very small, yet strong lens. They were awkward in use, but enabled van Leeuwenhoek to see detailed images. It took about 150 years of optical development before the compound microscope was able to provide the same quality image as van Leeuwenhoek's simple microscopes, due to difficulties in configuring multiple lenses. In the 1850s,
752:, or ocular lens, is a cylinder containing two or more lenses; its function is to bring the image into focus for the eye. The eyepiece is inserted into the top end of the body tube. Eyepieces are interchangeable and many different eyepieces can be inserted with different degrees of magnification. Typical magnification values for eyepieces include 5×, 10× (the most common), 15× and 20×. In some high performance microscopes, the optical configuration of the objective lens and eyepiece are matched to give the best possible optical performance. This occurs most commonly with
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463:, invented the compound microscope and/or the telescope as early as 1590. Johannes' testimony, which some claim is dubious, pushes the invention date so far back that Zacharias would have been a child at the time, leading to speculation that, for Johannes' claim to be true, the compound microscope would have to have been invented by Johannes' grandfather, Hans Martens. Another claim is that Janssen's competitor,
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215:) that gives the viewer an enlarged inverted virtual image of the object (image 2). The use of a compound objective/eyepiece combination allows for much higher magnification. Common compound microscopes often feature exchangeable objective lenses, allowing the user to quickly adjust the magnification. A compound microscope also enables more advanced illumination setups, such as
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molecule produces a diffraction-limited spot of light in the image, and the centre of each of these spots corresponds to the location of the molecule. As the number of fluorescing molecules is low the spots of light are unlikely to overlap and therefore can be placed accurately. This process is then repeated many times to generate the image.
1495:, Alexa dyes, Atto dyes, Cy2/Cy3 and fluorescein molecules can be used for localization microscopy, provided certain photo-physical conditions are present. Using this so-called SPDMphymod (physically modifiable fluorophores) technology a single laser wavelength of suitable intensity is sufficient for nanoimaging.
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At magnifications higher than 100× moving a slide by hand is not practical. A mechanical stage, typical of medium and higher priced microscopes, allows tiny movements of the slide via control knobs that reposition the sample/slide as desired. If a microscope did not originally have a mechanical stage
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The frame provides a mounting point for various microscope controls. Normally this will include controls for focusing, typically a large knurled wheel to adjust coarse focus, together with a smaller knurled wheel to control fine focus. Other features may be lamp controls and/or controls for adjusting
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is sometimes cited as a compound microscope inventor. After 1610, he found that he could close focus his telescope to view small objects, such as flies, close up and/or could look through the wrong end in reverse to magnify small objects. The only drawback was that his 2 foot long telescope had to be
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of a microscope is taken as the ability to distinguish between two closely spaced Airy disks (or, in other words the ability of the microscope to reveal adjacent structural detail as distinct and separate). It is these impacts of diffraction that limit the ability to resolve fine details. The extent
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or water and a matched cover slip between the objective lens and the sample. The refractive index of the index-matching material is higher than air allowing the objective lens to have a larger numerical aperture (greater than 1) so that the light is transmitted from the specimen to the outer face of
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and the objective lens. For example a 10x eyepiece magnification and a 100x objective lens magnification gives a total magnification of 1,000×. Modified environments such as the use of oil or ultraviolet light can increase the resolution and allow for resolved details at magnifications larger than
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Focusing starts at lower magnification in order to center the specimen by the user on the stage. Moving to a higher magnification requires the stage to be moved higher vertically for re-focus at the higher magnification and may also require slight horizontal specimen position adjustment. Horizontal
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Adjustment knobs move the stage up and down with separate adjustment for coarse and fine focusing. The same controls enable the microscope to adjust to specimens of different thickness. In older designs of microscopes, the focus adjustment wheels move the microscope tube up or down relative to the
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is a simple example of how higher resolution surpassing the diffraction limit is possible, but it has major limitations. STED is a fluorescence microscopy technique which uses a combination of light pulses to induce fluorescence in a small sub-population of fluorescent molecules in a sample. Each
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that collect light from the sample. The objective is usually in a cylinder housing containing a glass single or multi-element compound lens. Typically there will be around three objective lenses screwed into a circular nose piece which may be rotated to select the required objective lens. These
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lenses with different magnification are usually provided mounted on a turret, allowing them to be rotated into place and providing an ability to zoom-in. The maximum magnification power of optical microscopes is typically limited to around 1000x because of the limited resolving power of visible
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Multiple techniques are available for reaching resolutions higher than the transmitted light limit described above. Holographic techniques, as described by
Courjon and Bulabois in 1979, are also capable of breaking this resolution limit, although resolution was restricted in their experimental
2837:
Bradl, Joachim (1996). "Comparative study of three-dimensional localization accuracy in conventional, confocal laser scanning and axial tomographic fluorescence light microscopy". In Bigio, Irving J; Grundfest, Warren S; Schneckenburger, Herbert; Svanberg, Katarina; Viallet, Pierre M (eds.).
1599:). The specimen chambers needed for all such instruments also limits sample size, and sample manipulation is more difficult. Color cannot be seen in images made by these methods, so some information is lost. They are however, essential when investigating molecular or atomic effects, such as
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the objective lens with minimal refraction. Numerical apertures as high as 1.6 can be achieved. The larger numerical aperture allows collection of more light making detailed observation of smaller details possible. An oil immersion lens usually has a magnification of 40 to 100×.
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to generate magnified images of small objects. Optical microscopes are the oldest design of microscope and were possibly invented in their present compound form in the 17th century. Basic optical microscopes can be very simple, although many complex designs aim to improve
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All modern optical microscopes designed for viewing samples by transmitted light share the same basic components of the light path. In addition, the vast majority of microscopes have the same 'structural' components (numbered below according to the image on the right):
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Modern microscopes allow more than just observation of transmitted light image of a sample; there are many techniques which can be used to extract other kinds of data. Most of these require additional equipment in addition to a basic compound microscope.
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Aspden, Reuben S.; Gemmell, Nathan R.; Morris, Peter A.; Tasca, Daniel S.; Mertens, Lena; Tanner, Michael G.; Kirkwood, Robert A.; Ruggeri, Alessandro; Tosi, Alberto; Boyd, Robert W.; Buller, Gerald S.; Hadfield, Robert H.; Padgett, Miles J. (2015).
364:. Microscopes can also be partly or wholly computer-controlled with various levels of automation. Digital microscopy allows greater analysis of a microscope image, for example, measurements of distances and areas and quantitation of a fluorescent or
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STM and AFM are scanning probe techniques using a small probe which is scanned over the sample surface. Resolution in these cases is limited by the size of the probe; micromachining techniques can produce probes with tip radii of 5–10 nm.
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The use of electrons and X-rays in place of light allows much higher resolution – the wavelength of the radiation is shorter so the diffraction limit is lower. To make the short-wavelength probe non-destructive, the atomic beam imaging system
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The whole of the optical assembly is traditionally attached to a rigid arm, which in turn is attached to a robust U-shaped foot to provide the necessary rigidity. The arm angle may be adjustable to allow the viewing angle to be adjusted.
575:. This method of sample illumination gives rise to extremely even lighting and overcomes many limitations of older techniques of sample illumination. Before development of Köhler illumination the image of the light source, for example a
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of a single lens or group of lenses for magnification. A compound microscope uses a system of lenses (one set enlarging the image produced by another) to achieve a much higher magnification of an object. The vast majority of modern
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It is important to note that higher frequency waves have limited interaction with matter, for example soft tissues are relatively transparent to X-rays resulting in distinct sources of contrast and different target applications.
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for light microscopy. "Optically isolated" means that at a given point in time, only a single particle/molecule within a region of a size determined by conventional optical resolution (typically approx. 200–250 nm
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The stage is a platform below the objective lens which supports the specimen being viewed. In the center of the stage is a hole through which light passes to illuminate the specimen. The stage usually has arms to hold
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of the Max Planck
Institute for Biophysical Chemistry was awarded the 10th German Future Prize in 2006 and Nobel Prize for Chemistry in 2014 for his development of the STED microscope and associated methodologies.
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Journal of the Royal
Microscopical Society, Containing Its Transactions and Proceedings and a Summary of Current Researches Relating to Zoology and Botany (Principally Invertebrata and Cryptogamia), Microscopy,
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While basic microscope technology and optics have been available for over 400 years it is much more recently that techniques in sample illumination were developed to generate the high quality images seen today.
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Lemmer, P.; Gunkel, M.; Baddeley, D.; Kaufmann, R.; Urich, A.; Weiland, Y.; Reymann, J.; Müller, P.; Hausmann, M.; Cremer, C. (2008). "SPDM: light microscopy with single-molecule resolution at the nanoscale".
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port to show the images directly on the monitor. They offer modest magnifications (up to about 200×) without the need to use eyepieces and at a very low cost. High-power illumination is usually provided by an
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Kaufmann, R; Müller, P; Hildenbrand, G; Hausmann, M; Cremer, C; et al. (2011). "Analysis of Her2/neu membrane protein clusters in different types of breast cancer cells using localization microscopy".
270:, whose design usually includes a polarizing filter, rotating stage, and gypsum plate to facilitate the study of minerals or other crystalline materials whose optical properties can vary with orientation.
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to photon-sparse microscopy, the sample is illuminated with infrared photons, each spatially correlated with an entangled partner in the visible band for efficient imaging by a photon-counting camera.
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are simple single-lens microscopes. Compound microscopes can be further divided into a variety of other types of microscopes, which differ in their optical configurations, cost, and intended purposes.
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Due to the difficulty in preparing specimens and mounting them on slides, for children it is best to begin with prepared slides that are centered and focus easily regardless of the focus level used.
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corrected, and therefore a huge step forward in microscope development. The
Huygens ocular is still being produced to this day, but suffers from a small field size, and other minor disadvantages.
2075:, p. 28) makes it unlikely he invented it in 1590 and the claim of invention is based on the testimony of Zacharias Janssen's son, Johannes Zachariassen, who may have fabricated the whole story (
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3D super resolution microscopy with standard fluorescent dyes can be achieved by combination of localization microscopy for standard fluorescent dyes SPDMphymod and structured illumination SMI.
2129:
Robert D. Huerta, Giants of Delft: Johannes
Vermeer and the Natural Philosophers : the Parallel Search for Knowledge During the Age of Discovery, Bucknell University Press - 2003, page 126
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Note: stories vary, including
Zacharias Janssen had the help of his father Hans Martens (or sometimes said to have been built entirely by his father). Zacharias' probable birth date of 1585 (
467:(who applied for the first telescope patent in 1608) also invented the compound microscope. Other historians point to the Dutch innovator Cornelis Drebbel with his 1621 compound microscope.
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associated with long workdays at a microscopy station. In certain applications, long-working-distance or long-focus microscopes are beneficial. An item may need to be examined behind a
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3082:"Metallographic and Materialographic Specimen Preparation, Light Microscopy, Image Analysis and Hardness Testing", Kay Geels in collaboration with Struers A/S, ASTM International 2006.
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There are many variants of the compound optical microscope design for specialized purposes. Some of these are physical design differences allowing specialization for certain purposes:
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the sample is illuminated through the objective lens with a narrow set of wavelengths of light. This light interacts with fluorophores in the sample which then emit light of a longer
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extended out to 6 feet to view objects that close. After seeing the compound microscope built by
Drebbel exhibited in Rome in 1624, Galileo built his own improved version. In 1625,
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Lee, Joonhee; Crampton, Kevin T.; Tallarida, Nicholas; Apkarian, V. Ara (April 2019). "Visualizing vibrational normal modes of a single molecule with atomically confined light".
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Student microscope – an often low-power microscope with simplified controls and sometimes low-quality optics designed for school use or as a starter instrument for children.
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Additionally, methods such as electron or X-ray microscopy use a vacuum or partial vacuum, which limits their use for live and biological samples (with the exception of an
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obtainable with conventional lenses is about 200 nm. A new type of lens using multiple scattering of light allowed to improve the resolution to below 100 nm.
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Van Putten, E. G.; Akbulut, D.; Bertolotti, J.; Vos, W. L.; Lagendijk, A.; Mosk, A. P. (2011). "Scattering Lens
Resolves Sub-100 nm Structures with Visible Light".
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The actual inventor of the compound microscope is unknown although many claims have been made over the years. These include a claim 35 years after they appeared by
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While most techniques focus on increases in lateral resolution there are also some techniques which aim to allow analysis of extremely thin samples. For example,
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to allow viewing of tiny particles whose diameter is below or near the wavelength of visible light (around 500 nanometers); mostly obsolete since the advent of
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Objective turret, revolver, or revolving nose piece is the part that holds the set of objective lenses. It allows the user to switch between objective lenses.
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2620:
Courjon, D.; Bulabois, J. (1979). "Real Time
Holographic Microscopy Using a Peculiar Holographic Illuminating System and a Rotary Shearing Interferometer".
1295:(NA) of the objective lens. There is therefore a finite limit beyond which it is impossible to resolve separate points in the objective field, known as the
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All stages move up and down for focus. With a mechanical stage slides move on two horizontal axes for positioning the specimen to examine specimen details.
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551:, invented the first practical binocular microscope while carrying out one of the earliest and most extensive American microscopic investigations of
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In order to overcome the limitations set by the diffraction limit of visible light other microscopes have been designed which use other waves.
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A simple microscope uses a lens or set of lenses to enlarge an object through angular magnification alone, giving the viewer an erect enlarged
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Cremer, Christoph; Hausmann, Michael; Bradl, Joachim and Rinke, Bernd "Method and devices for measuring distances between object structures",
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The sample can be lit in a variety of ways. Transparent objects can be lit from below and solid objects can be lit with light coming through (
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Optical microscopy is used extensively in microelectronics, nanophysics, biotechnology, pharmaceutic research, mineralogy and microbiology.
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of about 40 to 2 mm, respectively. Objective lenses with higher magnifications normally have a higher numerical aperture and a shorter
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Cremer, Christoph; Hausmann, Michael; Bradl, Joachim and
Schneider, Bernhard "Wave field microscope with detection point spread function",
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is a lens designed to focus light from the illumination source onto the sample. The condenser may also include other features, such as a
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methods place the thin sample on a contrast-enhancing surface and thereby allows to directly visualize films as thin as 0.3 nanometers.
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in the resulting image. Some high performance objective lenses may require matched eyepieces to deliver the best optical performance.
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which allows position, distance and angle measurements on "optically isolated" particles (e.g. molecules) well below the theoretical
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339:
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Heintzmann, Rainer (1999). Bigio, Irving J.; Schneckenburger, Herbert; Slavik, Jan; Svanberg, Katarina; Viallet, Pierre M. (eds.).
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Despite significant progress in the last decade, techniques for surpassing the diffraction limit remain limited and specialized.
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1588:) has been proposed and widely discussed in the literature, but it is not yet competitive with conventional imaging systems.
2002:
J. William Rosenthal, Spectacles and Other Vision Aids: A History and Guide to Collecting, Norman Publishing, 1996, page 391
1974:
William Rosenthal, Spectacles and Other Vision Aids: A History and Guide to Collecting, Norman Publishing, 1996, pp. 391–392
1938:
Atti Della Fondazione Giorgio Ronchi E Contributi Dell'Istituto Nazionale Di Ottica, Volume 30, La Fondazione-1975, page 554
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Digital microscopy with very low light levels to avoid damage to vulnerable biological samples is available using sensitive
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of the object inside the microscope (image 1). That image is then magnified by a second lens or group of lenses (called the
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There are two basic types of optical microscopes: simple microscopes and compound microscopes. A simple microscope uses the
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A. Mark Smith, From Sight to Light: The Passage from Ancient to Modern Optics, University of Chicago Press - 2014, page 387
1237:, or industrial subjects may be a hazard to the objective. Such optics resemble telescopes with close-focus capabilities.
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1922:
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SPDM (spectral precision distance microscopy), the basic localization microscopy technology is a light optical process of
294:, a widely used variant of epifluorescent illumination that uses a scanning laser to illuminate a sample for fluorescence.
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2247:
Cassedy JH (1973). "John L. Riddell's Vibrio biceps: Two documents on American microscopy and cholera etiology 1849–59".
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3D dual color super resolution microscopy with Her2 and Her3 in breast cells, standard dyes: Alexa 488, Alexa 568 LIMON
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within such a region all carry different spectral markers (e.g. different colors or other usable differences in the
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510:(skopein) meaning "to look at", a name meant to be analogous with "telescope", another word coined by the Linceans.
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Very small, portable microscopes have found some usage in places where a laboratory microscope would be a burden.
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300:, used to image fluorescence deeper in scattering media and reduce photobleaching, especially in living samples.
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84:, slightly different images are used to create a 3-D effect. A camera is typically used to capture the image (
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171:. The use of a single convex lens or groups of lenses are found in simple magnification devices such as the
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and/or filters, to manage the quality and intensity of the illumination. For illumination techniques like
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234:, a low-powered microscope which provides a stereoscopic view of the sample, commonly used for dissection.
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799:. The former typically ranges from 5× to 100× while the latter ranges from 0.14 to 0.7, corresponding to
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At very high magnifications with transmitted light, point objects are seen as fuzzy discs surrounded by
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881:(rectangular glass plates with typical dimensions of 25×75 mm, on which the specimen is mounted).
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on the microscope. In high-power microscopes, both eyepieces typically show the same image, but with a
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3113:, an illustrated collection with more than 3000 photos of scientific microscopes by European makers
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1988:
Raymond J. Seeger, Men of Physics: Galileo Galilei, His Life and His Works, Elsevier - 2016, page 24
326:, without traditional wavelength-based resolution limits. This microscope primarily realized on the
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can be used to increase image contrast by highlighting small details of differing refractive index.
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Laterally modulated excitation microscopy: improvement of resolution by using a diffraction grating
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for specific structures within a cell. In contrast to normal transilluminated light microscopy, in
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graduated to allow measuring distances in the focal plane. The other (and older) type has simple
787:, which means that when one changes from one lens to another on a microscope, the sample stays in
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light. While larger magnifications are possible no additional details of the object are resolved.
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1394:. In 2005, a microscope capable of detecting a single molecule was described as a teaching tool.
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has two separate light paths allowing direct comparison of two samples via one image in each eye.
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Measuring microscopes are used for precision measurement. There are two basic types. One has a
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image from a sample. Major techniques for generating increased contrast from the sample include
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or water-immersion objectives for greater resolution at high magnification. These are used with
652:, have been used to label specific structures within the cell. More recent developments include
203:
A compound microscope uses a lens close to the object being viewed to collect light (called the
2485:
1299:. Assuming that optical aberrations in the whole optical set-up are negligible, the resolution
907:. Most microscopes, however, have their own adjustable and controllable light source – often a
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cells, can be imaged without having to use staining techniques. Just two years later, in 1955,
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with limited magnification, which date at least as far back as the widespread use of lenses in
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SMI (spatially modulated illumination microscopy) is a light optical process of the so-called
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516:, another Dutchman, developed a simple 2-lens ocular system in the late 17th century that was
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of the illuminating light, or to extract other structural parameters in the nanometer range.
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in a suitable manner to either increase the optical resolution, to maximize the precision of
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may minimize the risk of damage to the most light-sensitive samples. In this application of
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Objective turret, revolver, or revolving nose piece (to hold multiple objective lenses) (2)
246:, for studying samples from below; useful for cell cultures in liquid or for metallography.
138:
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In industrial use, binocular microscopes are common. Aside from applications needing true
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100:
3122:, A collection of 17th through 19th century microscopes, including extensive descriptions
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1900:
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Compound microscopes first appeared in Europe around 1620 including one demonstrated by
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Fiber optic connector inspection microscope, designed for connector end-face inspection
216:
2871:"High-precision measurements in epifluorescent microscopy – simulation and experiment"
2147:
Daniel J. Boorstin, The Discoverers, Knopf Doubleday Publishing Group - 2011, page 327
1771:
Kumar, Naresh; Weckhuysen, Bert M.; Wain, Andrew J.; Pollard, Andrew J. (April 2019).
1515:
Stimulated emission depletion (STED) microscopy image of actin filaments within a cell
1049:
Four examples of transilumination techniques used to generate contrast in a sample of
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microscopy additional optical components must be precisely aligned in the light path.
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2751:. Optical Biopsies and Microscopic Techniques III. Vol. 3568. pp. 185–196.
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2656:"Demonstration of a Low-Cost, Single-Molecule Capable, Multimode Optical Microscope"
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Multiple transmission microscopy for contrast enhancement and aberration reduction.
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and specific contrast-enhanced slides for the visualization of nanometric samples.
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800:
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17:
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Many techniques are available which modify the light path to generate an improved
2842:. Optical Biopsies and Microscopic Techniques. Vol. 2926. pp. 201–206.
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2159:
2157:
Gould, Stephen Jay (2000). "Chapter 2: The Sharp-Eyed Lynx, Outfoxed by Nature".
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At the lower end of a typical compound optical microscope, there are one or more
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digital cameras. It has been demonstrated that a light source providing pairs of
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technique, placing the specimen on a glass slide and mixing with a salt solution
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528:
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1881:
1170:(where a UV-visible spectrophotometer is integrated with an optical microscope)
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Reflected light, or incident, illumination (for analysis of surface structures)
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Many sources of light can be used. At its simplest, daylight is directed via a
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and a micrometer mechanism for moving the subject relative to the microscope.
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to recognise specific proteins within a sample, and fluorescent proteins like
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The oldest published image known to have been made with a microscope: bees by
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Other microscope variants are designed for different illumination techniques:
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85:
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1918:
1882:"Photon-sparse microscopy: visible light imaging using infrared illumination"
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1291:(λ), the refractive materials used to manufacture the objective lens and the
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specimen position adjustments are the reason for having a mechanical stage.
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CLEO:2011 - Laser Applications to Photonic Applications (2011), Paper CThW6
1857:
1806:
2268:
1378:
Using fluorescent samples more techniques are available. Examples include
118:
Alternatives to optical microscopy which do not use visible light include
2161:
The Lying Stones of Marrakech: Penultimate Reflections in Natural History
1612:
1477:
1444:
964:
749:
743:
361:
212:
180:
152:
77:
2687:
1241:
552:
3119:
3098:
2847:
2756:
1998:
1996:
1994:
1182:
Automation (for automatic scanning of a large sample or image capture)
3268:
3149:
3104:
1401:
1350:
Usually a wavelength of 550 nm is assumed, which corresponds to
1038:
963:
of a compound optical microscope is the product of the powers of the
904:
791:. Microscope objectives are characterized by two parameters, namely,
720:
376:
3139:
3088:, Siegfried Weisenburger and Vahid Sandoghdar, arXiv:1412.3255 2014.
155:
microscopes are compound microscopes, while some cheaper commercial
1447:
measurements of fluorescent objects that are small relative to the
1283:
and magnitude of the diffraction patterns are affected by both the
626:
Modern biological microscopy depends heavily on the development of
594:
illumination which allows imaging of transparent samples. By using
3085:
2573:
2535:"If You've Ever Wanted a Smartphone Microscope, Now's Your Chance"
1984:
1982:
1980:
1773:"Nanoscale chemical imaging using tip-enhanced Raman spectroscopy"
1510:
1362:
is 0.95, and with oil, up to 1.5. In practice the lowest value of
1351:
1288:
1258:
1190:
975:
916:
814:
716:
675:
527:
338:
194:
176:
137:
103:
may be used to determine crystal orientation of metallic objects.
2392:
By Katarina Logg. Chalmers Dept. Applied Physics. 20 January 2006
2340:"Contrast Enhancement by Multi-Pass Phase-Conjugation Microscopy"
1439:(PSF) engineering. These are processes which modify the PSF of a
3101:
A site about Antique Microscopes, their Accessories, and History
645:
644:
Since the mid-20th century chemical fluorescent stains, such as
3153:
2919:"Dual color localization microscopy of cellular nanostructures"
2716:"2 Americans and a German Are Awarded Nobel Prize in Chemistry"
912:
649:
393:
388:
288:, designed for analysis of samples that include fluorophores.
452:
in London (around 1621) and one exhibited in Rome in 1624.
130:
and as a result, can achieve much greater magnifications.
579:
filament, was always visible in the image of the sample.
375:, are also commercially available. These are essentially
3333:
Total internal reflection fluorescence microscopy (TIRF)
2307:
Kenneth, Spring; Keller, H. Ernst; Davidson, Michael W.
2195:, Instituto e Museo di Storia della Scienza (in Italian)
823:
microscope objective lenses: 100× (left) and 40× (right)
3057:
Van Helden, Albert; Dupre, Sven; Van Gent, Rob (2011).
459:
spectacle-maker Johannes Zachariassen that his father,
282:, which applies the phase contrast illumination method.
3086:"Light Microscopy: An ongoing contemporary revolution"
2338:
Pégard, Nicolas C.; Fleischer, Jason W. (1 May 2011).
1128:
of different path lengths of light through the sample.
680:
Basic optical transmission microscope elements (1990s)
602:
of light, extremely transparent samples, such as live
1312:
1263:
The diffraction limit set in stone on a monument for
1086:
illumination, sample contrast comes from rotation of
641:. It is this emitted light which makes up the image.
482:
for the compound microscope Galileo submitted to the
356:
A digital microscope is a microscope equipped with a
36:
Scientist using an optical microscope in a laboratory
3371:
Photo-activated localization microscopy (PALM/STORM)
2012:
Albert Van Helden; Sven Dupré; Rob van Gent (2010).
1948:
Albert Van Helden; Sven Dupré; Rob van Gent (2010).
3351:
3296:
3209:
2088:
Brian Shmaefsky, Biotechnology 101 - 2006, page 171
760:
Objective turret (revolver or revolving nose piece)
2228:Riddell JL (1854). "On the binocular microscope".
2158:
2018:. Amsterdam University Press. pp. 32–36, 43.
1715:The Principles and Practice of Electron Microscopy
1657:"Lesson 2 – Page 3, CLASSIFICATION OF MICROSCOPES"
1339:
387:. The camera is attached directly to a computer's
923:is often provided on more expensive instruments.
3099:Antique Microscopes & Scientific Instruments
1685:The IIT Foundation Series - Physics Class 8, 2/e
1195:A 40x magnification image of cells in a medical
3134:Online tutorial of practical optical microscopy
3029:"German Future Prize for crossing Abbe's Limit"
1105:illumination, sample contrast comes from light
396:source or sources adjacent to the camera lens.
2869:Heintzmann, R.; Münch, H.; Cremer, C. (1997).
2681:Ritter, Karl; Rising, Malin (8 October 2014).
1358:as the external medium, the highest practical
322:, is a variant of optical microscope based on
76:and may be directly viewed through one or two
3274:Interference reflection microscopy (IRM/RICM)
3165:
1480:) is being registered. This is possible when
483:
8:
2523:A discussion of Zeiss measuring microscopes.
1199:taken through an optical microscope using a
2840:Optical Biopsies and Microscopic Techniques
2683:"2 Americans, 1 German win chemistry Nobel"
2490:Encyclopedia of Optical Engineering, Vol. 3
2403:"Long-focus microscope with camera adapter"
3172:
3158:
3150:
1954:. Amsterdam University Press. p. 24.
1597:environmental scanning electron microscope
586:in physics was awarded to Dutch physicist
2988:
2572:
1908:
1788:
1718:. Cambridge University Press. p. 6.
1340:{\displaystyle d={\frac {\lambda }{2NA}}}
1319:
1311:
1124:illumination, sample contrast comes from
1067:illumination, sample contrast comes from
276:, similar to the petrographic microscope.
3244:Differential interference contrast (DIC)
1740:"Buying a cheap microscope for home use"
1688:. Pearson Education India. p. 213.
1458:
309:, an adapted light microscope that uses
31:
1647:
1047:
360:allowing observation of a sample via a
3239:Quantitative phase-contrast microscopy
2891:from the original on 16 February 2016.
1707:
1705:
1423:for the development of super-resolved
1384:near field scanning optical microscopy
919:are becoming a more common provision.
2533:Linder, Courtney (22 November 2019).
490:in 1624 (Galileo had called it the "
434:The earliest microscopes were single
7:
3401:
3366:Stimulated emission depletion (STED)
2695:from the original on 11 October 2014
2413:from the original on 3 October 2011.
2319:from the original on 1 November 2008
2111:from the original on 3 February 2017
1491:Many standard fluorescent dyes like
1229:, the use of dual eyepieces reduces
656:, which uses fluorescently labelled
2917:Manuel Gunkel; et al. (2009).
2728:from the original on 9 October 2014
1553:Scanning ion-conductance microscopy
1222:on free cells or tissue fragments.
498:"). Faber coined the name from the
2346:. Optica Publishing Group: CThW6.
2313:Olympus Microscopy Resource Center
2283:"How to Use a Compound Microscope"
1455:Localization microscopy SPDMphymod
1037:illumination. A recent technique (
1035:differential interference contrast
949:differential interference contrast
612:differential interference contrast
330:platforms using all optical tools.
27:Microscope that uses visible light
25:
3338:Lightsheet microscopy (LSFM/SPIM)
3107:A collection of early microscopes
3035:from the original on 7 March 2009
2714:Chang, Kenneth (8 October 2014).
2662:from the original on 6 March 2009
1928:from the original on 4 June 2016.
1752:from the original on 5 March 2016
1218:when dealing with tissues, or in
425:Timeline of microscope technology
371:Low-powered digital microscopes,
3400:
3389:
3388:
3287:
3130:, concepts in optical microscopy
2999:10.1111/j.1365-2818.2010.03436.x
2963:from the original on 3 May 2019.
2488:. In Driggers, Ronald G. (ed.).
1663:from the original on 10 May 2016
1565:Transmission electron microscopy
1114:
1095:
1076:
1057:
783:arrangements are designed to be
712:Stage (to hold the specimen) (6)
701:Focus knobs (to move the stage)
199:Diagram of a compound microscope
124:transmission electron microscopy
2076:
2072:
2038:
1370:Surpassing the resolution limit
1210:Optical microscopy is used for
885:it may be possible to add one.
590:in 1953 for his development of
324:tip-enhanced Raman spectroscopy
255:, for studying samples of high
3343:Lattice light-sheet microscopy
3254:Second harmonic imaging (SHIM)
3061:. Amsterdam University Press.
2907:priority date 23 December 1996
2591:10.1103/PhysRevLett.106.193905
2099:"Who Invented the Microscope?"
1499:3D super resolution microscopy
1146:Fluorescence microscopy, both:
911:, although illumination using
506:(micron) meaning "small", and
142:Diagram of a simple microscope
1:
2425:"Questar Maksutov microscope"
2207:The Lying Stones of Marrakech
1559:Scanning tunneling microscope
1520:Stimulated emission depletion
1392:stimulated emission depletion
855:stand and had a fixed stage.
833:Some microscopes make use of
320:Tip-enhanced Raman microscope
3059:The Origins of the Telescope
2783:, priority date 10 July 1997
2015:The Origins of the Telescope
1951:The Origins of the Telescope
1547:Scanning electron microscope
547:, Professor of Chemistry at
120:scanning electron microscopy
2492:. CRC Press. p. 2409.
2455:"FTA long-focus microscope"
2186:"Il microscopio di Galileo"
1431:Structured illumination SMI
3455:
3136:at University of Cambridge
2642:10.1088/0150-536X/10/3/004
2352:10.1364/CLEO_SI.2011.CThW6
2261:10.1093/jhmas/xxviii.2.101
2204:Gould, Stephen Jay (2000)
2165:. New York, N.Y: Harmony.
1682:Trisha Knowledge Systems.
1154:Epifluorescence microscopy
1010:
985:Office of Field Operations
826:
771:
741:
689:Eyepiece (ocular lens) (1)
618:-based imaging technique.
418:
349:
286:Epifluorescence microscope
72:The object is placed on a
3384:
3285:
3187:
2816:10.1007/s00340-008-3152-x
1842:10.1038/s41586-019-1059-9
1790:10.1038/s41596-019-0132-z
1488:of different particles).
1214:, the field being termed
1090:light through the sample.
610:published the theory for
484:
383:and generally do not use
328:scanning-probe microscope
280:Phase-contrast microscope
223:Other microscope variants
128:scanning probe microscopy
2484:Ollsson, Gustaf (2003).
2050:Shmaefsky, Brian (2006)
1409:Nobel Prize in Chemistry
1274:rings. These are called
1176:Near-Infrared microscopy
835:oil-immersion objectives
44:, also referred to as a
3304:Fluorescence microscopy
3264:Structured illumination
3219:Bright-field microscopy
3105:Antique Microscopes.com
2561:Physical Review Letters
2388:24 January 2011 at the
2309:"Microscope objectives"
1910:10.1364/OPTICA.2.001049
1541:Atomic force microscope
1469:fluorescence microscopy
1425:fluorescence microscopy
1407:On 8 October 2014, the
1071:of light in the sample.
1007:Illumination techniques
839:index-matching material
811:Oil immersion objective
668:making it fluorescent.
635:fluorescence microscopy
622:Fluorescence microscopy
541:Antonie van Leeuwenhoek
268:Petrographic microscope
207:lens), which focuses a
3376:Near-field (NSOM/SNOM)
3314:Multiphoton microscopy
3145:Cell Centered Database
3111:Historical microscopes
2938:10.1002/biot.200900005
1570:Ultraviolet microscope
1516:
1464:
1341:
1267:
1204:
1173:Ultraviolet microscopy
1003:
824:
738:Eyepiece (ocular lens)
681:
664:which a live cell can
537:
347:
200:
143:
105:Phase-contrast imaging
99:) the objective lens.
37:
3229:Dark-field microscopy
3127:Molecular Expressions
2977:Journal of Microscopy
2926:Biotechnology Journal
2904:U.S. patent 6,424,421
2780:U.S. patent 7,342,717
2459:firsttenangstroms.com
2383:O1 Optical Microscopy
2107:. 14 September 2013.
2054:. Greenwood. p. 171.
1745:. Oxford University.
1514:
1462:
1437:point spread function
1342:
1262:
1194:
1084:Cross-polarized light
1043:cross-polarized light
1023:cross-polarized light
997:international airport
979:
818:
704:Coarse adjustment (4)
679:
531:
445:in the 13th century.
342:
298:Two-photon microscope
274:Polarizing microscope
238:Comparison microscope
198:
141:
35:
3297:Fluorescence methods
3120:The Golub Collection
2521:. 1906. p. 716.
2191:9 April 2008 at the
1712:Ian M. Watt (1997).
1310:
1303:, can be stated as:
959:The actual power or
733:Mechanical stage (9)
614:microscopy, another
545:John Leonard Riddell
486:Accademia dei Lincei
379:with a high-powered
315:electron microscopes
253:Traveling microscope
3328:Image deconvolution
3309:Confocal microscopy
3249:Dispersion staining
3224:Köhler illumination
2808:2008ApPhB..93....1L
2634:1979JOpt...10..125C
2583:2011PhRvL.106s3905V
2465:on 26 February 2012
1901:2015Optic...2.1049A
1834:2019Natur.568...78L
1631:Köhler illumination
1473:limit of resolution
1159:Confocal microscopy
987:agent checking the
921:Köhler illumination
707:Fine adjustment (5)
573:Köhler illumination
559:Lighting techniques
292:Confocal microscope
244:Inverted microscope
191:Compound microscope
157:digital microscopes
52:that commonly uses
18:Compound microscope
3439:Optical microscopy
3200:Optical microscopy
3181:Optical microscopy
1626:Digital microscope
1517:
1465:
1337:
1293:numerical aperture
1268:
1205:
1004:
825:
797:numerical aperture
774:Objective (optics)
682:
654:immunofluorescence
538:
534:Francesco Stelluti
514:Christiaan Huygens
439:magnifying glasses
352:Digital microscope
348:
335:Digital microscope
257:optical resolution
201:
144:
42:optical microscope
38:
3416:
3415:
3361:Diffraction limit
2848:10.1117/12.260797
2796:Applied Physics B
2757:10.1117/12.336833
2622:Journal of Optics
2539:Popular Mechanics
2499:978-0-824-74252-2
2361:978-1-55752-910-7
2210:. Harmony Books.
2172:978-0-224-05044-9
2052:Biotechnology 101
2025:978-90-6984-615-6
1961:978-90-6984-615-6
1725:978-0-521-43591-8
1695:978-81-317-6147-2
1659:. msnucleus.org.
1335:
1297:diffraction limit
1212:medical diagnosis
1168:Microspectroscopy
1053:. 1.559 μm/pixel.
1001:stereo microscope
549:Tulane University
461:Zacharias Janssen
421:History of optics
405:entangled photons
385:transillumination
232:Stereo microscope
187:and microscopes.
163:Simple microscope
82:stereo microscope
16:(Redirected from
3446:
3434:Dutch inventions
3404:
3403:
3392:
3391:
3354:limit techniques
3291:
3212:contrast methods
3210:Illumination and
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2530:
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2510:
2504:
2503:
2481:
2475:
2474:
2472:
2470:
2461:. Archived from
2451:
2445:
2444:
2442:
2440:
2431:. Archived from
2421:
2415:
2414:
2399:
2393:
2380:
2374:
2373:
2335:
2329:
2328:
2326:
2324:
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2238:
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2183:
2177:
2176:
2164:
2154:
2148:
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2118:
2116:
2095:
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2080:
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2009:
2003:
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1989:
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1912:
1886:
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1792:
1783:(4): 1169–1193.
1777:Nature Protocols
1768:
1762:
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1730:
1729:
1709:
1700:
1699:
1679:
1673:
1672:
1670:
1668:
1652:
1636:Microscope slide
1605:aluminium alloys
1586:atomic nanoscope
1574:X-ray microscope
1388:evanescent waves
1346:
1344:
1343:
1338:
1336:
1334:
1320:
1227:depth perception
1134:Other techniques
1118:
1099:
1080:
1061:
780:objective lenses
715:Light source (a
696:Objective lenses
608:Georges Nomarski
567:In August 1893,
489:
488:
478:coined the name
450:Cornelis Drebbel
311:light scattering
173:magnifying glass
56:and a system of
46:light microscope
21:
3454:
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3449:
3448:
3447:
3445:
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3443:
3419:
3418:
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3352:Sub-diffraction
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3211:
3205:
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3178:
3114:
3095:
3079:
3077:Further reading
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3026:
3022:
2990:10.1.1.665.3604
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2713:
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2531:
2527:
2512:
2511:
2507:
2500:
2483:
2482:
2478:
2468:
2466:
2453:
2452:
2448:
2438:
2436:
2435:on 15 June 2011
2423:
2422:
2418:
2401:
2400:
2396:
2390:Wayback Machine
2381:
2377:
2362:
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2306:
2305:
2301:
2291:
2289:
2281:
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2246:
2245:
2241:
2230:Q J Microsc Sci
2227:
2226:
2222:
2203:
2199:
2193:Wayback Machine
2184:
2180:
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2011:
2010:
2006:
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1992:
1987:
1978:
1973:
1969:
1962:
1947:
1946:
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1937:
1933:
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1828:(7750): 78–82.
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1640:
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1509:
1501:
1457:
1433:
1417:William Moerner
1411:was awarded to
1372:
1324:
1308:
1307:
1280:resolving power
1257:
1189:
1136:
1129:
1119:
1110:
1100:
1091:
1081:
1072:
1062:
1015:
1009:
993:travel document
974:
957:
929:
901:
874:
868:the condenser.
861:
852:
831:
813:
776:
770:
762:
746:
740:
674:
648:which binds to
624:
561:
526:
471:Galileo Galilei
465:Hans Lippershey
432:
427:
417:
401:photon-counting
373:USB microscopes
354:
337:
307:Ultramicroscope
225:
193:
165:
136:
101:Polarised light
48:, is a type of
28:
23:
22:
15:
12:
11:
5:
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3298:
3294:
3293:
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3284:
3282:
3281:
3276:
3271:
3266:
3261:
3259:4Pi microscope
3256:
3251:
3246:
3241:
3236:
3234:Phase contrast
3231:
3226:
3221:
3215:
3213:
3207:
3206:
3204:
3203:
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3188:
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3184:
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3148:
3147:
3142:
3137:
3131:
3123:
3117:
3108:
3102:
3094:
3093:External links
3091:
3090:
3089:
3083:
3078:
3075:
3074:
3073:
3068:978-9069846156
3067:
3052:
3049:
3047:
3046:
3020:
2966:
2909:
2894:
2861:
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2785:
2770:
2739:
2721:New York Times
2706:
2673:
2647:
2612:
2567:(19): 193905.
2551:
2525:
2505:
2498:
2476:
2446:
2416:
2407:macrolenses.de
2394:
2375:
2360:
2330:
2299:
2287:Microscope.com
2274:
2255:(2): 101–108.
2239:
2220:
2197:
2178:
2171:
2149:
2140:
2131:
2122:
2090:
2081:
2064:
2043:
2031:
2024:
2004:
1990:
1976:
1967:
1960:
1940:
1931:
1871:
1812:
1763:
1731:
1724:
1701:
1694:
1674:
1646:
1644:
1641:
1639:
1638:
1633:
1628:
1622:
1620:
1617:
1609:microstructure
1577:
1576:
1571:
1568:
1562:
1556:
1550:
1544:
1533:
1530:
1508:
1505:
1500:
1497:
1486:light emission
1456:
1453:
1432:
1429:
1371:
1368:
1348:
1347:
1333:
1330:
1327:
1323:
1318:
1315:
1256:
1253:
1216:histopathology
1188:
1185:
1184:
1183:
1180:
1177:
1174:
1171:
1164:
1163:
1162:
1161:
1156:
1148:
1147:
1144:
1135:
1132:
1131:
1130:
1122:Phase contrast
1120:
1113:
1111:
1109:by the sample.
1101:
1094:
1092:
1082:
1075:
1073:
1063:
1056:
1054:
1031:phase contrast
1011:Main article:
1008:
1005:
973:
970:
956:
953:
945:phase contrast
928:
925:
900:
897:
873:
870:
860:
857:
851:
848:
827:Main article:
812:
809:
805:depth of field
772:Main article:
769:
768:Objective lens
766:
761:
758:
742:Main article:
739:
736:
735:
734:
731:
726:Diaphragm and
724:
713:
710:
709:
708:
705:
699:
693:
690:
673:
670:
623:
620:
592:phase contrast
560:
557:
525:
524:Popularization
522:
518:achromatically
476:Giovanni Faber
431:
428:
416:
413:
358:digital camera
350:Main article:
345:USB microscope
336:
333:
332:
331:
317:
304:
301:
295:
289:
283:
277:
271:
261:
260:
250:
247:
241:
235:
224:
221:
217:phase contrast
192:
189:
164:
161:
135:
132:
26:
24:
14:
13:
10:
9:
6:
4:
3:
2:
3451:
3440:
3437:
3435:
3432:
3430:
3427:
3426:
3424:
3409:
3408:
3399:
3397:
3396:
3387:
3386:
3383:
3377:
3374:
3372:
3369:
3367:
3364:
3362:
3359:
3358:
3356:
3350:
3344:
3341:
3339:
3336:
3334:
3331:
3329:
3326:
3323:
3319:
3315:
3312:
3310:
3307:
3305:
3302:
3301:
3299:
3295:
3290:
3280:
3277:
3275:
3272:
3270:
3267:
3265:
3262:
3260:
3257:
3255:
3252:
3250:
3247:
3245:
3242:
3240:
3237:
3235:
3232:
3230:
3227:
3225:
3222:
3220:
3217:
3216:
3214:
3208:
3202:
3201:
3197:
3195:
3194:
3190:
3189:
3186:
3182:
3175:
3170:
3168:
3163:
3161:
3156:
3155:
3152:
3146:
3143:
3141:
3138:
3135:
3132:
3129:
3128:
3124:
3121:
3118:
3112:
3109:
3106:
3103:
3100:
3097:
3096:
3092:
3087:
3084:
3081:
3080:
3076:
3070:
3064:
3060:
3055:
3054:
3051:Cited sources
3050:
3034:
3030:
3024:
3021:
3016:
3012:
3008:
3004:
3000:
2996:
2991:
2986:
2982:
2978:
2970:
2967:
2959:
2955:
2951:
2947:
2943:
2939:
2935:
2932:(6): 927–38.
2931:
2927:
2920:
2913:
2910:
2905:
2898:
2895:
2887:
2883:
2879:
2872:
2865:
2862:
2857:
2853:
2849:
2845:
2841:
2833:
2830:
2825:
2821:
2817:
2813:
2809:
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2762:
2758:
2754:
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2740:
2727:
2723:
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2717:
2710:
2707:
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2648:
2643:
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2613:
2608:
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2562:
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2536:
2529:
2526:
2520:
2515:
2509:
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2501:
2495:
2491:
2487:
2480:
2477:
2464:
2460:
2456:
2450:
2447:
2434:
2430:
2426:
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2417:
2412:
2408:
2404:
2398:
2395:
2391:
2387:
2384:
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2376:
2371:
2367:
2363:
2357:
2353:
2349:
2345:
2341:
2334:
2331:
2318:
2314:
2310:
2303:
2300:
2288:
2284:
2278:
2275:
2270:
2266:
2262:
2258:
2254:
2250:
2243:
2240:
2235:
2231:
2224:
2221:
2217:
2216:0-609-60142-3
2213:
2209:
2208:
2201:
2198:
2194:
2190:
2187:
2182:
2179:
2174:
2168:
2163:
2162:
2153:
2150:
2144:
2141:
2135:
2132:
2126:
2123:
2110:
2106:
2105:
2100:
2094:
2091:
2085:
2082:
2078:
2074:
2068:
2065:
2061:
2057:
2053:
2047:
2044:
2040:
2035:
2032:
2027:
2021:
2017:
2016:
2008:
2005:
1999:
1997:
1995:
1991:
1985:
1983:
1981:
1977:
1971:
1968:
1963:
1957:
1953:
1952:
1944:
1941:
1935:
1932:
1924:
1920:
1916:
1911:
1906:
1902:
1898:
1894:
1890:
1883:
1875:
1872:
1867:
1863:
1859:
1855:
1851:
1847:
1843:
1839:
1835:
1831:
1827:
1823:
1816:
1813:
1808:
1804:
1800:
1796:
1791:
1786:
1782:
1778:
1774:
1767:
1764:
1748:
1741:
1735:
1732:
1727:
1721:
1717:
1716:
1708:
1706:
1702:
1697:
1691:
1687:
1686:
1678:
1675:
1662:
1658:
1655:JR Blueford.
1651:
1648:
1642:
1637:
1634:
1632:
1629:
1627:
1624:
1623:
1618:
1616:
1614:
1610:
1606:
1602:
1601:age hardening
1598:
1593:
1589:
1587:
1581:
1575:
1572:
1569:
1566:
1563:
1560:
1557:
1554:
1551:
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1539:
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1531:
1529:
1526:
1521:
1513:
1506:
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1496:
1494:
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1479:
1474:
1470:
1461:
1454:
1452:
1450:
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1428:
1426:
1422:
1418:
1414:
1410:
1405:
1403:
1398:
1395:
1393:
1389:
1385:
1381:
1376:
1369:
1367:
1365:
1361:
1357:
1353:
1331:
1328:
1325:
1321:
1316:
1313:
1306:
1305:
1304:
1302:
1298:
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1286:
1281:
1277:
1273:
1266:
1261:
1254:
1252:
1249:
1247:
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1238:
1236:
1232:
1228:
1223:
1221:
1217:
1213:
1208:
1202:
1198:
1193:
1186:
1181:
1178:
1175:
1172:
1169:
1166:
1165:
1160:
1157:
1155:
1152:
1151:
1150:
1149:
1145:
1142:
1141:
1140:
1133:
1127:
1123:
1117:
1112:
1108:
1104:
1098:
1093:
1089:
1085:
1079:
1074:
1070:
1066:
1060:
1055:
1052:
1048:
1046:
1044:
1040:
1036:
1032:
1028:
1024:
1020:
1014:
1006:
1002:
998:
994:
990:
986:
983:
978:
971:
969:
966:
962:
961:magnification
955:Magnification
954:
952:
950:
946:
942:
938:
934:
926:
924:
922:
918:
914:
910:
906:
898:
896:
893:
889:
886:
882:
880:
871:
869:
865:
858:
856:
849:
847:
844:
843:immersion oil
840:
836:
830:
829:Oil immersion
822:
821:oil immersion
817:
810:
808:
806:
802:
801:focal lengths
798:
794:
793:magnification
790:
786:
781:
775:
767:
765:
759:
757:
755:
751:
745:
737:
732:
729:
725:
722:
718:
714:
711:
706:
703:
702:
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694:
691:
688:
687:
686:
678:
671:
669:
667:
663:
659:
655:
651:
647:
642:
640:
636:
632:
629:
621:
619:
617:
613:
609:
605:
601:
597:
593:
589:
588:Frits Zernike
585:
580:
578:
574:
570:
569:August Köhler
565:
558:
556:
554:
550:
546:
542:
535:
530:
523:
521:
519:
515:
511:
509:
505:
501:
497:
493:
487:
481:
477:
472:
468:
466:
462:
458:
453:
451:
446:
444:
440:
437:
429:
426:
422:
414:
412:
410:
409:ghost imaging
406:
402:
397:
395:
390:
386:
382:
378:
374:
369:
367:
363:
359:
353:
346:
341:
334:
329:
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321:
318:
316:
312:
308:
305:
302:
299:
296:
293:
290:
287:
284:
281:
278:
275:
272:
269:
266:
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264:
258:
254:
251:
248:
245:
242:
239:
236:
233:
230:
229:
228:
222:
220:
218:
214:
210:
206:
197:
190:
188:
186:
182:
178:
174:
170:
169:virtual image
162:
160:
158:
154:
149:
148:optical power
140:
133:
131:
129:
125:
121:
116:
113:
108:
106:
102:
98:
95:) or around (
94:
89:
87:
83:
79:
75:
70:
68:
64:
59:
55:
54:visible light
51:
47:
43:
34:
30:
19:
3405:
3393:
3322:Three-photon
3199:
3198:
3191:
3126:
3058:
3037:. Retrieved
3023:
2983:(1): 46–54.
2980:
2976:
2969:
2929:
2925:
2912:
2897:
2881:
2877:
2864:
2839:
2832:
2799:
2795:
2788:
2773:
2748:
2742:
2730:. Retrieved
2719:
2709:
2697:. Retrieved
2686:
2676:
2664:. Retrieved
2650:
2625:
2621:
2615:
2564:
2560:
2554:
2542:. Retrieved
2538:
2528:
2517:
2514:"Microscopy"
2508:
2489:
2479:
2467:. Retrieved
2463:the original
2458:
2449:
2437:. Retrieved
2433:the original
2429:company7.com
2428:
2419:
2406:
2397:
2378:
2343:
2333:
2321:. Retrieved
2312:
2302:
2290:. Retrieved
2286:
2277:
2252:
2248:
2242:
2233:
2229:
2223:
2205:
2200:
2181:
2160:
2152:
2143:
2134:
2125:
2113:. Retrieved
2104:Live Science
2102:
2093:
2084:
2067:
2051:
2046:
2034:
2014:
2007:
1970:
1950:
1943:
1934:
1895:(12): 1049.
1892:
1888:
1874:
1825:
1821:
1815:
1780:
1776:
1766:
1754:. Retrieved
1734:
1714:
1684:
1677:
1665:. Retrieved
1650:
1594:
1590:
1582:
1578:
1535:
1532:Alternatives
1518:
1502:
1490:
1466:
1434:
1406:
1399:
1396:
1377:
1373:
1363:
1359:
1354:light. With
1349:
1300:
1279:
1269:
1250:
1239:
1224:
1209:
1206:
1187:Applications
1137:
1126:interference
1065:Bright field
1051:tissue paper
1016:
989:authenticity
958:
930:
909:halogen lamp
902:
899:Light source
894:
890:
887:
883:
875:
866:
862:
853:
832:
777:
763:
756:objectives.
754:apochromatic
747:
683:
643:
625:
616:interference
598:rather than
596:interference
581:
566:
562:
539:
512:
507:
503:
495:
491:
479:
469:
454:
447:
433:
398:
370:
366:histological
355:
343:A miniature
262:
226:
202:
166:
145:
117:
109:
93:bright field
90:
73:
71:
45:
41:
39:
29:
3429:Microscopes
3140:OpenWetWare
3115:(in German)
3039:24 February
2884:: 252–253.
2878:Cell Vision
2802:(1): 1–12.
2666:25 February
1525:Stefan Hell
1421:Stefan Hell
1413:Eric Betzig
1386:which uses
1380:Vertico SMI
1272:diffraction
1255:Limitations
1220:smear tests
1041:) combines
850:Focus knobs
628:fluorescent
584:Nobel Prize
110:A range of
65:and sample
3423:Categories
3318:Two-photon
3193:Microscope
2628:(3): 125.
2544:3 November
2486:"Reticles"
2323:29 October
2292:8 February
2249:J Hist Med
2077:Van Helden
2073:Van Helden
2060:0313335281
2039:Van Helden
1756:5 November
1667:15 January
1643:References
1449:wavelength
1441:microscope
1375:analysis.
1285:wavelength
1276:Airy disks
1265:Ernst Abbe
1246:crosshairs
1231:eye strain
1197:smear test
1103:Dark field
1069:absorbance
1027:dark field
1013:Microscopy
941:dark field
819:Two Leica
672:Components
658:antibodies
639:wavelength
600:absorption
571:developed
496:little eye
492:occhiolino
480:microscope
443:eyeglasses
419:See also:
381:macro lens
209:real image
185:telescopes
97:dark field
86:micrograph
63:resolution
50:microscope
2985:CiteSeerX
2765:128763403
2732:8 October
2699:8 October
2574:1103.3643
2079:, p. 43).
1919:2334-2536
1850:1476-4687
1799:1750-2799
1607:, or the
1482:molecules
1322:λ
1201:wet mount
1107:scattered
1088:polarized
972:Operation
937:diaphragm
933:condenser
927:Condenser
728:condenser
604:mammalian
577:lightbulb
430:Invention
205:objective
181:eyepieces
112:objective
78:eyepieces
3395:Category
3033:Archived
3007:21118230
2958:Archived
2954:18162278
2946:19548231
2886:Archived
2856:55468495
2824:13805053
2726:Archived
2693:Archived
2660:Archived
2607:15793849
2599:21668161
2411:Archived
2386:Archived
2370:13366261
2317:Archived
2236:: 18–24.
2189:Archived
2115:31 March
2109:Archived
1923:Archived
1866:92998248
1858:30944493
1807:30911174
1747:Archived
1661:Archived
1619:See also
1613:polymers
1478:diameter
1445:distance
1019:contrast
999:using a
968:1,000x.
965:eyepiece
841:such as
785:parfocal
750:eyepiece
744:Eyepiece
362:computer
213:eyepiece
153:research
67:contrast
3407:Commons
3015:2119158
2804:Bibcode
2688:AP News
2630:Bibcode
2579:Bibcode
2469:11 July
2439:11 July
2269:4572620
2041:, p. 43
1897:Bibcode
1830:Bibcode
1242:reticle
666:express
553:cholera
508:σκοπεῖν
415:History
377:webcams
368:stain.
3269:Sarfus
3065:
3013:
3005:
2987:
2952:
2944:
2854:
2822:
2763:
2605:
2597:
2519:&c
2496:
2368:
2358:
2267:
2214:
2169:
2058:
2022:
1958:
1917:
1889:Optica
1864:
1856:
1848:
1822:Nature
1805:
1797:
1722:
1692:
1555:(SICM)
1402:sarfus
1390:, and
1278:. The
1235:window
1039:Sarfus
995:at an
917:lasers
905:mirror
879:slides
721:mirror
631:probes
536:, 1630
504:μικρόν
502:words
494:" or "
179:, and
177:loupes
58:lenses
3279:Raman
3011:S2CID
2961:(PDF)
2950:S2CID
2922:(PDF)
2889:(PDF)
2874:(PDF)
2852:S2CID
2820:S2CID
2761:S2CID
2603:S2CID
2569:arXiv
2366:S2CID
1926:(PDF)
1885:(PDF)
1862:S2CID
1750:(PDF)
1743:(PDF)
1567:(TEM)
1561:(STM)
1549:(SEM)
1543:(AFM)
1352:green
1289:light
991:of a
980:U.S.
872:Stage
859:Frame
789:focus
723:) (7)
719:or a
717:light
500:Greek
457:Dutch
134:Types
74:stage
3063:ISBN
3041:2009
3003:PMID
2942:PMID
2734:2014
2701:2014
2668:2009
2595:PMID
2546:2020
2494:ISBN
2471:2011
2441:2011
2356:ISBN
2325:2008
2294:2023
2265:PMID
2212:ISBN
2167:ISBN
2117:2017
2056:ISBN
2020:ISBN
1956:ISBN
1915:ISSN
1854:PMID
1846:ISSN
1803:PMID
1795:ISSN
1758:2015
1720:ISBN
1690:ISBN
1669:2017
1507:STED
1419:and
1033:and
947:and
931:The
915:and
913:LEDs
795:and
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