Modern microscopists have developed a wide spectrum of useful techniques designed to aid in contrast enhancement and provide better observation and photomicrography of specimens. This section of the Microscopy Primer describes many of these techniques in detail.
With the assistance of Dr. Robert Hoffman, we review the problems of contrast enhancement with both amplitude and phase specimens and review techniques that have been developed to assist with specimen contrast.
The following section discusses various aspects of the theory and practice of condenser design and other important concepts in both transmitted and reflected light darkfield microscopy.
A mechanism for rendering contrast in transparent specimens, differential interference contrast (DIC) microscopy is a beam-shearing interference system in which the reference beam is sheared by a tiny amount.
Learn more about Hoffman Modulation Contrast which was invented by Dr. Robert Hoffman. This contrast-enhancing technique serves to increase specimen visibility and contrast, especially for unstained and living specimens.
Achieving conditions for oblique illumination, which has been employed to enhance specimen visibility since the dawn of microscopy, can be accomplished by a variety of techniques with a simple transmitted optical microscope.
Phase contrast provides an excellent method of improving contrast in unstained biological specimens without significant loss in resolution, and is widely utilized to examine is widely utilized from inspection of cultured cell to examination of dynamic events in living cells.
Polarized Light Microscopy exploits optical properties of anisotropy to reveal detailed information about the structure and composition of materials, which are invaluable for identification and diagnostic purposes.
First described around the turn of the century by British microscopist Julius Rheinberg, this technique provides beautiful high-contrast colored images of unstained specimens.
Confocal microscopy offers the ability to control depth of field, elimination or reduction of background information away from the focal plane, and the capability to collect serial optical sections from thick specimens.
The range of applications available to Laser Scanning Confocal Microscopy include a variety of studies in neuroanatomy, neurophysiology, as well as morphological studies of a wide spectrum of cells and tissues.
Learn all about laser scanning microscopes, including their advantages, disadvantages, and the types of images they can produce.
For ultra-high optical resolution, near-field scanning optical microscopy (NSOM) is currently the photonic instrument of choice. Near-field imaging occurs when a sub-micron optical probe is positioned a very short distance from the sample and light is transmitted through a small aperture at the tip of this probe.
Fluorescence illumination is the most rapidly expanding microscopy technique employed today, both in the medical and biological sciences, a fact which has spurred the development of more sophisticated microscopes.
Fluorescence microscopy can be combined with contrast enhancing techniques such as DIC illumination to minimize the effects of photobleaching by locating a specific area of interest in a specimen using DIC.
Fluorescence microscopy can be combined with phase contrast to minimize the effects of photobleaching by locating a specific area of interest in a specimen using phase contrast.
Discover and explore this gallery of featured interactive java tutorials/applets designed to aid students in understanding difficult concepts in various specialized microscopy techniques.
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