| DK | dark; decay; diabetic ketoacidosis; diet kitchen; diseased kidney; dog kidney [cells] |
|---|---|
| FADF | fluorescent antibody dark field |
| SNRT | Sinus Node Recovery Time |
| ART | absolute retention time; Accredited Record Technician; acoustic reflex test; algebraic reconstructio... |
| BR | barrier reared [experimental animals]; baseline recovery; bathroom; bed rest; bedside rounds; biliru... |
| fluorescence recovery after photobleaching | Many fluorochromes are bleached by exposure to exciting light. If, for example: the cell surface is labelled with a fluorescent probe and an area bleached by laser illumination, then the bleached patch that starts off as a dark area will gradually recover fluorescence. The recovery is due to the re population of the area by unbleached molecules and diffusion of bleached molecules to other areas. The rate and extent of recovery are a measure of the fluidity of the membrane and the proportion of labelled molecules that are free to exchange with adjacent areas. The technique is usually applied to cell surface fluidity or viscosity measurements, but is also applicable to other structures. (18 Nov 1997) |
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| cardioid dark field condenser | <microscopy> A condenser designed with two reflecting surfaces, the first, a spherical surface which reflects the rays to a second, cardioid (heart-shaped) surface. The virtue in such an arrangement is that, if the cardioid surface is of true figure, the lens is both achromatic and aplanatic. It has a limiting numerical aperture of about 1.0. Thus objectives of a greater numerical aperture cannot be used successfully with it. A true cardioid figure is the trace of a point on the circumference of a circle rolling around an equal, fixed circle. (05 Aug 1998) |
| paraboloid dark field condenser | <microscopy> A lens of parabolic shape. The vertex end is ground back so that its focus can be brought into coincidence with the specimen on the slide. A central stop is provided to block the central rays. It is used chiefly for medium- power work. (05 Aug 1998) |
| condenser, dark field | <microscopy> A condenser forming a hollow cone of light with its apex (or focal point) in the plane of the specimen. When used with an objective having a numerical aperture lower than the minimum numerical aperture of the hollow cone, only light deviated by the specimen enters the objective. Objects are seen as bright images against a dark background. The ordinary bright field condenser of low power, used with a central stop, makes a good dark field condenser. They all form a dark field while illuminating the specimen with a hollow cone of light. The lower limiting aperture of the condenser must be greater than the numerical aperture of the objective with which it is to be used. Thus, no direct light enters the objective, the specimen is seen by reflected or scattered light on a dark background. See: condensers See: special dark field condensers: paraboloid, cardioid and Cassegrainian. (05 Aug 1998) |
| dark adaptation | The adjustment of the eye occurring under reduced illumination in which the sensitivity to light is greatly increased or the light threshold is greatly reduced. Dark adaptation is slower than light adaptation. During dark adaptation rhodopsin is built up in the retinal rods. (12 Dec 1998) |
| dark-adapted eye | An eye that has been in darkness or semidarkness and has undergone regeneration of rhodopsin (visual purple), which renders it more sensitive to reduced illumination. Synonym: scotopic eye. (05 Mar 2000) |
| dark cell | Cell's in eccrine sweat glands having many ribosomes and mucoid secretory granules. (05 Mar 2000) |
| dark current | <physiology> Current caused by constant influx of sodium ions into the rod outer segment of retinal photoreceptors and that is blocked by light (leading to hyperpolarization). The plasma membrane sodium channel is controlled through a cascade of amplification reactions initiated by photon capture by rhodopsin in the disc membrane. (18 Nov 1997) |
| dark-field condenser | An apparatus for throwing reflected light through the microscope field, so that only the object to be examined is illuminated, the field itself being dark. (05 Mar 2000) |
| dark field illumination | <microscopy> Any method of illumination which illuminates the specimen but does not admit light directly to the objective. It may be by substage (dark field) condensers, by stagespot lighting, by special condensers fitted around special objectives for reflected illumination or by the slit ultramicroscope. (05 Aug 1998) |
| dark field imaging | <microscopy> Using a single diffracted beam to form the image in a transmission electron microscope. This causes all regions of the specimen not of the same crystal structure and orientation as the region which produced the diffracted beam to be represented as very dark in the final image, allowing phase differentiation visually in the transmission electron microscope. (05 Aug 1998) |
| dark-field microscope | <instrument> A microscope that has a special condenser and objective with a diaphragm or stop that scatters light from the object observed, with the result that the object appears bright on a dark background. (05 Mar 2000) |
| dark field microscopy | <procedure> A system of microscopy in which particles are illuminated at a very low angle from the side so that the background appears dark and the objects are seen by diffracted and reflected patches of light against a dark background. (18 Nov 1997) |
| dark field objective | <microscopy> Certain objectives for high-power, dark fieldwork equipped with iris diaphragms or funnel stops so that their apertures may be reduced to correspond to the dark field con-denser with which they are used. (05 Aug 1998) |
| dark field slides | <microscopy> Owing to the exacting demands of dark field illumination, not only must the microscope slide be especially clean, but also the glass of which the slide is composed must be optically clear under dark field conditions. The glass should not fluoresce. (05 Aug 1998) |