. Cytology. Cytology. Ultraviolet protecting filter (Leitz #8574A) _^SIide J Ultraviolet filter (Corning #584t428) Mecury lamp. Figure 11-29. Schematic Diagram Showing the Arrangement of Micro- scopic Components for the Study of Ceils and Tissues by Fluorescent Light. (From Popper, H. and Szanto, P. B., 1950. "Fluorescence Microscopy," in Jones, R. M. (Ed.), "McClung's Handbook of Microscopical Technique," 3rd ed., Paul B. Hoeber, Inc., Harper & Brothers. New York, N. Y., Fig. 130, p. 679.) ard microscope lenses can be used. The method most often employed in fluorescenc
. Cytology. Cytology. Ultraviolet protecting filter (Leitz #8574A) _^SIide J Ultraviolet filter (Corning #584t428) Mecury lamp. Figure 11-29. Schematic Diagram Showing the Arrangement of Micro- scopic Components for the Study of Ceils and Tissues by Fluorescent Light. (From Popper, H. and Szanto, P. B., 1950. "Fluorescence Microscopy," in Jones, R. M. (Ed.), "McClung's Handbook of Microscopical Technique," 3rd ed., Paul B. Hoeber, Inc., Harper & Brothers. New York, N. Y., Fig. 130, p. 679.) ard microscope lenses can be used. The method most often employed in fluorescence microscopy is the crossed filter technique (Figure 11-29). A source filter that transmits only the ultraviolet radiation to be absorbed by the specimen is positioned in front of the light source (mercury vapor or carbon arc lamp). A complementary filter is mounted in the eyepiece or body tube of the microscope for visual observation and photography. SURVEY OF CYTOLOGICAL TECHNIQUES / 251. Please note that these images are extracted from scanned page images that may have been digitally enhanced for readability - coloration and appearance of these illustrations may not perfectly resemble the original Wilson, G. B. (George Bernard), 1914-; Morrison, John H. (John Herbert), 1927-. New York, Reinhold
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