Light microscopic localization of cytochemical reactions in epoxy-embedded material for electron microscopy.
Author(s) -
J. Russo,
Peter A. Wells
Publication year - 1975
Publication title -
journal of histochemistry and cytochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.971
H-Index - 124
eISSN - 1551-5044
pISSN - 0022-1554
DOI - 10.1177/23.12.127811
Subject(s) - electron microscope , osmium tetroxide , glutaraldehyde , microscopy , scanning electron microscope , phase contrast microscopy , chemistry , osmium , microscope , ultrastructure , cytochemistry , toluidine , materials science , pathology , anatomy , enzyme , optics , biochemistry , biology , chromatography , catalysis , medicine , physics , ruthenium , composite material
Tissues from mice were fixed in 1.5% glutaraldehyde, treated for the ultrastructural localization of alkaline phosphatase or Mg++-dependent adenosine triphosphatase, post-fixed in osmium tetroxide, dehydrated and embedded in plastic for electron microscopy. The sites of reaction were visualized in 1-mu plastic sections counterstained with toluidine blue, using a phase contrast microscope. The data show a close correlation between the sites of reaction observed with the phase contrast microscope and the sites studied with the electron microscope. The use of this technique for the study of these phosphatases in normal and pathologic tissues is recommended in order to achieve a high degree of accuracy in selecting a portion of the tissue sample for electron microscopy and to obtain greater resolution in the localization of these enzymes with the light microscope.
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