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SILVER IMPREGNATION OF ULTRATHIN SECTIONS FOR ELECTRON MICROSCOPY

A new procedure is described for silver impregnation of thin sections for electron microscopy. Sections of various tissues, fixed in OsO(4) and embedded in methacrylate, were treated with an ammoniacal silver solution, directly or after oxidation with periodic acid or hydrogen peroxide. After OsO(4)...

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Detalles Bibliográficos
Autor principal: Marinozzi, Vittorio
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1961
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2224991/
https://www.ncbi.nlm.nih.gov/pubmed/13766855
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author Marinozzi, Vittorio
author_facet Marinozzi, Vittorio
author_sort Marinozzi, Vittorio
collection PubMed
description A new procedure is described for silver impregnation of thin sections for electron microscopy. Sections of various tissues, fixed in OsO(4) and embedded in methacrylate, were treated with an ammoniacal silver solution, directly or after oxidation with periodic acid or hydrogen peroxide. After OsO(4) fixation all cellular membranous systems exhibit a primary argentaffinity probably due to the reduction of ammoniacal silver solution by the reduced osmium bound to unsaturated lipids. Bleaching the sections with hydrogen peroxide removes the argentaffinity of protoplasmic structures. Treatment of the sections with periodic acid results in decreased argentaffinity of protoplasmic components while the argentaffinity of metaplasmic structures is greatly enhanced. The latter procedure appears particularly useful for enhancing the contrast of basement membranes.
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spelling pubmed-22249912008-05-01 SILVER IMPREGNATION OF ULTRATHIN SECTIONS FOR ELECTRON MICROSCOPY Marinozzi, Vittorio J Biophys Biochem Cytol Article A new procedure is described for silver impregnation of thin sections for electron microscopy. Sections of various tissues, fixed in OsO(4) and embedded in methacrylate, were treated with an ammoniacal silver solution, directly or after oxidation with periodic acid or hydrogen peroxide. After OsO(4) fixation all cellular membranous systems exhibit a primary argentaffinity probably due to the reduction of ammoniacal silver solution by the reduced osmium bound to unsaturated lipids. Bleaching the sections with hydrogen peroxide removes the argentaffinity of protoplasmic structures. Treatment of the sections with periodic acid results in decreased argentaffinity of protoplasmic components while the argentaffinity of metaplasmic structures is greatly enhanced. The latter procedure appears particularly useful for enhancing the contrast of basement membranes. The Rockefeller University Press 1961-01-01 /pmc/articles/PMC2224991/ /pubmed/13766855 Text en Copyright © Copyright, 1961, by The Rockefeller Institute Press
spellingShingle Article
Marinozzi, Vittorio
SILVER IMPREGNATION OF ULTRATHIN SECTIONS FOR ELECTRON MICROSCOPY
title SILVER IMPREGNATION OF ULTRATHIN SECTIONS FOR ELECTRON MICROSCOPY
title_full SILVER IMPREGNATION OF ULTRATHIN SECTIONS FOR ELECTRON MICROSCOPY
title_fullStr SILVER IMPREGNATION OF ULTRATHIN SECTIONS FOR ELECTRON MICROSCOPY
title_full_unstemmed SILVER IMPREGNATION OF ULTRATHIN SECTIONS FOR ELECTRON MICROSCOPY
title_short SILVER IMPREGNATION OF ULTRATHIN SECTIONS FOR ELECTRON MICROSCOPY
title_sort silver impregnation of ultrathin sections for electron microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2224991/
https://www.ncbi.nlm.nih.gov/pubmed/13766855
work_keys_str_mv AT marinozzivittorio silverimpregnationofultrathinsectionsforelectronmicroscopy