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POLYESTER-METHACRYLATE EMBEDMENTS FOR ELECTRON MICROSCOPY

It has been found that tissues fixed for electron microscopy and dehydrated in acetone can be embedded in mixtures of n-butyl methacrylate and polyester resin. Activation with 1 per cent tert-butyl hydroperoxide followed by 12 to 48 hours at 60°C produces blocks that section well with glass knives....

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Detalles Bibliográficos
Autores principales: Low, Frank N., Clevenger, Max R.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1962
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2106052/
https://www.ncbi.nlm.nih.gov/pubmed/14466917
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author Low, Frank N.
Clevenger, Max R.
author_facet Low, Frank N.
Clevenger, Max R.
author_sort Low, Frank N.
collection PubMed
description It has been found that tissues fixed for electron microscopy and dehydrated in acetone can be embedded in mixtures of n-butyl methacrylate and polyester resin. Activation with 1 per cent tert-butyl hydroperoxide followed by 12 to 48 hours at 60°C produces blocks that section well with glass knives. The ribbons are cleared of methacrylate by heat (200–250°C for 1 hour) and/or immersion in organic solvents (CCL(4), acetone-ether). After removal of the methacrylate the residual polyester matrix provides thermostable and insoluble support for the tissue. Its insolubility permits staining by immersion of cleared preparations in organic solvents carrying heavy metal compounds in solution. Clearing by heat stabilizes section-grid relationships. The removal of volatile materials by clearing substantially reduces contamination of both specimen and microscope. Tissue fine structure is well preserved in these preparations.
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spelling pubmed-21060522008-05-01 POLYESTER-METHACRYLATE EMBEDMENTS FOR ELECTRON MICROSCOPY Low, Frank N. Clevenger, Max R. J Cell Biol Article It has been found that tissues fixed for electron microscopy and dehydrated in acetone can be embedded in mixtures of n-butyl methacrylate and polyester resin. Activation with 1 per cent tert-butyl hydroperoxide followed by 12 to 48 hours at 60°C produces blocks that section well with glass knives. The ribbons are cleared of methacrylate by heat (200–250°C for 1 hour) and/or immersion in organic solvents (CCL(4), acetone-ether). After removal of the methacrylate the residual polyester matrix provides thermostable and insoluble support for the tissue. Its insolubility permits staining by immersion of cleared preparations in organic solvents carrying heavy metal compounds in solution. Clearing by heat stabilizes section-grid relationships. The removal of volatile materials by clearing substantially reduces contamination of both specimen and microscope. Tissue fine structure is well preserved in these preparations. The Rockefeller University Press 1962-03-01 /pmc/articles/PMC2106052/ /pubmed/14466917 Text en Copyright © Copyright, 1962, by The Rockefeller Institute Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Low, Frank N.
Clevenger, Max R.
POLYESTER-METHACRYLATE EMBEDMENTS FOR ELECTRON MICROSCOPY
title POLYESTER-METHACRYLATE EMBEDMENTS FOR ELECTRON MICROSCOPY
title_full POLYESTER-METHACRYLATE EMBEDMENTS FOR ELECTRON MICROSCOPY
title_fullStr POLYESTER-METHACRYLATE EMBEDMENTS FOR ELECTRON MICROSCOPY
title_full_unstemmed POLYESTER-METHACRYLATE EMBEDMENTS FOR ELECTRON MICROSCOPY
title_short POLYESTER-METHACRYLATE EMBEDMENTS FOR ELECTRON MICROSCOPY
title_sort polyester-methacrylate embedments for electron microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2106052/
https://www.ncbi.nlm.nih.gov/pubmed/14466917
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AT clevengermaxr polyestermethacrylateembedmentsforelectronmicroscopy