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The Journal of Biophysical and Biochemical Cytology logoLink to The Journal of Biophysical and Biochemical Cytology
. 1960 Feb 1;7(1):27–30. doi: 10.1083/jcb.7.1.27

Epoxy Resins in Electron Microscopy

Henry Finck 1
PMCID: PMC2224867  PMID: 13822825

Abstract

A method of embedding biological specimens in araldite 502 (Ciba) has been developed for materials available in the United States. Araldite-embedded tissues are suitable for electron microscopy, but the cutting qualities of the resin necessitates more than routine attention during microtomy. The rather high viscosity of araldite 502 also seems to be an unnecessary handicap. The less viscous epoxy epon 812 (Shell) produces specimens with improved cutting qualities, and has several features—low shrinkage and absence of specimen damage during cure, minimal compression of sections, relative absence of electron beam-induced section damage, etc.—which recommends it as a routine embedding material. The hardness of the cured resin can be easily adjusted by several methods to suit the materials embedded in it. Several problems and advantages of working with sections of epoxy resins are also discussed.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. GLAUERT A. M., GLAUERT R. H. Araldite as an embedding medium for electron microscopy. J Biophys Biochem Cytol. 1958 Mar 25;4(2):191–194. doi: 10.1083/jcb.4.2.191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. GLAUERT A. M., GLAUERT R. H., ROGERS G. E. A new embedding medium for electron microscopy. Nature. 1956 Oct 13;178(4537):803–803. doi: 10.1038/178803a0. [DOI] [PubMed] [Google Scholar]
  3. MOORE D. H., GRIMLEY P. H. Problems in methacrylate embedding for electron microscopy. J Biophys Biochem Cytol. 1957 Mar 25;3(2):255–260. doi: 10.1083/jcb.3.2.255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. ROBERTSON J. D. Structural alterations in nerve fibers produced by hypotonic and hypertonic solutions. J Biophys Biochem Cytol. 1958 Jul 25;4(4):349–364. doi: 10.1083/jcb.4.4.349. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. SATIR P. G., PEACHEY L. D. Thin sections. II. A simple method for reducing compression artifacts. J Biophys Biochem Cytol. 1958 May 25;4(3):345–348. doi: 10.1083/jcb.4.3.345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. SOTELO J. R. Technical improvements in specimen preparation for electron microscopy. Exp Cell Res. 1957 Dec;13(3):599–601. doi: 10.1016/0014-4827(57)90091-5. [DOI] [PubMed] [Google Scholar]
  7. WATSON M. L. Staining of tissue sections for electron microscopy with heavy metals. J Biophys Biochem Cytol. 1958 Jul 25;4(4):475–478. doi: 10.1083/jcb.4.4.475. [DOI] [PMC free article] [PubMed] [Google Scholar]

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