By Arvid B. Maunsbach, Björn A. Afzelius
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Extra info for Biomedical Electron Microscopy. Illustrated Methods and Interpretations
1C A rat liver fixed for 2 hr in 2% glutaraldehyde in the same buffer solution as in Fig. 1 M phosphate buffer for 2 hr. Embedding and staining as in Fig. 1A. • 25,000. By comparing "single" and "double-fixed" tissues the impression is gained that double fixation retains more material in the mitochondrial matrix and in the cytoplasmic ground substance. This impression is supported by studies that show a greater extraction of lipids and proteins in tissues fixed in osmium tetroxide alone as compared to glutaraldehyde followed by osmium tetroxide.
Electron Microsc. Tech. 6, 255-301. Fawcett, D. W. " Saunders, Philadelphia. Harb, J. M. (1993). Interpretation of TEM micrographs for human diagnosis. Microsc. Soc. Am. Bull 23, 206-218. Hockley, D. , Wood, R. , Jacobs, J. , and Garrett, A. J. (1988). Electron microscopy of human immunodeficiency virus. J. Gen. Virol. 69, 2455-2469. Johannessen, J. V. (1977). Use of paraffin material for electron microscopy. Pathol. Annu. 12, 189-224. JCrgensen, P. L. (1974). Purification and characterization of (Na+-K+) ATPase.
One reason why a 10% formalin solution (which contains 4% formaldehyde) is a less than optimal fixative for electron microscopy is that it contains formic acid and other impurities and that it often does not contain solutes that protect cells from osmotic distortions. A better result can be expected from a buffered and osmotically balanced formaldehyde solution. In Figs. 14C the cell originates from an adrenal tumor, and the question was whether the tumor is a pheochromocytoma from the adrenal medulla or a cancer of the adrenal cortex.