Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1982 Sep;14(5):823-35.
doi: 10.1007/BF01033631.

Imidazole-buffered osmium tetroxide: an excellent stain for visualization of lipids in transmission electron microscopy

Imidazole-buffered osmium tetroxide: an excellent stain for visualization of lipids in transmission electron microscopy

S Angermüller et al. Histochem J. 1982 Sep.

Abstract

The usefulness of imidazole-buffered osmium tetroxide as a stain for lipids in transmission electron microscopy has been investigated. Rat liver and other tissues were fixed by perfusion with glutaraldehyde and post-fixed with osmium-imidazole and the appearance of lipid droplets was compared with that after post-fixation in unbuffered aqueous osmium tetroxide or an osmium solution buffered otherwise. Prominent electron-opaque staining of lipid droplets and of lipoprotein particles was noted after post-fixation with 2% osmium-imidazole, pH 7.5, for 30 min. The lipid droplets appeared well circumscribed with no evidence of diffusion. In contrast, the intensity of staining was much less and there was some diffusion around lipid droplets in material post-fixed in aqueous or cacodylate-buffered osmium tetroxide. Spot tests on filter paper revealed that unsaturated fatty acids, especially linolenic and linoleic acids reacted more intensely with osmium-imidazole than with aqueous osmium tetroxide. These findings demonstrate that osmium-imidazole provides an excellent stain for lipids in transmission electron microscopy and that most probably it stains lipids with unsaturated fatty acids.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Am J Anat. 1971 Dec;132(4):429-62 - PubMed
    1. Physiol Rev. 1976 Apr;56(2):259-316 - PubMed
    1. J Histochem Cytochem. 1980 Jul;28(7):645-52 - PubMed
    1. J Invest Dermatol. 1981 Jun;76(6):438-41 - PubMed
    1. Adv Enzymol Relat Subj Biochem. 1958;20:51-110 - PubMed

Publication types