After aldehyde-fixation, treatment with phosphotungstic acid (PTA) in aqueous acidic medium was shown to produce an intense electron-opaque stain with minimal distortion of organelles. Mitochondrial matrix, cisternae of the endoplasmic reticulum, and the Z-band of muscle were densely stained, whereas membranes stood out in negative contrast. Staining of glycogen or lipid was not apparent. Under certain conditions the stain density reflected the concentration of protein based on the quantitative reaction of PTA with the positively charged groups, although the stoichiometry of the reaction between PTA and protein varied with the kind of protein. The staining conditions established should provide a base for the use of the method in quantitative electron microscopy, particularly on thin sections.
Skip Nav Destination
Article navigation
1 March 1969
Article|
March 01 1969
THE REACTIVITY AND STAINING OF TISSUE PROTEINS WITH PHOSPHOTUNGSTIC ACID
Lloyd Silverman,
Lloyd Silverman
From the Division of Histochemistry, Department of Pathology, Stanford University Medical School, Palo Alto, California 94304
Search for other works by this author on:
David Glick
David Glick
From the Division of Histochemistry, Department of Pathology, Stanford University Medical School, Palo Alto, California 94304
Search for other works by this author on:
Lloyd Silverman
From the Division of Histochemistry, Department of Pathology, Stanford University Medical School, Palo Alto, California 94304
David Glick
From the Division of Histochemistry, Department of Pathology, Stanford University Medical School, Palo Alto, California 94304
Received:
June 24 1968
Online ISSN: 1540-8140
Print ISSN: 0021-9525
Copyright © 1969 by The Rockefeller University Press.
1969
J Cell Biol (1969) 40 (3): 761–767.
Article history
Received:
June 24 1968
Citation
Lloyd Silverman, David Glick; THE REACTIVITY AND STAINING OF TISSUE PROTEINS WITH PHOSPHOTUNGSTIC ACID . J Cell Biol 1 March 1969; 40 (3): 761–767. doi: https://doi.org/10.1083/jcb.40.3.761
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement
Advertisement