A new epoxy embedding mixture has been developed utilizing Maraglas 655 and Cardolite NC-513 with benzyldimethylamine (BDMA) as a curing agent. This epoxy mixture permits cellular preservation comparable to that obtained with Epon 812, ease of preparation of tissues, a wide range of miscibility, low viscosity, and, most important, ease of sectioning on a Porter-Blum microtome. In contrast to Epon-812-embedded tissues, Maraglas-Cardolite-embedded tissues can be sectioned in large dimensions with ease and consistent results without "chatter." No background granularity is detectable with high magnification study of Maraglas-Cardolite-embedded tissues. This epoxy is readily stained with lead hydroxide and is relatively stable in the electron beam.
Skip Nav Destination
Article navigation
1 June 1962
Article|
June 01 1962
A NEW EPOXY EMBEDMENT FOR ELECTRON MICROSCOPY
James A. Freeman,
James A. Freeman
From the Department of Pathology, Louisiana State University School of Medicine, New Orleans
Search for other works by this author on:
Ben O. Spurlock
Ben O. Spurlock
From the Department of Pathology, Louisiana State University School of Medicine, New Orleans
Search for other works by this author on:
James A. Freeman
From the Department of Pathology, Louisiana State University School of Medicine, New Orleans
Ben O. Spurlock
From the Department of Pathology, Louisiana State University School of Medicine, New Orleans
Received:
January 30 1962
Online ISSN: 1540-8140
Print ISSN: 0021-9525
Copyright © 1962 by The Rockefeller Institute Press
1962
J Cell Biol (1962) 13 (3): 437–443.
Article history
Received:
January 30 1962
Citation
James A. Freeman, Ben O. Spurlock; A NEW EPOXY EMBEDMENT FOR ELECTRON MICROSCOPY . J Cell Biol 1 June 1962; 13 (3): 437–443. doi: https://doi.org/10.1083/jcb.13.3.437
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 InstitutionEmail alerts
Advertisement
Advertisement