A simple method for the preparation of cell cultures for ultrastructural investigation.
Open Access
- 1 January 1981
- journal article
- research article
- Published by SAGE Publications in Journal of Histochemistry & Cytochemistry
- Vol. 29 (1) , 84-86
- https://doi.org/10.1177/29.1.7009731
Abstract
A method is described that allows investigation of cultured cells at the light or electron microscopical level without changing the culturing conditions or the in situ situation during dehydration or embedding. Fixed and dehydrated cell culture layers were cut into small pieces and separated from the plastic dish by adding propylene oxide. With this simple method we could obtain orientated sections of selected cell groups.This publication has 7 references indexed in Scilit:
- Interaction of leukocytes with vascular cells in cultureJournal of Cell Science, 1978
- Direct Epoxy Embedding for Vertical Sectioning of Cells Grown as a Monolayer on Millipore FilterStain Technology, 1968
- PROCEDURE FOR EMBEDDING IN SITU SELECTED CELLS CULTURED IN VITROThe Journal of cell biology, 1967
- Polyester Sheeting (Melinex O), a Tissue-Culture Support Easily Separable from Epoxy Resins after Flat-Face EmbeddingStain Technology, 1966
- FIBROBLASTS IN TISSUE CULTURE - USE OF COLLOIDAL IRON FOR ULTRASTRUCTURAL LOCALIZATION OF ACID MUCOPOLYSACCHARIDES1965
- Sandwich Embedding of Monolayers of Cells in Epoxy Resin for Ultrathin SectioningStain Technology, 1965
- Open-Face, Epoxy Embedding of Single Cells for Ultrathin SectionsStain Technology, 1965