Progression Of Fusion During Rapid Freezing For Electron Microscopy
- 1 April 1979
- journal article
- Published by Wiley in Journal of Microscopy
- Vol. 115 (3), 243-256
- https://doi.org/10.1111/j.1365-2818.1979.tb00176.x
Abstract
The method used to determine the rate of fusion was based on the large difference in the dielectric constants of water and ice. A thin (50–60 μm) slice of a gelatin gel was used as the dielectric in a plate condenser. The slice was placed on a metal electrode built in a specimen carrier which was dropped on a silver freezing surface kept at below 70 K, forming the other plate of the condenser. Freezing of the gelatin causes a marked decrease in a 20,000 cycle current passing through the condenser. Since the thickness of the layer of frozen material was shown to be a function of the reciprocal of the current, it was possible to determine the course of fusion of the section. Freezing started at a high rate which declined during the first 5 ms but then increased again and usually became quite high at the end of fusion.Keywords
This publication has 8 references indexed in Scilit:
- Synaptic vesicle exocytosis captured by quick freezing and correlated with quantal transmitter release.The Journal of cell biology, 1979
- Preservation of Synaptic Structure by Rapid FreezingCold Spring Harbor Symposia on Quantitative Biology, 1976
- Synaptic changes in frog brain after stimulation with potassium chlorideJournal of Neurocytology, 1975
- Ultrastructural analysis of the deeper layers of freeze-substituted guinea pig cortexBrain Research, 1974
- Rapid freezing and electron microscopy for the arrest of physiological processesJournal of Microscopy, 1974
- Extracellular space in frozen and ethanol substituted central nervous tissueThe Anatomical Record, 1970
- A STUDY OF EXTRACELLULAR SPACE IN CENTRAL NERVOUS TISSUE BY FREEZE-SUBSTITUTIONThe Journal of cell biology, 1965
- Electron microscopy after rapid freezing on a metal surface and substitution fixationThe Anatomical Record, 1964