A new approach for high-pressure freezing of primary culture cells: the fine structure and stimulation-associated transformation of cultured rabbit gastric parietal cells

2002 ◽  
Vol 208 (3) ◽  
pp. 158-166 ◽  
Author(s):  
A. Sawaguchi ◽  
K. L. Mcdonald ◽  
S. Karvar ◽  
J. G. Forte
1965 ◽  
Vol 10 (1) ◽  
pp. 13-21 ◽  
Author(s):  
G. Victor Rohrer ◽  
J. Randolph Scott ◽  
Walter Joel ◽  
Stewart Wolf

2001 ◽  
Vol 203 (3) ◽  
pp. 285-294 ◽  
Author(s):  
D. Studer ◽  
W. Graber ◽  
A. Al-Amoudi ◽  
P. Eggli

2005 ◽  
Vol 13 (5) ◽  
pp. 16-19
Author(s):  
P.A. Sims ◽  
C.A. Lockwood ◽  
J.D. Hardin

Fluorescent fusion proteins are widely used to visualize the localization of proteins in worms, fish, flies and tissue culture cells. We have used two different methods that use high pressure freezing (HPF) combined with correlative light microscopy (LM) and TEM. The first method uses fluorescence from live organisms immobilized in agarose followed by HPF and standard freeze substitution in dry solvent with osmium. This pre-embedding method optimizes ultrastructural preservation. A second, post-embedding method preserves fluorescence and immunoreactivity from embedded and polymerized thin sections. Here we describe post-embedding fluorescent integrated TEM images (F-TEM).


Epilepsia ◽  
2012 ◽  
Vol 53 ◽  
pp. 4-8 ◽  
Author(s):  
Shanting Zhao ◽  
Daniel Studer ◽  
Werner Graber ◽  
Sigrun Nestel ◽  
Michael Frotscher

2004 ◽  
Vol 52 (1) ◽  
pp. 1-12 ◽  
Author(s):  
Philippe Rostaing ◽  
Robby M. Weimer ◽  
Erik M. Jorgensen ◽  
Antoine Triller ◽  
Jean-Louis Bessereau

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