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High Pressure Freezing has Come of Age - but is it Mature?

Published online by Cambridge University Press:  02 July 2020

Kent McDonald*
Affiliation:
Electron Microscope Laboratory, 26 Giannini Hall, University of California, Berkeley, CA94720
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Extract

It should be no secret by now that ultrarapid freezing is a superior method of specimen preparation for many biological EM projects, and that high pressure freezing is the most versatile of the freezing methods. While cryopreservation is not necessary for all EM studies, it is the method of choice for high resolution work and where “fixation artifacts”, such as distorted membranes, or extraction of the cytosol is a problem. It is true that the machines are expensive, and not always immediately available, but for some questions it is the appropriate technology to use. In the U.S., there are machines available for general use in the far West (Berkeley, CA), the upper Midwest (Madision, WI and Minneapolis, MN), and in the Northeast (Albany, NY). For locations of any of the other 8 machines around the country, interested users can call Technotrade, International at (603) 622-5011.

Current Status of High Pressure Freezing: A decade ago, Studer et al. wrote an article entitled: “High Pressure Freezing Comes of Age” that illustrated how high pressure freezing (HPF) had become a proven technology, useful for preserving ultrastructure with unmatched fidelity in cell types that had previously been difficult to fix well for electron microscopy (EM).

Type
Cryotechniques, Immunocytochemistry, and Electron Microscopy II. Cells and Tissues
Copyright
Copyright © Microscopy Society of America

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References

1.Studer, D.et al.Scanning Microscopy Supplement 3 (1989) 253.Google Scholar
2.Kiss, J.Z. and Staehelin, L.A., in Rapid Freezing, Freeze Fracture and Deep Etching, Severs, N.J. and Shotton, D.M. (Eds), Wiley-Liss, Inc. (1995)89.Google Scholar
3.Bourett, T.M.et al., Fungal Genet. Biol . 24(1998)3.CrossRefGoogle Scholar
4.Hohenberg, H.et al., J. Microsc. 175(1994)34.CrossRefGoogle Scholar
5.Hohenberg, H.et al., J. Microsc. 183(1996)16.CrossRefGoogle Scholar
6.Shimoni, E. and Miiller, M.. J. Microsc. 192(1998)236.CrossRefGoogle Scholar
7.Thijssen, M.H.et al., J. Microsc. 192(1998)228.CrossRefGoogle Scholar