Literature DB >> 2038038

Cryofixation methods for ion localization in cells by electron probe microanalysis: a review.

K Zierold1.   

Abstract

Electron probe microanalysis data on the intracellular content and distribution of electrolyte ions depends critically on the functional state of the cells at the moment of cryofixation. Whereas tissue specimens often require special in-situ freezing techniques, isolated and cultured cells can be frozen within their environmental medium under physiologically controlled conditions. Thus, they represent a feasible system to study functional ion-related intracellular parameters such as the K/Na ratio. Specifically modified freezing devices allow the study of ion shifts related to dynamic processes in cells, for example, locomotion and exocytosis. The time resolution achieved by time-controlled cryofixation is approximately 1 ms.

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Year:  1991        PMID: 2038038     DOI: 10.1111/j.1365-2818.1991.tb03096.x

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  9 in total

1.  The frog neuromuscular junction revisited after quick-freezing-freeze-drying: ultrastructure, immunogold labelling and high resolution calcium mapping.

Authors:  R Pezzati; F Grohovaz
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1999-02-28       Impact factor: 6.237

2.  A combined solution exchange/plunge-freezing device for skinned muscle fibers.

Authors:  H Stegmann; R H Fink
Journal:  J Muscle Res Cell Motil       Date:  1999-08       Impact factor: 2.698

3.  High resolution ultrastructural mapping of total calcium: electron spectroscopic imaging/electron energy loss spectroscopy analysis of a physically/chemically processed nerve-muscle preparation.

Authors:  F Grohovaz; M Bossi; R Pezzati; J Meldolesi; F T Tarelli
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-14       Impact factor: 11.205

4.  Preparation of Cultured Cells Using High-Pressure Freezing and Freeze Substitution for Subsequent 2D or 3D Visualization in the Transmission Electron Microscope.

Authors:  Nicole Doyle; Philippa C Hawes
Journal:  Methods Mol Biol       Date:  2020

5.  Ultrastructural study of mast cells stimulated with compound 48/80 as revealed by quick-freezing method.

Authors:  I Takayama; Y Fujii; S Ohno; M A Fujino
Journal:  Virchows Arch       Date:  1994       Impact factor: 4.064

6.  Assessment of different sample preparation routes for mass spectrometric monitoring and imaging of lipids in bone cells via ToF-SIMS.

Authors:  Kaija Schaepe; Julia Kokesch-Himmelreich; Marcus Rohnke; Alena-Svenja Wagner; Thimo Schaaf; Sabine Wenisch; Jürgen Janek
Journal:  Biointerphases       Date:  2015-03-19       Impact factor: 2.456

7.  X-ray microanalysis of rat mast cells stimulated with compound 48/80 in combination with quick-freezing method.

Authors:  I Takayama; Y Fujii; S Ohno; M A Fujino
Journal:  Virchows Arch       Date:  1994       Impact factor: 4.064

8.  Preserving elemental content in adherent mammalian cells for analysis by synchrotron-based x-ray fluorescence microscopy.

Authors:  Qiaoling Jin; Tatjana Paunesku; Barry Lai; Sophie-Charlotte Gleber; S I Chen; Lydia Finney; David Vine; Stefan Vogt; Gayle Woloschak; Chris Jacobsen
Journal:  J Microsc       Date:  2016-08-31       Impact factor: 1.758

9.  Preparation of cultured cells using high-pressure freezing and freeze substitution for subsequent 2D or 3D visualization in the transmission electron microscope.

Authors:  Philippa C Hawes
Journal:  Methods Mol Biol       Date:  2015
  9 in total

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