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A new method of processing cultured cells for transmission electron microscopy: The floating sheet

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Journal of tissue culture methods

Summary

In this improved method of embedding tissue culture specimens,n-butylglycidyl ether is added to fixed, dehydrated cells within the plastic culture flasks. Then-butylglycidyl ether dissolves the flask, allowing a sheet of cells and a microscopic remnant of the plastic culture flask to separate from the culture dish and float freely on the surface of the ether. The layer of cells can then be folded or centrifuged; and upon examination the flask remnant can be located microscopically to determine orientation. This new method provides excellent morphology, greatly increased sample size, and marked reduction in processing time.

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References

  1. Allen, T. D. The application of scanning electron microscopy to cells in culture: selected methodologies. In: Bell, P.B., ed. Scanning electron microscopy of cells in culture. O'Hare, IL: Scanning Electron Miscroscopy, Inc.; 1984:19–28.

    Google Scholar 

  2. Aziz, P.; Davis, M. E. Thin-layer embedding of cell suspension for electron microscopy; a sandwich-in-cellophane technique. Stain Tech. 43(4):237–238; 1968.

    Google Scholar 

  3. Casey, M. L.; MacDonald, P. C.; Mitchell, M. D., et al. Maintenance and characterization of human myometrial smooth muscle cells in monolayer culture. In Vitro 20:396–403; 1984.

    PubMed  Google Scholar 

  4. Cavallo, T.; Graves, K.; Cole, N. L., et al. Cytomegalovirus: an ultrastructural study of the morphogenesis of nuclear inclusions in human cell culture. J. Gen. Virol. 56:97–104; 1981.

    PubMed  Google Scholar 

  5. Chang, J. P. A new technique for separation of coverglass substrate from epoxy-embedded specimens for electron microscopy. J. Ultrastruct. Res. 37:370–377; 1971.

    PubMed  Google Scholar 

  6. Dalen, H.; Nevalainen, T. J. Direct epoxy embedding for vertical sectioning of cells grown as a monolayer on millipore filter. Stain Tech. 43(4):217–220; 1969.

    Google Scholar 

  7. Hayat, M. A. In: Hayat, M. A., ed., Principles and techniques of electron microscopy, vol. 4. New York:Van Nostrand Reinhold, Co.; 1974:52–57.

    Google Scholar 

  8. Nelson, M. K.; Flaxman, B. A.In situ embedding and vertical sectioning for electron microscopy of tissue cultures grown on plastic petri dishes. Stain Tech. 47(5):261–284; 1972.

    Google Scholar 

  9. Reymond, O. L.; Pickett-Heaps, J. D. A routine flat embedding method for electron microscopy of microorganisms allowing selection and precisely orientated sectioning of single cells by light microscopy. J. Microsc. 130(1):79–84; 1983.

    PubMed  Google Scholar 

  10. Richters, A.; Valentin, P. L. Transmission electron microscopy of tissue culture preparations on polystyrene coverslips. Stain Tech. 48(4):185–188; 1973.

    Google Scholar 

  11. Wetzel, B.; Kendig, E. M.; Jones, G. M., et al. A systematic scanning electron microscopy (SEM) analysis of mitotic cell populations in monolayer culture. In: Bell, P. J., ed. Scanning electron microscopy of cells in culture. O'Hare, IL:Scanning Electron Miscroscopy, Inc., 1984:173–182.

    Google Scholar 

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Arnold, J.R., Boor, P.J. A new method of processing cultured cells for transmission electron microscopy: The floating sheet. Journal of Tissue Culture Methods 10, 223–226 (1986). https://doi.org/10.1007/BF01404481

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  • DOI: https://doi.org/10.1007/BF01404481

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