By John H. Luft (auth.), James K. Koehler Ph. D. (eds.)
The previous decade has visible a notable bring up within the use of electron microscopy as a researm software in biology and drugs. hence, such a lot institu tions of upper studying now boast a number of electron optical laboratories having a variety of degrees of class. education within the regimen use of elec tron optical apparatus and interpretation of effects isn't any longer limited to a couple prestigious facilities. nonetheless, temniques used by researm staff within the ultrastructural area became super assorted and intricate. even though a great number of really very good volumes of electron microscopic temnique are actually devoted to the fundamental components on hand whim enable the beginner to procure a cheap creation to the sector, really few books were dedicated to a dialogue of extra advert vanced temnical points of the artwork. It was once with this view that the current quantity was once conceived as a convenient reference for employees already having a few history within the box, as a knowledge resource for these wishing to shift efforts into extra promising temniques, or to be used as a complicated path or seminar consultant. material has been mosen fairly at the foundation of pertinence to provide researm actions in organic electron microscopy and emphasis has been given these parts whim appear destined to significantly extend in precious ness within the close to future.
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Extra resources for Advanced Techniques in Biological Electron Microscopy
In retrospect, the low viscosity of the methacrylates made them a delight to use. The high viscosity of the unpolymerized (liquid) polyester and epoxy resins, in addition to ethetic faults, caused technical difficulties. The most serious was the failure to achieve complete mixing of the components of the resin, and particularly, of the small amounts of accelerator. The tech- niques appropriate for aqueous chemistry, such as shaking to mix, rely on generating turbulence, and turbulent mixing is useless in highly viscous fluids.
Cytol. 4, 191-194 (1958). GLAUERT, A. , ROGERS, G. , GLAUERT, R. : A new embedding medium for electron microscopy. ) 178, 803 (1956). HAYAT, M. : Principles and Techniques of Electron Microscopy: Biological Applications, Vol. 1. New York: Van Nostrand, Reinhold Co. 1970. HENDRY, J. , HOMER, R. , ROSE, F. , WALPOLE, A. : Cytotoxic agents: II, bisepoxides and related compounds. Brit. J. Pharmacol. 6, 235-255 (1951). JOY, R. , FINEAN, J. : A comparison of the effects of freezing and of treatment with hypertonic solutions on the structure of nerve myelin.
Anat. Rec. 148, 343-344 (1964a). : Electron microscopy of the interaction of ruthenium violet with the cell membrane complex of Amoeba proteus. J. Cell BioI. 23, 92A (1964b). : "New membrane" formation in Amoeba proteus upon injury of individual cells. J. Cell BioI. 49, 747-772 (1971). , LUFT, J. : Ruthenium red and violet. III. Fine structure of the plasma membrane and extraneous coats in Amoebae (A. proteus and Chaos chaos). Anat. Rec. 171,417-441 (1971). , LUFT, J. : Osmotic damage to cells from viscous embedding media.