By M. T. Silva (auth.), Robert M. Burton, Francisco Carvalho Guerra (eds.)

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An. Soc. Port. M. E. ,abs. 30 (1982). 28. D. C. Pease, Phosphotungstic acid as an electron stain,26th Ann. Meet. E. M. Soc. ,pg. 36 (1968). 29. A. Rambourg ,Morphological and histochemical aspects of gylcoproteins of the surface of animal cells, Int. J. , 31 :57 (1971). 30. J. C. Roland, C. A. Lemhi and D. J. ,47:195 (1972) • 31. J. -E. FlOChon and D. Huneau, Validity of phos};tlotungstic acid staining of polysaccharides (glycogen) at very low pH on thin sections of glycolmethacrylate embedded material, J.

Port. M. ,abs 13M (1980). 88. M. S. Wachter and R. C. Johnson , Treponema outer envelope: chemical analysis,Proc. Soc. Exptl. Bio. , 151 :97 (1976). 89. L. -S. Kim,Mycobacterium,Bacteriol. , 41 :217 (1977). 90. M. R. J. -H. Lim,Quantitative inmunoelectrophoresis technique in studies of identification,purification and distribution of membrane lipcmannan,in "Chemistry and biological activities of bacterial surface amphiphiles" ,G. D. Shockman and A.. J. Wicken,eds. ,Acad. Press,New York,pg. 101 (1981).

30:192 (1966). F. Op den Kamp Department of Biochemistry University of Utrecht Padualaan 8 Utrecht, The Netherlands INTRODUCTION It is only about one decade ago when it was for the first time proposed that the phospholipids in a biological membrane might be distributed over both halves of the bilayer in a highly asymmetric fashion. This proposal of Bretscher was based on the observations that treatment of intact erythrocytes with NH2-grouP specific reagents does not result in the labeling of appreciable quantities of the amino-phospholipids, phosphatidylethanolamine (PE) and phosphatidylserine (PS), whereas these phospholipids could be easily labeled when open ghost membranes were exposed to the reagents (1).

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