Fig. 3.
Fig. 3. Comparisons of the intracellular distribution of multimerin, von Willebrand factor, P-selectin, and CD63. Paired, epifluorescent microscopic images of structures in the cytoplasm of double-immunolabeled, quiescent, permeabilized endothelial cells are shown. Primary antibodies included monoclonal (a, vWf; b and c, multimerin; d, CD63) and polyclonal antisera (a and c, P-selectin; b, vWf; d, multimerin). Single-labeled coverslips, processed in parallel, showed the same pattern of labeling. Identical granules were labeled by antibodies to P-selectin and von Willebrand factor, but multimerin was found in a different distribution than von Willebrand factor, P-selectin, and CD63 (N indicates cell nuclei). Cells labeled with polyclonal antimultimerin (d) showed more background labeling of nongranular structures than the cells labeled with monoclonal antimultimerin (b and c).

Comparisons of the intracellular distribution of multimerin, von Willebrand factor, P-selectin, and CD63. Paired, epifluorescent microscopic images of structures in the cytoplasm of double-immunolabeled, quiescent, permeabilized endothelial cells are shown. Primary antibodies included monoclonal (a, vWf; b and c, multimerin; d, CD63) and polyclonal antisera (a and c, P-selectin; b, vWf; d, multimerin). Single-labeled coverslips, processed in parallel, showed the same pattern of labeling. Identical granules were labeled by antibodies to P-selectin and von Willebrand factor, but multimerin was found in a different distribution than von Willebrand factor, P-selectin, and CD63 (N indicates cell nuclei). Cells labeled with polyclonal antimultimerin (d) showed more background labeling of nongranular structures than the cells labeled with monoclonal antimultimerin (b and c).

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