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Fig. 4. Representative light micrographs of gill sections from killifish that
demonstrate the localization of COX2 protein. Gill sections were incubated
with antibody 160126 (A,C), antibody 160126 and antigen (B), or antibody
5 (D). Peroxidase substrates used to label antibodies were brown
(160126=COX2) and blue (Na+/K+-ATPase). No
immunolabeling was observed in negative control sections that were incubated
with antibody 160126 and excess antigen followed by multilink (anti-mouse,
rabbit and donkey) secondary antibodies (B); however, strong immunolabeling
occurred in a population of epithelial cells with antibody 160126 (A). In
serial sections, immunolabeling with antibody 160126 was always in cells with
Na+/K+-ATPase (C,D); arrows mark cells that stained with
both antibodies. Lamellae are numbered for clarity. Scale bars, 50 µm.