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Fig. 3
Cx40.8 co-localizes with the GalT-GFP transgene found in the Golgi during regeneration.
(A–C) Co-localization in untreated regenerating fins. (D–F). Co-localization in regenerating fins treated with 0.1% DMSO carrier. (G–I) Fins injected with10 µg/ml BFA/0.1% BFA to disrupt the Golgi show dispersal of both Cx40.8 and GalT-GFP signals. In D-I, nuclei (blue) are stained with TO-PRO3 detected in the far red channel. Arrows point to areas of overlap in F (intact Golgi) and I (remnants of intact Golgi). Scale bars in C and F, 10 μm.
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