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Fig. 1
Head region of 5 d old zebrafish (Danio rerio) embryos from the negative control (A), embryos exposed to 4 mg/L benzophenone-2 (BP-2; B), and embryos exposed to 7 mg/L BP-2 (C). The micrographs show analysed areas of the greyscale version of the TRITC channel under the fluorescence microscope. An increase in size and intensity of the fluorescence signal after exposure to BP-2 compared to the solvent control (DMSO) could be observed.
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