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Whole-mount immunolocalization of zebrafish CYP1A protein in a representative DMSO vehicle (control) larva (A,B) and 30 µM retene-exposed (C,D) larvae at 48 hpf using mAb CRC2. Each larva was exposed to their respective treatment from 4 hpf through 48 hpf. BA, brachial vasculature; BV, brain vasculature; H, heart; UP, urogenital pore; PVP, posterior vascular plexus; ISV, intersegmental vessel. Details are found in Methods.
