Fig. S5
- ID
- ZDB-FIG-100504-36
- Publication
- Carney et al., 2010 - Genetic analysis of fin development in zebrafish identifies furin and hemicentin1 as potential novel Fraser Syndrome disease genes
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Fras1 distribution is compromised in sturgeon mutant fins. Transverse sections of WT (A) or stu-/- (B) posterior medial fins at 32 hpf, fluorescently immunostained for Fras1 (green), p63 (pink) and DAPI (blue). The extent of relative proximal extension of Fras1 protein appears reduced in stu-/- embryos (B) compared to WT (A). Extent of Fras1 staining is delineated by adjacent white line. Note that in the mutant, levels of Fras1 protein in the smaller domain appear correspondingly higher. |