FIGURE

Fig. 1

ID

ZDB-FIG-091217-73

Publication

Duldulao et al., 2009 - Cilia localization is essential for in vivo functions of the Joubert syndrome protein Arl13b/Scorpion

Other Figures

All Figure Page

Back to All Figure Page

Fig. 1

Phenotypes of sco^hi459 mutant zebrafish. (A) Side view of embryos at 36 hpf. (B) A mutant at 3 dpf. The arrow points to a cyst. (C,D) Cysts at the glomerular (arrowhead) and tubular (arrow) regions in cross-sections of mutant embryos at 50 hpf. (E-I) Increased size of the pronephric duct in mutant embryos as shown in cross-sections of the duct region (E,F red arrows) at 50 hpf. (G,H) The pronephric duct in side view in whole-mount embryos stained with α6F. (I) Cross sections of pronephric duct at 5 dpf. Anti-Na⁺/K⁺-ATPase and anti-Cdh17 are used as basolateral markers. Atypical PKC (aPKC) and rhodamine phalloidin (RhPh) are used as apical markers. DAPI is used as nuclei dye. mut, mutant; nc, notochord; wt, wild type. Scale bars: 10 μm.

Expression Data

Gene:	cdh17
Antibodies:	Ab1-atp1a1 Ab1-cdh17
Fish:	WT arl13b^{hi459Tg/hi459Tg}
Anatomical Term:	pronephric duct
Stage Range:	Long-pec to Day 5

Expression Detail

Antibody Labeling

Phenotype Data

Fish:	arl13b^{hi459Tg/hi459Tg}
Observed In:	post-vent region pronephric duct pronephric glomerulus pronephric tubule pronephros trunk
Stage Range:	Prim-25 to Day 5

Phenotype Detail

Acknowledgments

This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Development