FIGURE

Fig. S1

ID

ZDB-FIG-151214-49

Publication

Roxo-Rosa et al., 2015 - The zebrafish Kupffer's vesicle as a model system for the molecular mechanisms by which the lack of Polycystin-2 leads to stimulation of CFTR

Other Figures

All Figure Page

Back to All Figure Page

Fig. S1

cup mutant KV volumes. Whole KV live-microscopy scans of 10–11 s.s. embryos from cup^+/- ; foxj1a:GFP parents. The middle focal plan along the XY axis and the respective orthogonal views (along XZ and YZ axes) are shown for the most representative normal tail (cup^+/-; cup^+/+) (A), and curly-up tail (cup^-/-) (B) embryos. KV^volume is indicated in µm³ and in picoL. Scale bars: 10 µm. (C) Estimated KV volumes (µm³) for normal tail (cup^+/-; cup^+/+) (n = 23) and curly-up tail (cup^-/-) (n = 15) embryos. Average values and the respective s.d. are indicated.

Expression Data

Genes:	GFP pkd2
Antibodies:	Ab1-tuba Ab2-pkd2
Fish:	pkd2^tc321/tc321 zf417Tg pkd2^tc321/tc321; zf417Tg
Anatomical Terms:	Kupffer's vesicle epithelial cell pronephric duct ciliary basal body pronephric duct motile cilium
Stage Range:	10-13 somites to Prim-25

Expression Detail

Antibody Labeling

Phenotype Data

Fish:	pkd2^tc321/tc321; zf417Tg
Observed In:	Kupffer's vesicle
Stage:	10-13 somites

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 @ Biol. Open