FIGURE

Fig. S6

ID

ZDB-FIG-110930-2

Publication

Wythe et al., 2011 - Hadp1, a newly identified pleckstrin homology domain protein, is required for cardiac contractility in zebrafish

Other Figures

All Figure Page

Back to All Figure Page

Fig. S6

Knockdown by a second, non-overlapping MO decreases levels of WT hadp1 mRNA and results in similar circulation defects as hadp1SBMO1. (A-B) Schematic representation of Hadp1 protein and partial genomic structure (boxes represent coding exons), with positions of the MO and RT-PCR primers indicated. (B) Agarose gel images show RT-PCR results for hadp1 message and β-actin as a loading control. -RT indicates RT without reverse transcriptase as a negative control. DNA ladder sizes are indicated in basepairs. (C-E) Brightfield images of live embryos anterior to left show overall trunk morphology in control (10 ng control MO) and hadp1 morphants (10 ng hadp1SBMO1, 5ng hadp1SBMO1, hadp1SBMO2). (F-H) Microangiography was performed following injection of hadp1SBMO1, hadp1SBMO2 or control MO. Circulation was scored by microangiography, or under transmitted light, and the results are quantified in (I). All embryos are imaged from a lateral view, anterior to left. The heart (H), common cardinal vein (CCV), dorsal aorta (DA), and posterior cardinal vein (PCV) are indicated.

Expression Data

Expression Detail

Antibody Labeling

Phenotype Data

Fish:	AB + MO2-plekha7a
Knockdown Reagent:	MO2-plekha7a
Observed In:	blood circulation pericardium
Stage:	Long-pec

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 @ Dis. Model. Mech.