FIGURE

Fig. S3

ID
ZDB-FIG-151009-31
Publication
Jia et al., 2015 - Mutation of kri1l causes definitive hematopoiesis failure via PERK-dependent excessive autophagy induction
Other Figures
All Figure Page
Back to All Figure Page
Fig. S3

WISH analysis of primitive hematopoiesis and vascular morphogenesis. WT or mutantcas002 embryos were fixed at 22 hpf, followed by WISH analysis of scl, gata1, spi1, mpo expression. Expression of scl (A-B), gata1 (C-D), spi1 (E-F) and mpo (G-H) show no significant difference between wild-type siblings and mutants at 22 hpf. Insets in E-F show dorsal views of the head staining region. Embryos were fixed at 26 dpf, followed by WISH analysis of expression pattern of kdr. Expression of kdr (I-J), which marks vascular endothelial, had no significant difference between siblings and mutants at 26 hpf. The number and percentage of het-het incross embryos with the in situ pattern are listed at the bottom of the Mutantcas002 panels.

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data
Fish:
Observed In:
Stage: 26+ 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 @ Cell Res.