IMAGE
Fig. 3
Image
|
Figure Caption
Fig. 3
Characterizing the phenotype caused by Efhc2 knock-down. a and b WISH for pronephros segment specific genes on 48 hpf morpholino injected embryos. Expression of slc20a1a (PCT), trpm7 (PST), slc12a1 (DE), slc12a3 (DL) and stc1 (CS) in efhc2 mismatch control (efhc2-MM) and splice-blocking morpholino (efhc2-Mo) injected embryos. The phenotype caused by Efhc2 knock-down was rescued by co-injecting efhc2 mRNA along with efhc2 morpholino. c Schematic representation of defects caused by Efhc2 knock-down
Figure Data
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 Biosci.