FIGURE

Fig. 2

ID

ZDB-FIG-080301-2

Publication

Sarmah et al., 2007 - A role for the inositol kinase Ipk1 in ciliary beating and length maintenance

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Fig. 2

ipk1 knockdown does not affect ciliary axoneme organization. (A and B) TEM cross-sections of cilia in KV for uninjected (A) and ipk1 ^MO1 (B) embryos. (C and D) Longitudinal TEM sections showing axonemal microtubules in KV cilia in uninjected (C) and ipk1 ^MO1 (D) embryos. (E–I) TEM sections showing pronephric duct cilia (E, F, and G) and spinal canal cilia (H and I). Enlarged images of independent pronephric duct cilia TEM sections are shown in G. Cilia sections in uninjected (E, G-I, G-III, G-V, and H) and ipk1 ^MO1 (F, G-II, G-IV, G-VI, and I) embryos are shown. In G–I, numerical tags are assigned to each of the nine outer microtubule doublets for reference to dynein arms in the text. (Scale bars, 0.1 μm.)

Expression Data

Expression Detail

Antibody Labeling

Phenotype Data

Fish:	WT + MO1-ippk
Knockdown Reagent:	MO1-ippk
Observed In:	central canal axoneme Kupffer's vesicle axoneme pronephric duct axoneme
Stage Range:	1-4 somites to Prim-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 @ Proc. Natl. Acad. Sci. USA