FIGURE

Fig. S6

ID

ZDB-FIG-080325-122

Publication

Lachnit et al., 2008 - Alterations of the cytoskeleton in all three embryonic lineages contribute to the epiboly defect of Pou5f1/Oct4 deficient MZspg zebrafish embryos

Other Figures

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Fig. S6

Maternal contribution to the YCL phenotype. (A, B) Alexa488-Phalloidin staining. (C–E) Anti-β-Tubulin antibody immunohistochemistry with secondary antibody/HRP/DAB detection. (A–C) 75% epiboly, (D, E) 50% epiboly embryos. (A, D) WT; (B, C, E) Mspg^m793. (E) Microtubule track formation in Mspg^m793 embryos is slightly distorted, but microtubule free patches are not observed. Scale bars: 100 μm.

Expression Data

Antibody:	Ab1-tubb
Fish:	WT pou5f3^m793/+ (AB)
Anatomical Terms:	blastoderm yolk
Stage Range:	50%-epiboly to 75%-epiboly

Expression Detail

Antibody Labeling

Phenotype Data

Fish:	pou5f3^m793/+ (AB)
Observed In:	yolk syncytial layer cortical cytoskeleton yolk syncytial layer microtubule
Stage Range:	50%-epiboly to 75%-epiboly

Phenotype Detail

Acknowledgments

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Reprinted from Developmental Biology, 315(1), Lachnit, M., Kur, E., and Driever, W., Alterations of the cytoskeleton in all three embryonic lineages contribute to the epiboly defect of Pou5f1/Oct4 deficient MZspg zebrafish embryos, 1-17, Copyright (2008) with permission from Elsevier. Full text @ Dev. Biol.