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cldn1xenopus pharyngeal arch 

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Experiment details for cldn1

Chang DJ et al. (2010) Assay

Xclaudin 1 is required for the proper gastrulation in Xenopus laevis.

Gene Clone Species Stages Anatomy
cldn1.S laevis NF stage 29 and 30 pharyngeal arch

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  Fig. 1. Temporal and spatial expression pattern of Xclaudin 1 during Xenopus development. (A) Temporal expression pattern of Xclaudin 1 was detected by RT-PCR. Ornithine decarboxylase (ODC) primers were used to normalize the amount of cDNA template. (B) RT-PCR of gastrula stage embryos (st.10.5). Xclaudin 1 mRNA is enriched in animal pole region and dorsal marginal zone in embryos. Chd (chordin) and BMP 4 were used as each gene control of explanted tissue and EF1α also used as a loading control. (C–J) In situ hybridization of spatial expression of Xclaudin 1 during early Xenopus development. Whole-mount in situ hybridization was carried out using a digoxigenin-labeled riboprobe. (C) Oocyte, animal view. (D) 2-cell stage, animal view and vegetal view. (E) 4-cell stage, animal view and vegetal view. (F) One hundred and twenty-eight cell stage, animal view and vegetal view. (G) Gastrular stage, animal view. (H) Neurula stage, animal view. (I) stage 29/30 lateral view. pd, pronephric duct; pn, pronephrus; ov, optic vesicle; df, dorsal fin; ev, eye vesicle; br, branchial arch.

Gene Clone Species Stages Anatomy
cldn1.S laevis NF stage 29 and 30 pharyngeal arch

  cldn1 (claudin 1) gene expression in Xenopus laevis embryo, assayed via in situ hybridization, NF stage 29 and 30, lateral view, anterior left, dorsal up.