XB-IMG-77774
Xenbase Image ID: 77774
Fig. 7. Injection of SoxD MO into Xenopus embryos resulted in a neural defect phenotype. (A) Western blot analysis of HA-tagged proteins. SDS-PAGE was performed with protein prepared from embryos injected with 1 ng SoxD-HA(UTR+) or SoxD-HA(UTR−) mRNA either with or without 40 ng SoxD MO and cultured until stage 9. α-Actin served as an internal control. (B–D) Phenotype of embryos injected with 20 ng SoxD MO. (B) Uninjected embryo. (C) SoxD MO was injected into dorsal-animal blastomeres of eight-cell-stage embryos. (D) Linerized pCS2-SoxD-ORF (100 pg) was co-injected with SoxD MO into dorsal-animal blastomeres of eight-cell-stage embryos. (E–J) Whole-mount in situ hybridization analysis of terminal differentiation markers N-tubulin (E–H) and N-CAM (I,J). Embryos were injected with 40 ng SoxD MO into dorsal-animal blastomeres of eight-cell-stage embryos (F,H,J) and cultured until stage 15 (E,F) or 25 (G–J). (E,F) Dorsal view. Image published in: Nitta KR et al. (2004) Copyright © 2004. Image reproduced with permission of the Publisher, Elsevier B. V.
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