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Experiment details for ncam1

Satow R et al. (2002) Assay

Molecular cloning and characterization of dullard: a novel gene required for neural development.

Gene Clone Species Stages Anatomy
ncam1.L laevis NF stage 28 brain , spinal cord , central nervous system

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  Fig. 4. Microinjection of dullard Mo suppressed expression of neural markers. Control morpholino oligonucleotide (A, C, E, G, I, K) or dullard Mo (B, D, F, H, J, L) (40 ng) together with lacZ mRNA (200 pg) as a tracer was injected into a dorsal animal blastomere of8-cell embryos. Embryos were harvested at the early tail-bud stage (A–D) or the neurula stage (remaining panels) and analyzed by whole mount in situ hybridization with the indicated probes. In the dullard Mo-injected side ofthe embryo, expression ofthese markers is downregulated (B, D, F, H, J, L), while no change is observed in the control morpholino oligonucleotide-injected embryos (A, C, E, G, I, K). (A and B) lateral view, (C–F) dorsal view, (G–L) anterior view.