FIGURE

Fig. 8.

ID
ZDB-FIG-110712-27
Publication
Bruses, 2011 - N-cadherin regulates primary motor axon growth and branching during zebrafish embryonic development
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Fig. 8.

Tg(mnx1:Gal4-VP16) embryos were injected at the one-cell stage with a plasmid encoding pren-EGFP under a 14X-UAS element, fixed at 24 hpf, and immunostained with SV2 and znp1 antibodies. Arrowheads point to primary motor neurons expressing EGFP. B,D: Higher magnification images of the boxed areas in A,C, respectively. Arrowheads point to primary motor neuron somas. E–I: Tg(mnx1:Gal4-VP16) embryos were injected at the one-cell stage with the 14X-UAS-IL2α-EGFP plasmid (E,F) or with 14X-UAS-IL2α-CD and pren-EGFP plasmid (G–I). Embryos were fixed at 24 hpf and immunostained with anti-IL2α antibodies (F,H,I). IL2α-EGFP is evenly distributed throughout the motor neuron (E,F). Pren-EGFP labels the entire cell body and axon (G), whereas IL2α-CD is detected as discrete puncta through out the cell (H, arrowheads). I: Higher magnification of the axon shown in G, indicating IL2α-CD puncta accumulated at the choice point (bracket) and at the distal tip of the axon. Dorsal is to the top and rostral is to the left. Scale bars = 50 μm in C (applies to A,C); 10 µm in D (applies to B,D); 10 μm in F (applies to E,F); 10 μm in H (applies to G,H).

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data

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 @ J. Comp. Neurol.