Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Search Criteria
Gene/CloneSpeciesStageAnatomy ItemExperimenter
cartptxenopus hypophysis 

Too many results?Too few results?

Experiment details for cartpt

Roubos EW et al. (2008) Assay



Gene Clone Species Stages Anatomy
cartpt.L laevis NF stage 66 hypophysis

  Fig. 3. CARTp-immunoreactive perikarya in the diencephalon and the mesencephalon. A: Immunoreactivity in the rostral diencephalon. Note stained cells in the nucleus of Bellonci (B; arrows). B: Immunoreactive cells and fibers in the infundibulum (inf) and the dorsal hypothalamic nucleus (dHy). C: Stained cells of the magnocellular preoptic nucleus (Mg) in the wall of the infundibulum (inf). Note that their long dendrites are oriented laterally, toward the surface of the brain. D: Immunoreactive cells in the hypothalamus and the Edinger- Westphal (EW) nucleus and intensely stained axon terminals in the neural lobe of the pituitary gland (pn). Sagittal section. Rostral is to the left. E: Immunostained infundibular neurons with long dendrites at the level of plane E in Figure 1. Note stained perikarya in the ventromedial (VM) and the posterior entopeduncular nuclei (epp). F: Immunostained fibers in the pars nervosa (pn) of the pituitary gland and median eminence of the hypothalamus. The intermediate pituitary lobe (pi) is immunonegative, whereas some cells in the distal lobe (pd) reveal weak immunoreactivity. G: Detail of the median eminence, with small and less numerous stained dots in the internal zone (iz) and large stained dots and short varicose fibers in the external zone (ez). Hd, dorsal habenula; Hv, ventral habenula. 3rd, third ventricle. Scale bar 200 m in A,B; 100 m in C,E; 300 m in D; 150 m in F; 15 m in G.

Gene Clone Species Stages Anatomy
cartpt.L laevis NF stage 66 hypophysis

  Fig. 6. Immunoelectron microscopy of CARTp immunoreactivity in the neural lobe of the pituitary gland of X. laevis. A: Conventional fixation. Low-power micrograph with neurohemal axon terminals (a) and a capillary (c) with endothelial cell (e) and blood cell (b). B: Conventional fixation. Round secretory granules (g) in neurohemal axon terminal, with some immunogold particles (arrowheads) indicating the presence of CARTp. C: High-pressure freezing and cryosubstitution followed by silver intensification of postembedding immunogold labeling, showing strongly immunopositive neurohemal terminals (a). D: As in C but the axon terminal is shown in detail. E: As in C but immunonegative, as sections were processed with antiserum preadsorbed to CARTp. s, intercellular space. Scale bar 1 m in A,C; 100 nm in B; 250 nm in D; 300 nm in E.