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
prphxenopus   

Too many results?Too few results?

Experiment details for prph

Martinez-De Luna RI et al. (2017) Assay

Müller glia reactivity follows retinal injury despite the absence of the glial fibrillary acidic protein gene in Xenopus.

Gene Clone Species Stages Anatomy
prph.L laevis NF stage 50 retina , brain , spinal cord , ventricular zone , ciliary marginal zone , [+]

Display additional annotations [+]
  Fig. 5. Expression patterns of vim, des, prph, ina, and nes in the pre-metamorphic tadpole nervous system. In situ hybridization on retinal, brain and spinal cord sections for vim (A–C), des (D–F), prph (G-I), ina (J–L), and nes (M–O). Sections were obtained from pre-metamorphic stage 50 tadpoles. Location of the lens (L), outer (O), inner (I) and ganglion (G) cell layers are indicated. Scale bars, 100 µm in A, D, G, J and M; all others are 50 µm.

Gene Clone Species Stages Anatomy
prph.L laevis NF stage 51 to NF stage 52 retinal ganglion cell layer

Display additional annotations [+]
  Fig. 7. Retinal expression of intermediate filament proteins after retinal ganglion cell axotomy. vim (A and B), prph (E and F), and ina (I and J) in situ hybridization on retinal sections from control unoperated (A, E, and I) and operated (retinal axotomy) (B, F, and J) eyes. Vim mAb (C and D), Prph pAb 1 (G and H), and R5 mAb (K and L) immunolabeling of retinal sections from control (C, G, and K) and operated (D, H, and L) eyes. Rod photoreceptors were labeled with either GαT1 (Transducin) pAb (C and D) or XAP-2 mAb (G, H, K, and L). Sections were counterstained with DAPI to visualize nuclei. Scale bars, 50 µm.