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Image Search Results
Journal: Journal of neurophysiology
Article Title: Optogenetic surface stimulation of the rat cervical spinal cord.
doi: 10.1152/jn.00461.2017
Figure Lengend Snippet: Fig. 3. Transduced neuronal cell types. Spinal sections were processed for immunoreactivity to NeuN, VGLUT2, GAD65, and ChAT to identify the neuronal cell types associated with the neurons transduced by ChR2-mCherry or Chronos-GFP adeno- associated viruses (AAV). White arrows highlight some of the positively stained GAD65, VGLUT2, and ChAT puncta that colocalized with transduced neurons. A–D: a representative spinal section transduced by ChR2-mCherry AAV (A; red) and stained for NeuN (B; blue), and VGLUT2 (C; green). D: merged view, indicating that the ChR2-mCherry AAV trans- duced neurons that are associated with glutamatergic neu- rotransmission. E–H: a second representative spinal section transduced by ChR2-mCherry AAV (E; red) stained for NeuN (F), and GAD65 (G). H: merged view showing that the ChR2- mCherry AAV transduced neurons associated with GABAergic transmission. I–L: a representative spinal section transduced by Chronos-GFP AAV (I; green) and stained for NeuN (J; blue), and VGLUT2 (K; red). The merged view is depicted in L indicating that the Chronos-GFP AAV transduced neurons associated with glutamatergic neurotransmission. M–P: a sec- ond representative spinal section transduced by Chronos-GFP AAV (M) and stained for NeuN (N), and GAD65 (O). The merged view is shown in P, indicating that the Chronos-GFP AAV also transduced neurons associated with GABAergic transmission. Q–T: a representative spinal section transduced by Chronos-GFP AAV (Q; green), NeuN (R; blue), and ChAT (S; red). The merged view is shown in T indicating that the Chronos vector also labels a small percentage of neurons associated with cholinergic transmission. Scale bar 20 m.
Article Snippet: Sections were washed with PBS 3 10 min at room temperature followed by blocking with 5% normal donkey serum (Sigma-Aldrich) in PBS for 1 h. Primary antibodies were then added to sections at the following dilutions:
Techniques: Staining, Transmission Assay, Plasmid Preparation