vglut2, rabbit polyclonal antibody Search Results


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OriGene vglut2
Fig. 3. Transduced neuronal cell types. Spinal sections were processed for immunoreactivity to NeuN, <t>VGLUT2,</t> 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.
Vglut2, supplied by OriGene, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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GeneTex polyclonal rabbit vesicular glutamate transporter 2 (vglut2
Fig. 3. Transduced neuronal cell types. Spinal sections were processed for immunoreactivity to NeuN, <t>VGLUT2,</t> 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.
Polyclonal Rabbit Vesicular Glutamate Transporter 2 (Vglut2, supplied by GeneTex, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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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.

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: VGLUT2 (1:100; Origene Technologies, Rockville, MD; Zhang et al. 2018), GAD65 (1:500, Millipore, Billerica, MA; Besser et al. 2015), Synaptophysin (1:500, mouse host, Thermo Fisher Scientific, Waltham, MA; Haltas et al. 2012), Synaptophysin (1:250, rabbit host, Thermo Fisher Scientific; DeAndrade et al. 2012), NeuN (1:500, Millipore; for certificates of analysis see www.emdmillipore.com), ChAT (1:100; Millipore; Milan et al. 2015), and GFAP-Alexa Fluor 488 (1:500; Thermo Fisher Scientific; Xing et al. 2012).

Techniques: Staining, Transmission Assay, Plasmid Preparation