mouse anti-glun1 Search Results


mouse anti-glun1  (Becton Dickinson)
90
Becton Dickinson mouse anti-glun1
( a ) Cortical cells were fixed at 10 DIV and stained for NeuN (green) and GFAP (red) and with Hoechst (blue). The scale bar represents 100 µm. ( b ) The number of NeuN- and GFAP-positive cells was counted. Results were expressed as the percentage of these cells among the total number of Hoechst-positive cells and as the means ± SE in 4 independent experiments. ( c ) Proteins from cultured cortical neurons at 2, 4, 6, 8, 10 and 12 DIV were analyzed by immunoblotting with <t>anti-GluN1,</t> anti-GluN2A, anti-GluN2B, and anti-β-actin antibodies. Bands corresponding to GluN1, GluN2A, and GluN2B were scanned, the scanned bands were normalized by each protein at 2 DIV on the same blot. β-actin was used as a loading control. Results are the means ± SE (n = 4 independent experiments).
Mouse Anti Glun1, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+anti-glun1/pmc05980093-150-10-13?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
mouse anti-glun1 - by Bioz Stars, 2026-08
90/100 stars
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monoclonal mouse antiglun1  (Synaptic Systems)
90
Synaptic Systems monoclonal mouse antiglun1
( a ) Cortical cells were fixed at 10 DIV and stained for NeuN (green) and GFAP (red) and with Hoechst (blue). The scale bar represents 100 µm. ( b ) The number of NeuN- and GFAP-positive cells was counted. Results were expressed as the percentage of these cells among the total number of Hoechst-positive cells and as the means ± SE in 4 independent experiments. ( c ) Proteins from cultured cortical neurons at 2, 4, 6, 8, 10 and 12 DIV were analyzed by immunoblotting with <t>anti-GluN1,</t> anti-GluN2A, anti-GluN2B, and anti-β-actin antibodies. Bands corresponding to GluN1, GluN2A, and GluN2B were scanned, the scanned bands were normalized by each protein at 2 DIV on the same blot. β-actin was used as a loading control. Results are the means ± SE (n = 4 independent experiments).
Monoclonal Mouse Antiglun1, supplied by Synaptic Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+anti-glun1/pm34158618-253-40-45?v=Synaptic+Systems
Average 90 stars, based on 1 article reviews
monoclonal mouse antiglun1 - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

Image Search Results


( a ) Cortical cells were fixed at 10 DIV and stained for NeuN (green) and GFAP (red) and with Hoechst (blue). The scale bar represents 100 µm. ( b ) The number of NeuN- and GFAP-positive cells was counted. Results were expressed as the percentage of these cells among the total number of Hoechst-positive cells and as the means ± SE in 4 independent experiments. ( c ) Proteins from cultured cortical neurons at 2, 4, 6, 8, 10 and 12 DIV were analyzed by immunoblotting with anti-GluN1, anti-GluN2A, anti-GluN2B, and anti-β-actin antibodies. Bands corresponding to GluN1, GluN2A, and GluN2B were scanned, the scanned bands were normalized by each protein at 2 DIV on the same blot. β-actin was used as a loading control. Results are the means ± SE (n = 4 independent experiments).

Journal: Scientific Reports

Article Title: Furin inhibitor protects against neuronal cell death induced by activated NMDA receptors

doi: 10.1038/s41598-018-23567-0

Figure Lengend Snippet: ( a ) Cortical cells were fixed at 10 DIV and stained for NeuN (green) and GFAP (red) and with Hoechst (blue). The scale bar represents 100 µm. ( b ) The number of NeuN- and GFAP-positive cells was counted. Results were expressed as the percentage of these cells among the total number of Hoechst-positive cells and as the means ± SE in 4 independent experiments. ( c ) Proteins from cultured cortical neurons at 2, 4, 6, 8, 10 and 12 DIV were analyzed by immunoblotting with anti-GluN1, anti-GluN2A, anti-GluN2B, and anti-β-actin antibodies. Bands corresponding to GluN1, GluN2A, and GluN2B were scanned, the scanned bands were normalized by each protein at 2 DIV on the same blot. β-actin was used as a loading control. Results are the means ± SE (n = 4 independent experiments).

Article Snippet: The following primary antibodies were used: mouse anti-β-actin (a5441, Sigma), mouse anti-GluN1 (556308, BD Biosciences, Franklin Lakes, NJ, USA), rabbit anti-GluN2A (AB1555P, Millipore), mouse anti-GluN2B (610416, BD Biosciences), and rabbit anti-calpain-2 (39165, Abcam).

Techniques: Staining, Cell Culture, Western Blot