glass bottom dishes Search Results


glass bottom petri 8 dish  (CELLTREAT Scientific)
94
CELLTREAT Scientific glass bottom petri 8 dish
Glass Bottom Petri 8 Dish, supplied by CELLTREAT Scientific, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/glass+bottom+dishes/Glass+Bottom+Dishes/pm41609467-105-12-20
Average 94 stars, based on 1 article reviews
glass bottom petri 8 dish - by Bioz Stars, 2026-10
94/100 stars
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glass bottom  (Cellvis Inc)
86
Cellvis Inc glass bottom
Glass Bottom, supplied by Cellvis Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/glass+bottom+dishes/bottom+dishes+glass/pmc12770385-312-9-12
Average 86 stars, based on 1 article reviews
glass bottom - by Bioz Stars, 2026-10
86/100 stars
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glass bottom cell culture dishes nest  (Boster Bio)
90
Boster Bio glass bottom cell culture dishes nest
Glass Bottom Cell Culture Dishes Nest, supplied by Boster Bio, 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/glass+bottom+dishes/Glass+Bottom+Cell+Cutlure+Dishes%2F+Plates/pmc07299723-117-15-47
Average 90 stars, based on 1 article reviews
glass bottom cell culture dishes nest - by Bioz Stars, 2026-10
90/100 stars
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mattek glass bottom dish  (Becton Dickinson)
90
Becton Dickinson mattek glass bottom dish
Mattek Glass Bottom Dish, 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/glass+bottom+dishes/mattek+glass+bottom+dish/pmc03002178-82-19-22
Average 90 stars, based on 1 article reviews
mattek glass bottom dish - by Bioz Stars, 2026-10
90/100 stars
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polystyrene dishes with inner circular glass bottoms  (MatTek)
90
MatTek polystyrene dishes with inner circular glass bottoms
Polystyrene Dishes With Inner Circular Glass Bottoms, supplied by MatTek, 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/glass+bottom+dishes/polystyrene+dishes+with+inner+circular+glass+bottoms/pmc11937866-244-2-11
Average 90 stars, based on 1 article reviews
polystyrene dishes with inner circular glass bottoms - by Bioz Stars, 2026-10
90/100 stars
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collagen-coated 35 mm glass bottom dishes with grids  (MatTek)
90
MatTek collagen-coated 35 mm glass bottom dishes with grids
Collagen Coated 35 Mm Glass Bottom Dishes With Grids, supplied by MatTek, 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/glass+bottom+dishes/collagen+coated+35+mm+glass+bottom+dishes+with+grids/pmc11446916-73-12-13
Average 90 stars, based on 1 article reviews
collagen-coated 35 mm glass bottom dishes with grids - by Bioz Stars, 2026-10
90/100 stars
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glass-bottom dishes suitable for fluorescent imaging  (MatTek)
90
MatTek glass-bottom dishes suitable for fluorescent imaging
Glycolysis and mitochondrial oxidative phosphorylation are necessary for VVEC proliferative and migratory responses. A : proliferation rates were determined in VVEC grown in DMEM/1% FBS in the presence of oligomycin (Oligo; 10 ng/ml), rotenone (Rot; 0.1 μM), 2-deoxyglucose (2-DG; 0.2 mM), and FCCP (0.5 μM) The media with indicated inhibitors were refreshed each second day. Cell proliferation rate was assessed using a <t>fluorescent</t> CyQuant proliferation kit. Values are means ± SE from 3 independent experiments. B : [ 3 H]thymidine incorporation was determined in growth-arrested VVEC (DMEM without serum, 72 h) in response to stimulation with extracellular ATP (100 μM). Cells remained untreated or were treated with 2-DG (2 mM), Rot (0.1 μM), Oligo (100 ng/ml), or FCCP (2 μM) 20 min before stimulation. Values are means ± SE from 3 independent experiments. ## P < 0.01. ### P < 0.001. * P < 0.05, ** P < 0.01, and *** P < 0.001 compared with ATP-treated cells. C : for migration assay, growth-arrested cells were seeded in Boyden chamber-permeable inserts and pretreated with the indicated for 20 min. ATP, MeSADP, or adenosine (Ado; 500 μM) were added to the lower compartment to initiate migration. Number of migrated cells was evaluated as described in methods . Values are means ± SE from 4 independent experiments. ### P < 0.001, control vs. ATP-stimulated cells. * P < 0.05, ** P < 0.01, and *** P < 0.01, untreated vs. treated with inhibitors.
Glass Bottom Dishes Suitable For Fluorescent Imaging, supplied by MatTek, 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/glass+bottom+dishes/glass+bottom+dishes+suitable+for+fluorescent+imaging/pmc05283894-78-8-10
Average 90 stars, based on 1 article reviews
glass-bottom dishes suitable for fluorescent imaging - by Bioz Stars, 2026-10
90/100 stars
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no.1 glass bottom culture dishes  (MatTek)
90
MatTek no.1 glass bottom culture dishes
Glycolysis and mitochondrial oxidative phosphorylation are necessary for VVEC proliferative and migratory responses. A : proliferation rates were determined in VVEC grown in DMEM/1% FBS in the presence of oligomycin (Oligo; 10 ng/ml), rotenone (Rot; 0.1 μM), 2-deoxyglucose (2-DG; 0.2 mM), and FCCP (0.5 μM) The media with indicated inhibitors were refreshed each second day. Cell proliferation rate was assessed using a <t>fluorescent</t> CyQuant proliferation kit. Values are means ± SE from 3 independent experiments. B : [ 3 H]thymidine incorporation was determined in growth-arrested VVEC (DMEM without serum, 72 h) in response to stimulation with extracellular ATP (100 μM). Cells remained untreated or were treated with 2-DG (2 mM), Rot (0.1 μM), Oligo (100 ng/ml), or FCCP (2 μM) 20 min before stimulation. Values are means ± SE from 3 independent experiments. ## P < 0.01. ### P < 0.001. * P < 0.05, ** P < 0.01, and *** P < 0.001 compared with ATP-treated cells. C : for migration assay, growth-arrested cells were seeded in Boyden chamber-permeable inserts and pretreated with the indicated for 20 min. ATP, MeSADP, or adenosine (Ado; 500 μM) were added to the lower compartment to initiate migration. Number of migrated cells was evaluated as described in methods . Values are means ± SE from 4 independent experiments. ### P < 0.001, control vs. ATP-stimulated cells. * P < 0.05, ** P < 0.01, and *** P < 0.01, untreated vs. treated with inhibitors.
No.1 Glass Bottom Culture Dishes, supplied by MatTek, 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/glass+bottom+dishes/no+1+glass+bottom+culture+dishes/pmc03642183-67-14-18
Average 90 stars, based on 1 article reviews
no.1 glass bottom culture dishes - by Bioz Stars, 2026-10
90/100 stars
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tirf glass-bottomed mattek dishes  (MatTek)
90
MatTek tirf glass-bottomed mattek dishes
Glycolysis and mitochondrial oxidative phosphorylation are necessary for VVEC proliferative and migratory responses. A : proliferation rates were determined in VVEC grown in DMEM/1% FBS in the presence of oligomycin (Oligo; 10 ng/ml), rotenone (Rot; 0.1 μM), 2-deoxyglucose (2-DG; 0.2 mM), and FCCP (0.5 μM) The media with indicated inhibitors were refreshed each second day. Cell proliferation rate was assessed using a <t>fluorescent</t> CyQuant proliferation kit. Values are means ± SE from 3 independent experiments. B : [ 3 H]thymidine incorporation was determined in growth-arrested VVEC (DMEM without serum, 72 h) in response to stimulation with extracellular ATP (100 μM). Cells remained untreated or were treated with 2-DG (2 mM), Rot (0.1 μM), Oligo (100 ng/ml), or FCCP (2 μM) 20 min before stimulation. Values are means ± SE from 3 independent experiments. ## P < 0.01. ### P < 0.001. * P < 0.05, ** P < 0.01, and *** P < 0.001 compared with ATP-treated cells. C : for migration assay, growth-arrested cells were seeded in Boyden chamber-permeable inserts and pretreated with the indicated for 20 min. ATP, MeSADP, or adenosine (Ado; 500 μM) were added to the lower compartment to initiate migration. Number of migrated cells was evaluated as described in methods . Values are means ± SE from 4 independent experiments. ### P < 0.001, control vs. ATP-stimulated cells. * P < 0.05, ** P < 0.01, and *** P < 0.01, untreated vs. treated with inhibitors.
Tirf Glass Bottomed Mattek Dishes, supplied by MatTek, 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/glass+bottom+dishes/tirf+glass+bottomed+mattek+dishes/pmc03663508-72-0-2
Average 90 stars, based on 1 article reviews
tirf glass-bottomed mattek dishes - by Bioz Stars, 2026-10
90/100 stars
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glass-bottom culture dishes  (Ibidi USA)
90
Ibidi USA glass-bottom culture dishes
Glycolysis and mitochondrial oxidative phosphorylation are necessary for VVEC proliferative and migratory responses. A : proliferation rates were determined in VVEC grown in DMEM/1% FBS in the presence of oligomycin (Oligo; 10 ng/ml), rotenone (Rot; 0.1 μM), 2-deoxyglucose (2-DG; 0.2 mM), and FCCP (0.5 μM) The media with indicated inhibitors were refreshed each second day. Cell proliferation rate was assessed using a <t>fluorescent</t> CyQuant proliferation kit. Values are means ± SE from 3 independent experiments. B : [ 3 H]thymidine incorporation was determined in growth-arrested VVEC (DMEM without serum, 72 h) in response to stimulation with extracellular ATP (100 μM). Cells remained untreated or were treated with 2-DG (2 mM), Rot (0.1 μM), Oligo (100 ng/ml), or FCCP (2 μM) 20 min before stimulation. Values are means ± SE from 3 independent experiments. ## P < 0.01. ### P < 0.001. * P < 0.05, ** P < 0.01, and *** P < 0.001 compared with ATP-treated cells. C : for migration assay, growth-arrested cells were seeded in Boyden chamber-permeable inserts and pretreated with the indicated for 20 min. ATP, MeSADP, or adenosine (Ado; 500 μM) were added to the lower compartment to initiate migration. Number of migrated cells was evaluated as described in methods . Values are means ± SE from 4 independent experiments. ### P < 0.001, control vs. ATP-stimulated cells. * P < 0.05, ** P < 0.01, and *** P < 0.01, untreated vs. treated with inhibitors.
Glass Bottom Culture Dishes, supplied by Ibidi USA, 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/glass+bottom+dishes/glass+bottom+culture+dishes/pm32492073-80-6-9
Average 90 stars, based on 1 article reviews
glass-bottom culture dishes - by Bioz Stars, 2026-10
90/100 stars
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glass-bottomed culture dishes  (MatTek)
90
MatTek glass-bottomed culture dishes
Glycolysis and mitochondrial oxidative phosphorylation are necessary for VVEC proliferative and migratory responses. A : proliferation rates were determined in VVEC grown in DMEM/1% FBS in the presence of oligomycin (Oligo; 10 ng/ml), rotenone (Rot; 0.1 μM), 2-deoxyglucose (2-DG; 0.2 mM), and FCCP (0.5 μM) The media with indicated inhibitors were refreshed each second day. Cell proliferation rate was assessed using a <t>fluorescent</t> CyQuant proliferation kit. Values are means ± SE from 3 independent experiments. B : [ 3 H]thymidine incorporation was determined in growth-arrested VVEC (DMEM without serum, 72 h) in response to stimulation with extracellular ATP (100 μM). Cells remained untreated or were treated with 2-DG (2 mM), Rot (0.1 μM), Oligo (100 ng/ml), or FCCP (2 μM) 20 min before stimulation. Values are means ± SE from 3 independent experiments. ## P < 0.01. ### P < 0.001. * P < 0.05, ** P < 0.01, and *** P < 0.001 compared with ATP-treated cells. C : for migration assay, growth-arrested cells were seeded in Boyden chamber-permeable inserts and pretreated with the indicated for 20 min. ATP, MeSADP, or adenosine (Ado; 500 μM) were added to the lower compartment to initiate migration. Number of migrated cells was evaluated as described in methods . Values are means ± SE from 4 independent experiments. ### P < 0.001, control vs. ATP-stimulated cells. * P < 0.05, ** P < 0.01, and *** P < 0.01, untreated vs. treated with inhibitors.
Glass Bottomed Culture Dishes, supplied by MatTek, 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/glass+bottom+dishes/glass+bottomed+culture+dishes/pmc03717236-36-35-38
Average 90 stars, based on 1 article reviews
glass-bottomed culture dishes - by Bioz Stars, 2026-10
90/100 stars
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gelatin-coated glass-bottom plate dishes  (MatTek)
90
MatTek gelatin-coated glass-bottom plate dishes
Glycolysis and mitochondrial oxidative phosphorylation are necessary for VVEC proliferative and migratory responses. A : proliferation rates were determined in VVEC grown in DMEM/1% FBS in the presence of oligomycin (Oligo; 10 ng/ml), rotenone (Rot; 0.1 μM), 2-deoxyglucose (2-DG; 0.2 mM), and FCCP (0.5 μM) The media with indicated inhibitors were refreshed each second day. Cell proliferation rate was assessed using a <t>fluorescent</t> CyQuant proliferation kit. Values are means ± SE from 3 independent experiments. B : [ 3 H]thymidine incorporation was determined in growth-arrested VVEC (DMEM without serum, 72 h) in response to stimulation with extracellular ATP (100 μM). Cells remained untreated or were treated with 2-DG (2 mM), Rot (0.1 μM), Oligo (100 ng/ml), or FCCP (2 μM) 20 min before stimulation. Values are means ± SE from 3 independent experiments. ## P < 0.01. ### P < 0.001. * P < 0.05, ** P < 0.01, and *** P < 0.001 compared with ATP-treated cells. C : for migration assay, growth-arrested cells were seeded in Boyden chamber-permeable inserts and pretreated with the indicated for 20 min. ATP, MeSADP, or adenosine (Ado; 500 μM) were added to the lower compartment to initiate migration. Number of migrated cells was evaluated as described in methods . Values are means ± SE from 4 independent experiments. ### P < 0.001, control vs. ATP-stimulated cells. * P < 0.05, ** P < 0.01, and *** P < 0.01, untreated vs. treated with inhibitors.
Gelatin Coated Glass Bottom Plate Dishes, supplied by MatTek, 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/glass+bottom+dishes/gelatin+coated+glass+bottom+dishes/pm27289182-98-12-16
Average 90 stars, based on 1 article reviews
gelatin-coated glass-bottom plate dishes - by Bioz Stars, 2026-10
90/100 stars
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Image Search Results


Glycolysis and mitochondrial oxidative phosphorylation are necessary for VVEC proliferative and migratory responses. A : proliferation rates were determined in VVEC grown in DMEM/1% FBS in the presence of oligomycin (Oligo; 10 ng/ml), rotenone (Rot; 0.1 μM), 2-deoxyglucose (2-DG; 0.2 mM), and FCCP (0.5 μM) The media with indicated inhibitors were refreshed each second day. Cell proliferation rate was assessed using a fluorescent CyQuant proliferation kit. Values are means ± SE from 3 independent experiments. B : [ 3 H]thymidine incorporation was determined in growth-arrested VVEC (DMEM without serum, 72 h) in response to stimulation with extracellular ATP (100 μM). Cells remained untreated or were treated with 2-DG (2 mM), Rot (0.1 μM), Oligo (100 ng/ml), or FCCP (2 μM) 20 min before stimulation. Values are means ± SE from 3 independent experiments. ## P < 0.01. ### P < 0.001. * P < 0.05, ** P < 0.01, and *** P < 0.001 compared with ATP-treated cells. C : for migration assay, growth-arrested cells were seeded in Boyden chamber-permeable inserts and pretreated with the indicated for 20 min. ATP, MeSADP, or adenosine (Ado; 500 μM) were added to the lower compartment to initiate migration. Number of migrated cells was evaluated as described in methods . Values are means ± SE from 4 independent experiments. ### P < 0.001, control vs. ATP-stimulated cells. * P < 0.05, ** P < 0.01, and *** P < 0.01, untreated vs. treated with inhibitors.

Journal: American Journal of Physiology - Cell Physiology

Article Title: Glycolysis and oxidative phosphorylation are essential for purinergic receptor-mediated angiogenic responses in vasa vasorum endothelial cells

doi: 10.1152/ajpcell.00250.2016

Figure Lengend Snippet: Glycolysis and mitochondrial oxidative phosphorylation are necessary for VVEC proliferative and migratory responses. A : proliferation rates were determined in VVEC grown in DMEM/1% FBS in the presence of oligomycin (Oligo; 10 ng/ml), rotenone (Rot; 0.1 μM), 2-deoxyglucose (2-DG; 0.2 mM), and FCCP (0.5 μM) The media with indicated inhibitors were refreshed each second day. Cell proliferation rate was assessed using a fluorescent CyQuant proliferation kit. Values are means ± SE from 3 independent experiments. B : [ 3 H]thymidine incorporation was determined in growth-arrested VVEC (DMEM without serum, 72 h) in response to stimulation with extracellular ATP (100 μM). Cells remained untreated or were treated with 2-DG (2 mM), Rot (0.1 μM), Oligo (100 ng/ml), or FCCP (2 μM) 20 min before stimulation. Values are means ± SE from 3 independent experiments. ## P < 0.01. ### P < 0.001. * P < 0.05, ** P < 0.01, and *** P < 0.001 compared with ATP-treated cells. C : for migration assay, growth-arrested cells were seeded in Boyden chamber-permeable inserts and pretreated with the indicated for 20 min. ATP, MeSADP, or adenosine (Ado; 500 μM) were added to the lower compartment to initiate migration. Number of migrated cells was evaluated as described in methods . Values are means ± SE from 4 independent experiments. ### P < 0.001, control vs. ATP-stimulated cells. * P < 0.05, ** P < 0.01, and *** P < 0.01, untreated vs. treated with inhibitors.

Article Snippet: VVEC were cultured in glass-bottom dishes suitable for fluorescent imaging (MatTek, Ashland, MA) and growth-arrested in serum-free DMEM for 72 h before the experiments.

Techniques: Phospho-proteomics, CyQUANT Assay, Migration, Control