clc3 Search Results


anti clc-3  (Alomone Labs)
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Alomone Labs anti clc-3
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clc3  (Santa Cruz Biotechnology)
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Santa Cruz Biotechnology clc3
Clc3, supplied by Santa Cruz Biotechnology, 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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sirna oligonucleotides against clc 3  (Santa Cruz Biotechnology)
88
Santa Cruz Biotechnology sirna oligonucleotides against clc 3
Sirna Oligonucleotides Against Clc 3, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rabbit anti-rat clcn1  (Alpha Diagnostics)
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Alpha Diagnostics rabbit anti-rat clcn1
Rabbit Anti Rat Clcn1, supplied by Alpha Diagnostics, 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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tat-clc-3 107−116 (ygrkkrrqrrr-inskkkesaw  (GenScript corporation)
90
GenScript corporation tat-clc-3 107−116 (ygrkkrrqrrr-inskkkesaw
Tat Clc 3 107−116 (Ygrkkrrqrrr Inskkkesaw, supplied by GenScript corporation, 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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sirna clc-3  (Shanghai GenePharma)
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Shanghai GenePharma sirna clc-3
Sirna Clc 3, supplied by Shanghai GenePharma, 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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anti-clc-3 antibody  (Blackwell Science Ltd)
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Blackwell Science Ltd anti-clc-3 antibody
Anti Clc 3 Antibody, supplied by Blackwell Science Ltd, 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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pmrfp-clc3  (Institut Curie)
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Institut Curie pmrfp-clc3
Pmrfp Clc3, supplied by Institut Curie, 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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monoclonal antibody to clc-3  (NeuroMab)
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NeuroMab monoclonal antibody to clc-3
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adenovirus (ad)-clc-3 shrna  (SunBio Inc)
90
SunBio Inc adenovirus (ad)-clc-3 shrna
Effects of ClC-3 on Ang II-induced ROS production in HUVECs. a Ang II treatment increased ClC-3 expression in HUVECs (*P < 0.05 vs. CON. n = 5). b and c Effects of adenovirus (Ad)-ClC-3 shRNA and Ad-ClC-3 <t>transfection</t> on the expression of ClC-3 in HUVECs. Cells were transfected with Ad-ClC-3 shRNA (100 MOI) (b) or Ad-ClC-3 (100 MOI) (c) for 48 h (*P < 0.05 vs. CON. n = 4). d and e Representative images (× 400) with quantitative analysis of the dihydroethidium (DHE) fluorescence intensity (in arbitrary units) were shown in HUVECs transfected with Ad-ClC-3 shRNA (d) or Ad-ClC-3 (e) upon stimulation with Ang II (1 μmol/L) for 24 h. Ang II-induced ROS production was attenuated by knockdown of ClC-3, and further enhanced by ClC-3 overexpression (n = 6, **P < 0.01 vs. CON, ##P < 0.01 vs. Ang II). f ClC-3 potentiated Ang II-induced senescence of HUVECs. HUVECs were transfected with Ad-ClC-3 shRNA or Ad-ClC-3 for 48 h and then were incubated with or without Ang II (1 μmol/L) for 24 h. Representative photomicrographs (× 400) show the senescence-associated β-galactosidase (SA-β-Gal)-positive cells with different treatments (n = 6)
Adenovirus (Ad) Clc 3 Shrna, supplied by SunBio Inc, 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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plasmid of mouse clc-3, splice variant c  (Forschungszentrum gmbh)
90
Forschungszentrum gmbh plasmid of mouse clc-3, splice variant c
Effects of ClC-3 on Ang II-induced ROS production in HUVECs. a Ang II treatment increased ClC-3 expression in HUVECs (*P < 0.05 vs. CON. n = 5). b and c Effects of adenovirus (Ad)-ClC-3 shRNA and Ad-ClC-3 <t>transfection</t> on the expression of ClC-3 in HUVECs. Cells were transfected with Ad-ClC-3 shRNA (100 MOI) (b) or Ad-ClC-3 (100 MOI) (c) for 48 h (*P < 0.05 vs. CON. n = 4). d and e Representative images (× 400) with quantitative analysis of the dihydroethidium (DHE) fluorescence intensity (in arbitrary units) were shown in HUVECs transfected with Ad-ClC-3 shRNA (d) or Ad-ClC-3 (e) upon stimulation with Ang II (1 μmol/L) for 24 h. Ang II-induced ROS production was attenuated by knockdown of ClC-3, and further enhanced by ClC-3 overexpression (n = 6, **P < 0.01 vs. CON, ##P < 0.01 vs. Ang II). f ClC-3 potentiated Ang II-induced senescence of HUVECs. HUVECs were transfected with Ad-ClC-3 shRNA or Ad-ClC-3 for 48 h and then were incubated with or without Ang II (1 μmol/L) for 24 h. Representative photomicrographs (× 400) show the senescence-associated β-galactosidase (SA-β-Gal)-positive cells with different treatments (n = 6)
Plasmid Of Mouse Clc 3, Splice Variant C, supplied by Forschungszentrum gmbh, 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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tat-clc-3 scr  (GenScript corporation)
90
GenScript corporation tat-clc-3 scr
Effects of ClC-3 on Ang II-induced ROS production in HUVECs. a Ang II treatment increased ClC-3 expression in HUVECs (*P < 0.05 vs. CON. n = 5). b and c Effects of adenovirus (Ad)-ClC-3 shRNA and Ad-ClC-3 <t>transfection</t> on the expression of ClC-3 in HUVECs. Cells were transfected with Ad-ClC-3 shRNA (100 MOI) (b) or Ad-ClC-3 (100 MOI) (c) for 48 h (*P < 0.05 vs. CON. n = 4). d and e Representative images (× 400) with quantitative analysis of the dihydroethidium (DHE) fluorescence intensity (in arbitrary units) were shown in HUVECs transfected with Ad-ClC-3 shRNA (d) or Ad-ClC-3 (e) upon stimulation with Ang II (1 μmol/L) for 24 h. Ang II-induced ROS production was attenuated by knockdown of ClC-3, and further enhanced by ClC-3 overexpression (n = 6, **P < 0.01 vs. CON, ##P < 0.01 vs. Ang II). f ClC-3 potentiated Ang II-induced senescence of HUVECs. HUVECs were transfected with Ad-ClC-3 shRNA or Ad-ClC-3 for 48 h and then were incubated with or without Ang II (1 μmol/L) for 24 h. Representative photomicrographs (× 400) show the senescence-associated β-galactosidase (SA-β-Gal)-positive cells with different treatments (n = 6)
Tat Clc 3 Scr, supplied by GenScript corporation, 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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Image Search Results


Effects of ClC-3 on Ang II-induced ROS production in HUVECs. a Ang II treatment increased ClC-3 expression in HUVECs (*P < 0.05 vs. CON. n = 5). b and c Effects of adenovirus (Ad)-ClC-3 shRNA and Ad-ClC-3 transfection on the expression of ClC-3 in HUVECs. Cells were transfected with Ad-ClC-3 shRNA (100 MOI) (b) or Ad-ClC-3 (100 MOI) (c) for 48 h (*P < 0.05 vs. CON. n = 4). d and e Representative images (× 400) with quantitative analysis of the dihydroethidium (DHE) fluorescence intensity (in arbitrary units) were shown in HUVECs transfected with Ad-ClC-3 shRNA (d) or Ad-ClC-3 (e) upon stimulation with Ang II (1 μmol/L) for 24 h. Ang II-induced ROS production was attenuated by knockdown of ClC-3, and further enhanced by ClC-3 overexpression (n = 6, **P < 0.01 vs. CON, ##P < 0.01 vs. Ang II). f ClC-3 potentiated Ang II-induced senescence of HUVECs. HUVECs were transfected with Ad-ClC-3 shRNA or Ad-ClC-3 for 48 h and then were incubated with or without Ang II (1 μmol/L) for 24 h. Representative photomicrographs (× 400) show the senescence-associated β-galactosidase (SA-β-Gal)-positive cells with different treatments (n = 6)

Journal: Acta Pharmacologica Sinica

Article Title: ClC-3 promotes angiotensin II-induced reactive oxygen species production in endothelial cells by facilitating Nox2 NADPH oxidase complex formation

doi: 10.1038/s41401-018-0072-0

Figure Lengend Snippet: Effects of ClC-3 on Ang II-induced ROS production in HUVECs. a Ang II treatment increased ClC-3 expression in HUVECs (*P < 0.05 vs. CON. n = 5). b and c Effects of adenovirus (Ad)-ClC-3 shRNA and Ad-ClC-3 transfection on the expression of ClC-3 in HUVECs. Cells were transfected with Ad-ClC-3 shRNA (100 MOI) (b) or Ad-ClC-3 (100 MOI) (c) for 48 h (*P < 0.05 vs. CON. n = 4). d and e Representative images (× 400) with quantitative analysis of the dihydroethidium (DHE) fluorescence intensity (in arbitrary units) were shown in HUVECs transfected with Ad-ClC-3 shRNA (d) or Ad-ClC-3 (e) upon stimulation with Ang II (1 μmol/L) for 24 h. Ang II-induced ROS production was attenuated by knockdown of ClC-3, and further enhanced by ClC-3 overexpression (n = 6, **P < 0.01 vs. CON, ##P < 0.01 vs. Ang II). f ClC-3 potentiated Ang II-induced senescence of HUVECs. HUVECs were transfected with Ad-ClC-3 shRNA or Ad-ClC-3 for 48 h and then were incubated with or without Ang II (1 μmol/L) for 24 h. Representative photomicrographs (× 400) show the senescence-associated β-galactosidase (SA-β-Gal)-positive cells with different treatments (n = 6)

Article Snippet: Adenovirus transfection Adenovirus (Ad)-ClC-3 shRNA and Ad-ClC-3 cDNA were designed and produced by Sunbio Medical Biotechnology (Shanghai, China).

Techniques: Expressing, shRNA, Transfection, Fluorescence, Knockdown, Over Expression, Incubation

ClC-3 increased p47phox phosphorylation through p38 MAPK pathway. a The time course of p47phox and p38 MAPK phosphorylation in Ang II-treated HUVECs (n = 5, *P < 0.05 vs. CON, **P < 0.01 vs. CON). b Knockdown of ClC-3 decreased p38 MAPK phosphorylation induced by Ang II (1 μmol/L) treatment for 30 min. c Overexpression of ClC-3 enhanced p38 MAPK phosphorylation (n = 5, *P < 0.05 vs. CON, #P < 0.05 vs. Ang II). d–f Cells were pretreated with the p38 MAPK inhibitor SB203580 (10 μmol/L) for 6 h before Ad-ClC-3 transfection. SB203580 abolished the increase in p47phox phosphorylation (d), NADPH oxidase activity (e), and ROS generation (f) induced by ClC-3 overexpression in HUVECs with Ang II treatment, respectively (n = 6, **P < 0.01 vs. Ang II, ##P < 0.01 vs. Ang II+Ad-ClC-3)

Journal: Acta Pharmacologica Sinica

Article Title: ClC-3 promotes angiotensin II-induced reactive oxygen species production in endothelial cells by facilitating Nox2 NADPH oxidase complex formation

doi: 10.1038/s41401-018-0072-0

Figure Lengend Snippet: ClC-3 increased p47phox phosphorylation through p38 MAPK pathway. a The time course of p47phox and p38 MAPK phosphorylation in Ang II-treated HUVECs (n = 5, *P < 0.05 vs. CON, **P < 0.01 vs. CON). b Knockdown of ClC-3 decreased p38 MAPK phosphorylation induced by Ang II (1 μmol/L) treatment for 30 min. c Overexpression of ClC-3 enhanced p38 MAPK phosphorylation (n = 5, *P < 0.05 vs. CON, #P < 0.05 vs. Ang II). d–f Cells were pretreated with the p38 MAPK inhibitor SB203580 (10 μmol/L) for 6 h before Ad-ClC-3 transfection. SB203580 abolished the increase in p47phox phosphorylation (d), NADPH oxidase activity (e), and ROS generation (f) induced by ClC-3 overexpression in HUVECs with Ang II treatment, respectively (n = 6, **P < 0.01 vs. Ang II, ##P < 0.01 vs. Ang II+Ad-ClC-3)

Article Snippet: Adenovirus transfection Adenovirus (Ad)-ClC-3 shRNA and Ad-ClC-3 cDNA were designed and produced by Sunbio Medical Biotechnology (Shanghai, China).

Techniques: Phospho-proteomics, Knockdown, Over Expression, Transfection, Activity Assay