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control adenovirus expressing gfp (ad-empty vector)  (Vigene Biosciences)

 
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    Structured Review

    Vigene Biosciences control adenovirus expressing gfp (ad-empty vector)
    Over-activation of STAT3 attenuated the inhibitory effects of CSR on RA-FLS hyperproliferation. RA-FLS were transduced with Ad-STAT3C (RA-FLS STAT3C ) or Ad-Empty (RA-FLS Empty vector ) plasmid. ( a ) <t>Green</t> <t>fluorescent</t> protein <t>(GFP)</t> expression and the protein levels of phospho-STAT3 (Tyr 705), STAT3 and Flag in RA-FLS Empty vector and RA-FLS STAT3C . Cells expressing GFP displayed green fluorescence. Representative green fluorescent and bright-field microscopy images of RA-FLS Empty vector and RA-FLS STAT3C are shown in the left panel (Scale bar: 10 μm). Representative immunoblotting results are shown in the right panel. Each membrane was cut based on molecular weights of proteins to be examined before hybridisation with primary antibodies. Original images of all blots are presented in Additional file . ( b ) Over-activation of STAT3 attenuated the inhibitory effect of CSR on RA-FLS hyperproliferation. Transduced RA-FLS were incubated with indicated concentrations of CSR for 1 h and then stimulated with IL-6/sIL-6R (100 ng/ml each) for 48 h. Cell viability was assessed using CCK-8 assays. Data are expressed as mean ± SD of 3 independent experiments. Differences of relative cell viabilities between CSR-treated RA-FLS Empty vector and CSR-treated RA-FLS STAT3C were calculated. * P < 0.05, ** P < 0.01
    Control Adenovirus Expressing Gfp (Ad Empty Vector), supplied by Vigene Biosciences, 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/empty+gfp-control+vector/recombinant+adenovirus+ad+gfp/pmc08928618-76-9-18
    Average 90 stars, based on 1 article reviews
    control adenovirus expressing gfp (ad-empty vector) - by Bioz Stars, 2026-11
    90/100 stars

    Images

    1) Product Images from "Chrysoeriol suppresses hyperproliferation of rheumatoid arthritis fibroblast-like synoviocytes and inhibits JAK2/STAT3 signaling"

    Article Title: Chrysoeriol suppresses hyperproliferation of rheumatoid arthritis fibroblast-like synoviocytes and inhibits JAK2/STAT3 signaling

    Journal: BMC Complementary Medicine and Therapies

    doi: 10.1186/s12906-022-03553-w

    Over-activation of STAT3 attenuated the inhibitory effects of CSR on RA-FLS hyperproliferation. RA-FLS were transduced with Ad-STAT3C (RA-FLS STAT3C ) or Ad-Empty (RA-FLS Empty vector ) plasmid. ( a ) Green fluorescent protein (GFP) expression and the protein levels of phospho-STAT3 (Tyr 705), STAT3 and Flag in RA-FLS Empty vector and RA-FLS STAT3C . Cells expressing GFP displayed green fluorescence. Representative green fluorescent and bright-field microscopy images of RA-FLS Empty vector and RA-FLS STAT3C are shown in the left panel (Scale bar: 10 μm). Representative immunoblotting results are shown in the right panel. Each membrane was cut based on molecular weights of proteins to be examined before hybridisation with primary antibodies. Original images of all blots are presented in Additional file . ( b ) Over-activation of STAT3 attenuated the inhibitory effect of CSR on RA-FLS hyperproliferation. Transduced RA-FLS were incubated with indicated concentrations of CSR for 1 h and then stimulated with IL-6/sIL-6R (100 ng/ml each) for 48 h. Cell viability was assessed using CCK-8 assays. Data are expressed as mean ± SD of 3 independent experiments. Differences of relative cell viabilities between CSR-treated RA-FLS Empty vector and CSR-treated RA-FLS STAT3C were calculated. * P < 0.05, ** P < 0.01
    Figure Legend Snippet: Over-activation of STAT3 attenuated the inhibitory effects of CSR on RA-FLS hyperproliferation. RA-FLS were transduced with Ad-STAT3C (RA-FLS STAT3C ) or Ad-Empty (RA-FLS Empty vector ) plasmid. ( a ) Green fluorescent protein (GFP) expression and the protein levels of phospho-STAT3 (Tyr 705), STAT3 and Flag in RA-FLS Empty vector and RA-FLS STAT3C . Cells expressing GFP displayed green fluorescence. Representative green fluorescent and bright-field microscopy images of RA-FLS Empty vector and RA-FLS STAT3C are shown in the left panel (Scale bar: 10 μm). Representative immunoblotting results are shown in the right panel. Each membrane was cut based on molecular weights of proteins to be examined before hybridisation with primary antibodies. Original images of all blots are presented in Additional file . ( b ) Over-activation of STAT3 attenuated the inhibitory effect of CSR on RA-FLS hyperproliferation. Transduced RA-FLS were incubated with indicated concentrations of CSR for 1 h and then stimulated with IL-6/sIL-6R (100 ng/ml each) for 48 h. Cell viability was assessed using CCK-8 assays. Data are expressed as mean ± SD of 3 independent experiments. Differences of relative cell viabilities between CSR-treated RA-FLS Empty vector and CSR-treated RA-FLS STAT3C were calculated. * P < 0.05, ** P < 0.01

    Techniques Used: Activation Assay, Transduction, Plasmid Preparation, Expressing, Fluorescence, Microscopy, Western Blot, Hybridization, Incubation, CCK-8 Assay

    Related Articles

    other:

    Article Title: HMGA1 regulates the mitochondrial apoptosis pathway in sepsis-induced cardiomyopathy.
    Article Snippet: Adenovirus carrying wild-type HMGA1 gene (Ad-HMGA1) and green fluorescent protein (Ad-GFP) were generated from Vigene Bioscience (Shandong, China).

    Article Title: Adrenomedullin gene delivery rescues estrogen production in Leydig cells via the inhibition of TGF-β1/Smads signaling pathway.
    Article Snippet: Our previous findings demonstrated that adrenomedullin (ADM) protects against the reduction in testosterone production and apoptosis of Leydig cells both in vitro and in vivo.. In this study, we investigated whether ADM could preserve estrogen production in Leydig cells by suppressing the transforming growth factor-β1 (TGF-β1) / Smads signaling pathway.. Leydig cells were treated with lipopolysaccharide (LPS) and recombinant adenovirus ADM (Ad-ADM), an adeno-associated viral vector expressing ADM.

    Over Expression:

    Article Title: Inhibition of xanthine oxidase alleviated pancreatic necrosis via HIF-1 α -regulated LDHA and NLRP3 signaling pathway in acute pancreatitis
    Article Snippet: .. For adenovirus-mediated overexpression, adenoviruses expressing Xdh and control green fluorescent protein were obtained from Vigene Bioscience (Jinan, China). ..

    Expressing:

    Article Title: Inhibition of xanthine oxidase alleviated pancreatic necrosis via HIF-1 α -regulated LDHA and NLRP3 signaling pathway in acute pancreatitis
    Article Snippet: .. For adenovirus-mediated overexpression, adenoviruses expressing Xdh and control green fluorescent protein were obtained from Vigene Bioscience (Jinan, China). ..

    Control:

    Article Title: Inhibition of xanthine oxidase alleviated pancreatic necrosis via HIF-1 α -regulated LDHA and NLRP3 signaling pathway in acute pancreatitis
    Article Snippet: .. For adenovirus-mediated overexpression, adenoviruses expressing Xdh and control green fluorescent protein were obtained from Vigene Bioscience (Jinan, China). ..

    Recombinant:

    Article Title: Calycosin reduces myocardial fibrosis and improves cardiac function in post-myocardial infarction mice by suppressing TGFBR1 signaling pathways.
    Article Snippet: Background: Excessive myocardial fibrosis is the pathological basis of heart failure following myocardial infarction (MI).. Although calycosin improves cardiac function, its effect on cardiac fibrosis and cardiac function after MI in mice and its precise mechanism remain unclear.. Purpose: Here, we firstly investigated the effects of calycosin on cardiac fibrosis and ventricular function in mice after MI and the role of transforming growth factor-beta receptor 1 (TGFBR1) signaling in the amelioration of cardiac fibrosis and ventricular function.

    Generated:

    Article Title: Calycosin reduces myocardial fibrosis and improves cardiac function in post-myocardial infarction mice by suppressing TGFBR1 signaling pathways.
    Article Snippet: Background: Excessive myocardial fibrosis is the pathological basis of heart failure following myocardial infarction (MI).. Although calycosin improves cardiac function, its effect on cardiac fibrosis and cardiac function after MI in mice and its precise mechanism remain unclear.. Purpose: Here, we firstly investigated the effects of calycosin on cardiac fibrosis and ventricular function in mice after MI and the role of transforming growth factor-beta receptor 1 (TGFBR1) signaling in the amelioration of cardiac fibrosis and ventricular function.

    Amplification:

    Article Title: Calycosin reduces myocardial fibrosis and improves cardiac function in post-myocardial infarction mice by suppressing TGFBR1 signaling pathways.
    Article Snippet: Background: Excessive myocardial fibrosis is the pathological basis of heart failure following myocardial infarction (MI).. Although calycosin improves cardiac function, its effect on cardiac fibrosis and cardiac function after MI in mice and its precise mechanism remain unclear.. Purpose: Here, we firstly investigated the effects of calycosin on cardiac fibrosis and ventricular function in mice after MI and the role of transforming growth factor-beta receptor 1 (TGFBR1) signaling in the amelioration of cardiac fibrosis and ventricular function.

    Transfection:

    Article Title: SIRT3 attenuates coronary atherosclerosis in diabetic patients by regulating endothelial cell function.
    Article Snippet: This is an open access article under the terms of the Creative Commons AttributionNonCommercialNoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is noncommercial and no modifications or adaptations are made.. © 2022 The Authors.. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC.



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    Image Search Results


    Key resources table

    Journal: iScience

    Article Title: The transcription factor IRF4 determines the anti-tumor immunity of CD8 + T cells

    doi: 10.1016/j.isci.2023.108087

    Figure Lengend Snippet: Key resources table

    Article Snippet: The retroviral particles were generated by transfecting plat-E cells with the IRF4-GFP vector or the empty GFP-control vector, following the manufacturer's instructions (Cell Biolabs).

    Techniques: Virus, Plasmid Preparation, Recombinant, Staining, Software

    Over-activation of STAT3 attenuated the inhibitory effects of CSR on RA-FLS hyperproliferation. RA-FLS were transduced with Ad-STAT3C (RA-FLS STAT3C ) or Ad-Empty (RA-FLS Empty vector ) plasmid. ( a ) Green fluorescent protein (GFP) expression and the protein levels of phospho-STAT3 (Tyr 705), STAT3 and Flag in RA-FLS Empty vector and RA-FLS STAT3C . Cells expressing GFP displayed green fluorescence. Representative green fluorescent and bright-field microscopy images of RA-FLS Empty vector and RA-FLS STAT3C are shown in the left panel (Scale bar: 10 μm). Representative immunoblotting results are shown in the right panel. Each membrane was cut based on molecular weights of proteins to be examined before hybridisation with primary antibodies. Original images of all blots are presented in Additional file . ( b ) Over-activation of STAT3 attenuated the inhibitory effect of CSR on RA-FLS hyperproliferation. Transduced RA-FLS were incubated with indicated concentrations of CSR for 1 h and then stimulated with IL-6/sIL-6R (100 ng/ml each) for 48 h. Cell viability was assessed using CCK-8 assays. Data are expressed as mean ± SD of 3 independent experiments. Differences of relative cell viabilities between CSR-treated RA-FLS Empty vector and CSR-treated RA-FLS STAT3C were calculated. * P < 0.05, ** P < 0.01

    Journal: BMC Complementary Medicine and Therapies

    Article Title: Chrysoeriol suppresses hyperproliferation of rheumatoid arthritis fibroblast-like synoviocytes and inhibits JAK2/STAT3 signaling

    doi: 10.1186/s12906-022-03553-w

    Figure Lengend Snippet: Over-activation of STAT3 attenuated the inhibitory effects of CSR on RA-FLS hyperproliferation. RA-FLS were transduced with Ad-STAT3C (RA-FLS STAT3C ) or Ad-Empty (RA-FLS Empty vector ) plasmid. ( a ) Green fluorescent protein (GFP) expression and the protein levels of phospho-STAT3 (Tyr 705), STAT3 and Flag in RA-FLS Empty vector and RA-FLS STAT3C . Cells expressing GFP displayed green fluorescence. Representative green fluorescent and bright-field microscopy images of RA-FLS Empty vector and RA-FLS STAT3C are shown in the left panel (Scale bar: 10 μm). Representative immunoblotting results are shown in the right panel. Each membrane was cut based on molecular weights of proteins to be examined before hybridisation with primary antibodies. Original images of all blots are presented in Additional file . ( b ) Over-activation of STAT3 attenuated the inhibitory effect of CSR on RA-FLS hyperproliferation. Transduced RA-FLS were incubated with indicated concentrations of CSR for 1 h and then stimulated with IL-6/sIL-6R (100 ng/ml each) for 48 h. Cell viability was assessed using CCK-8 assays. Data are expressed as mean ± SD of 3 independent experiments. Differences of relative cell viabilities between CSR-treated RA-FLS Empty vector and CSR-treated RA-FLS STAT3C were calculated. * P < 0.05, ** P < 0.01

    Article Snippet: Adenovirus expressing green fluorescent protein (GFP)-flag-tagged STAT3C (Ad-STAT3C) and control adenovirus expressing GFP (Ad-Empty vector) were purchased from Vigene Biosciences (Shandong, China).

    Techniques: Activation Assay, Transduction, Plasmid Preparation, Expressing, Fluorescence, Microscopy, Western Blot, Hybridization, Incubation, CCK-8 Assay

    Over-activation of STAT3 diminishes the inhibitory effects of Rg3-plus-ART on cell viability in HepG2-SR cells. HepG2-SR cells were transduced with the Ad-Empty vector (HepG2-SR Empty vector ) or the Ad-STAT3C plasmid (HepG2-SR STAT3C ). (A) GFP expression and the protein levels of STAT3, phospho-STAT3 (Tyr 705) and Flag in HepG2-SR Empty vector and HepG2-SR STAT3C cells. Representative green fluorescent and bright-field microscopy images of HepG2-SR Empty vector and HepG2-SR STAT3C (the left panel, scale bar, 10 μm), and representative immunoblotting results (the right panel) are shown. (B) Over-activation of STAT3 diminishes the anti-proliferative effects of Rg3-plus-ART in HepG2-SR cells. Differences of relative cell viabilities between Rg3-plus-ART-treated HepG2-SR Empty vector cells and Rg3-plus-ART-treated HepG2-SR STAT3C cells were calculated (n = 3). ∗ P < 0.05, ∗∗ P < 0.01.

    Journal: Journal of Ginseng Research

    Article Title: Ginsenoside Rg3 in combination with artesunate overcomes sorafenib resistance in hepatoma cell and mouse models

    doi: 10.1016/j.jgr.2021.07.002

    Figure Lengend Snippet: Over-activation of STAT3 diminishes the inhibitory effects of Rg3-plus-ART on cell viability in HepG2-SR cells. HepG2-SR cells were transduced with the Ad-Empty vector (HepG2-SR Empty vector ) or the Ad-STAT3C plasmid (HepG2-SR STAT3C ). (A) GFP expression and the protein levels of STAT3, phospho-STAT3 (Tyr 705) and Flag in HepG2-SR Empty vector and HepG2-SR STAT3C cells. Representative green fluorescent and bright-field microscopy images of HepG2-SR Empty vector and HepG2-SR STAT3C (the left panel, scale bar, 10 μm), and representative immunoblotting results (the right panel) are shown. (B) Over-activation of STAT3 diminishes the anti-proliferative effects of Rg3-plus-ART in HepG2-SR cells. Differences of relative cell viabilities between Rg3-plus-ART-treated HepG2-SR Empty vector cells and Rg3-plus-ART-treated HepG2-SR STAT3C cells were calculated (n = 3). ∗ P < 0.05, ∗∗ P < 0.01.

    Article Snippet: Adenovirus expressing GFP (green fluorescent protein)-Flag-tagged STAT3C (Ad-STAT3C) and control adenovirus expressing GFP (Ad-Empty vector) were purchased from Vigene Biosciences (Shandong, China).

    Techniques: Activation Assay, Transduction, Plasmid Preparation, Expressing, Microscopy, Western Blot