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tgf-β monoclonal mouse neutralizing antibody tgfmab clone 1d11  (Bio X Cell)


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    Bio X Cell tgf-β monoclonal mouse neutralizing antibody tgfmab clone 1d11
    Tgf β Monoclonal Mouse Neutralizing Antibody Tgfmab Clone 1d11, supplied by Bio X Cell, 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/tgf-%CE%B2+monoclonal+mouse+neutralizing+antibody/us12144805-976-22-25?v=Bio+X+Cell
    Average 90 stars, based on 1 article reviews
    tgf-β monoclonal mouse neutralizing antibody tgfmab clone 1d11 - by Bioz Stars, 2026-07
    90/100 stars

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    Fig. 3 AHR and inflammatory features of naive HFD and OVA-HFD models. AHR to MCh (a), inflammatory cell profile in the BALF (b), IL-4 (c) and IL-5 levels (d), and <t>TGF-β1</t> (e) concentrations in lung homogenates. Immunohistochemical staining for TGF-β1 (F) in tissue from naïve HFD, OVA-HFD, naive ND, and OVA-ND mice are shown. †P < 0.05; ‡P < 0.01; *P < 0.001. AHR airway hyperresponsiveness, MCh methacholine, BALF bronchoalveolar lavage fluid, HFD high-fat-diet, IL interleukin, OVA ovalbumin, ND normal diet, TGF transforming growth factor
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    Image Search Results


    Fig. 3 AHR and inflammatory features of naive HFD and OVA-HFD models. AHR to MCh (a), inflammatory cell profile in the BALF (b), IL-4 (c) and IL-5 levels (d), and TGF-β1 (e) concentrations in lung homogenates. Immunohistochemical staining for TGF-β1 (F) in tissue from naïve HFD, OVA-HFD, naive ND, and OVA-ND mice are shown. †P < 0.05; ‡P < 0.01; *P < 0.001. AHR airway hyperresponsiveness, MCh methacholine, BALF bronchoalveolar lavage fluid, HFD high-fat-diet, IL interleukin, OVA ovalbumin, ND normal diet, TGF transforming growth factor

    Journal: Experimental & molecular medicine

    Article Title: Insulin resistance mediates high-fat diet-induced pulmonary fibrosis and airway hyperresponsiveness through the TGF-β1 pathway.

    doi: 10.1038/s12276-019-0258-7

    Figure Lengend Snippet: Fig. 3 AHR and inflammatory features of naive HFD and OVA-HFD models. AHR to MCh (a), inflammatory cell profile in the BALF (b), IL-4 (c) and IL-5 levels (d), and TGF-β1 (e) concentrations in lung homogenates. Immunohistochemical staining for TGF-β1 (F) in tissue from naïve HFD, OVA-HFD, naive ND, and OVA-ND mice are shown. †P < 0.05; ‡P < 0.01; *P < 0.001. AHR airway hyperresponsiveness, MCh methacholine, BALF bronchoalveolar lavage fluid, HFD high-fat-diet, IL interleukin, OVA ovalbumin, ND normal diet, TGF transforming growth factor

    Article Snippet: To block TGF-β1, a rabbit anti-mouse TGF-β neutralizing mAb (100 μg/mouse; R&D Systems Inc., Minneapolis, MN, USA) or rabbit IgG antibody (100 μg/ mouse; R&D Systems) was administered once via the intravenous (i.v.) route 4 h before the first OVA challenge (Fig. 1).

    Techniques: Immunohistochemical staining, Staining

    Effects of exogenous EGF, TGF-β1, or TGF-β2 on the spreading of the corneal endothelium in organ culture. Exogenous EGF promoted endothelium spreading. While adding exogenous TGF-β1 (A) or TGF-β2 (B) to the medium exhibited no effect on endothelium sheet elongation, it counteracted the promotion of endothelial sheet elongation by exogenous EGF.

    Journal: Molecular Vision

    Article Title: Inhibitory effect of blocking TGF-β/Smad signal on injury-induced fibrosis of corneal endothelium

    doi:

    Figure Lengend Snippet: Effects of exogenous EGF, TGF-β1, or TGF-β2 on the spreading of the corneal endothelium in organ culture. Exogenous EGF promoted endothelium spreading. While adding exogenous TGF-β1 (A) or TGF-β2 (B) to the medium exhibited no effect on endothelium sheet elongation, it counteracted the promotion of endothelial sheet elongation by exogenous EGF.

    Article Snippet: To examine the role of endogenous TGF-β in endothelium spreading, the medium was supplemented with either mouse monoclonal anti-human TGF-β neutralizing antibody (20 μg/ml, R&D systems) or mouse IgG1 derived from BALB/c strain (20 μg/ml, Sigma-Aldrich).

    Techniques: Organ Culture

    The role of endogenous TGF-β was evaluated by using neutralizing antibody. Adding neutralizing anti-TGF-β antibody retarded endothelium repair.

    Journal: Molecular Vision

    Article Title: Inhibitory effect of blocking TGF-β/Smad signal on injury-induced fibrosis of corneal endothelium

    doi:

    Figure Lengend Snippet: The role of endogenous TGF-β was evaluated by using neutralizing antibody. Adding neutralizing anti-TGF-β antibody retarded endothelium repair.

    Article Snippet: To examine the role of endogenous TGF-β in endothelium spreading, the medium was supplemented with either mouse monoclonal anti-human TGF-β neutralizing antibody (20 μg/ml, R&D systems) or mouse IgG1 derived from BALB/c strain (20 μg/ml, Sigma-Aldrich).

    Techniques:

    Roles of TGF-β related signaling on the spreading of the corneal endothelium in organ culture. The p38 inhibitor, SB203580, and the MAPK inhibitor, U0126, hindered endothelium sheet elongation (inhibition: SB203580>U0126). Neither the JNK inhibitor nor the ALK5 inhibitor, SB431542, (blocking Smad2/3 signal) have a significant effect on its repair.

    Journal: Molecular Vision

    Article Title: Inhibitory effect of blocking TGF-β/Smad signal on injury-induced fibrosis of corneal endothelium

    doi:

    Figure Lengend Snippet: Roles of TGF-β related signaling on the spreading of the corneal endothelium in organ culture. The p38 inhibitor, SB203580, and the MAPK inhibitor, U0126, hindered endothelium sheet elongation (inhibition: SB203580>U0126). Neither the JNK inhibitor nor the ALK5 inhibitor, SB431542, (blocking Smad2/3 signal) have a significant effect on its repair.

    Article Snippet: To examine the role of endogenous TGF-β in endothelium spreading, the medium was supplemented with either mouse monoclonal anti-human TGF-β neutralizing antibody (20 μg/ml, R&D systems) or mouse IgG1 derived from BALB/c strain (20 μg/ml, Sigma-Aldrich).

    Techniques: Organ Culture, Inhibition, Blocking Assay