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anti tgf β  (R&D Systems)


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    Structured Review

    R&D Systems anti tgf β
    Anti Tgf β, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 201 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tgf+%CE%B2+1+2+3+antibody/TGF-beta+1%2C+2%2C+3+Antibody/bio_rxiv__64898__2026__02__12__705496-173-26-28
    Average 95 stars, based on 201 article reviews
    anti tgf β - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    Inhibition:

    Article Title: Polyol Pathway Links Glucose Metabolism to the Aggressiveness of Cancer Cells
    Article Snippet: In vitro treatments For EMT induction, cells were treated with 10 ng/ml TGF-β (R&D Systems) for 2-3 days or with 50 or 100 mM glucose (Sigma) for 3-6 days. .. Inhibition of TGF-β signaling was performed with a neutralizing TGF-β 1,2,3 antibody (R&D systems, 1D11, 1 μg/ml) in the presence of either 11 mM (concentration of standard Research. on January 17, 2018. ..

    Concentration Assay:

    Article Title: Polyol Pathway Links Glucose Metabolism to the Aggressiveness of Cancer Cells
    Article Snippet: In vitro treatments For EMT induction, cells were treated with 10 ng/ml TGF-β (R&D Systems) for 2-3 days or with 50 or 100 mM glucose (Sigma) for 3-6 days. .. Inhibition of TGF-β signaling was performed with a neutralizing TGF-β 1,2,3 antibody (R&D systems, 1D11, 1 μg/ml) in the presence of either 11 mM (concentration of standard Research. on January 17, 2018. ..



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    R&D Systems mouse α tgf β mab
    TNF-α tumor necrosis factor-α, IFN-ϒ interferon-ϒ, IL-23 interleukin 23, <t>TGF-β1</t> transforming growth factor β1, TGF-β2 transforming growth factor β2. a En face atherosclerosis assay showing significantly less atherosclerosis in fortilin KO-MΦ-HC mice than in fortilin WT-MΦ-HC mice. b Cross-sectional atherosclerosis assay showing significantly less atherosclerosis in fortilin KO-MΦ-HC mice than in fortilin WT-MΦ-HC mice. Quantitative multiplex cytokine assays of ( c ) TNF-α, ( d ) IFN-ϒ, ( e ) IL-23, ( f ) TGFβ-1, and ( g ) TGF-β2. The scale bar in ( b ) equals 100 µm. Data are expressed as mean ± s.d., P values were determined by either two-sided Student’s t test ( a , b , f , g ) or two-tailed Mann–Whitney test ( c , d , e ).
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    TNF-α tumor necrosis factor-α, IFN-ϒ interferon-ϒ, IL-23 interleukin 23, <t>TGF-β1</t> transforming growth factor β1, TGF-β2 transforming growth factor β2. a En face atherosclerosis assay showing significantly less atherosclerosis in fortilin KO-MΦ-HC mice than in fortilin WT-MΦ-HC mice. b Cross-sectional atherosclerosis assay showing significantly less atherosclerosis in fortilin KO-MΦ-HC mice than in fortilin WT-MΦ-HC mice. Quantitative multiplex cytokine assays of ( c ) TNF-α, ( d ) IFN-ϒ, ( e ) IL-23, ( f ) TGFβ-1, and ( g ) TGF-β2. The scale bar in ( b ) equals 100 µm. Data are expressed as mean ± s.d., P values were determined by either two-sided Student’s t test ( a , b , f , g ) or two-tailed Mann–Whitney test ( c , d , e ).
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    Image Search Results


    TNF-α tumor necrosis factor-α, IFN-ϒ interferon-ϒ, IL-23 interleukin 23, TGF-β1 transforming growth factor β1, TGF-β2 transforming growth factor β2. a En face atherosclerosis assay showing significantly less atherosclerosis in fortilin KO-MΦ-HC mice than in fortilin WT-MΦ-HC mice. b Cross-sectional atherosclerosis assay showing significantly less atherosclerosis in fortilin KO-MΦ-HC mice than in fortilin WT-MΦ-HC mice. Quantitative multiplex cytokine assays of ( c ) TNF-α, ( d ) IFN-ϒ, ( e ) IL-23, ( f ) TGFβ-1, and ( g ) TGF-β2. The scale bar in ( b ) equals 100 µm. Data are expressed as mean ± s.d., P values were determined by either two-sided Student’s t test ( a , b , f , g ) or two-tailed Mann–Whitney test ( c , d , e ).

    Journal: Communications Biology

    Article Title: Fortilin deficiency induces anti-atherosclerotic phenotypes in macrophages and protects hypercholesterolemic mice against atherosclerosis

    doi: 10.1038/s42003-025-08425-w

    Figure Lengend Snippet: TNF-α tumor necrosis factor-α, IFN-ϒ interferon-ϒ, IL-23 interleukin 23, TGF-β1 transforming growth factor β1, TGF-β2 transforming growth factor β2. a En face atherosclerosis assay showing significantly less atherosclerosis in fortilin KO-MΦ-HC mice than in fortilin WT-MΦ-HC mice. b Cross-sectional atherosclerosis assay showing significantly less atherosclerosis in fortilin KO-MΦ-HC mice than in fortilin WT-MΦ-HC mice. Quantitative multiplex cytokine assays of ( c ) TNF-α, ( d ) IFN-ϒ, ( e ) IL-23, ( f ) TGFβ-1, and ( g ) TGF-β2. The scale bar in ( b ) equals 100 µm. Data are expressed as mean ± s.d., P values were determined by either two-sided Student’s t test ( a , b , f , g ) or two-tailed Mann–Whitney test ( c , d , e ).

    Article Snippet: We first covalently coupled mouse α-TGF-β mAb (R&D Systems, Minneapolis, MN, USA; Clone 1D11, Catalog #: MAB1835-100) to tosylactivated magnetic beads (Dynabeads® M-280; Thermo Fisher, Catalog #: 14203) following manufacturer’s instructions.

    Techniques: Multiplex Assay, Two Tailed Test, MANN-WHITNEY

    CM conditioned media, WT THP1 WT-fortilin cells, KO THP1 KO-fortilin cells, oxLDL oxidized low density lipoprotein, UCDMSCs human umbilical cord derived mesenchymal stem cells, M media, F.C. fold change, α-TGF-β1-MB anti-TGF-β1-antibody-coated magnetic beads, ID-CM CM immunodepleted of TGF-β1, TGF-β1 ID media with TGF-β1 immunodepleted of TGF-β1. Time-course of RT-qPCR of RNA from UCDMSCs treated by either M only, M + TGF-β1, CM of THP1 KO-fortilin , or CM of THP1 WT-fortilin ( a ) for VSMC markers (αSMA ( b ); SM22α ( c ); and CNN1 ( d )), a differentiation marker (CD45; e ); and a marker of undifferentiated cells (CD105, f ) (n = 3 for each group). g ELISA of CM from THP1 WT-fortilin cells and THP1 KO-fortilin cells with and without oxLDL stimulation (n = 4 for each group). RT-qPCR of RNA from UCDMSCs treated by either M only with and without TGF-β1 ID, M + TGF-β1 with and without TGF-β1 ID, CM of THP1 KO-fortilin with and without TGF-β1 ID, or CM of THP1 WT-fortilin with and without TGF-β1 ID ( h ) for VSMC markers αSMA ( i ), SM22α ( j ), and CNN1 ( k ); a differentiation marker (CD45, l ); and a marker of undifferentiated cells (CD105, m ) (n = 3 for each group). Data are expressed as mean ± s.d. P values determined by one way ANOVA ( b – g , i – m ) are shown.

    Journal: Communications Biology

    Article Title: Fortilin deficiency induces anti-atherosclerotic phenotypes in macrophages and protects hypercholesterolemic mice against atherosclerosis

    doi: 10.1038/s42003-025-08425-w

    Figure Lengend Snippet: CM conditioned media, WT THP1 WT-fortilin cells, KO THP1 KO-fortilin cells, oxLDL oxidized low density lipoprotein, UCDMSCs human umbilical cord derived mesenchymal stem cells, M media, F.C. fold change, α-TGF-β1-MB anti-TGF-β1-antibody-coated magnetic beads, ID-CM CM immunodepleted of TGF-β1, TGF-β1 ID media with TGF-β1 immunodepleted of TGF-β1. Time-course of RT-qPCR of RNA from UCDMSCs treated by either M only, M + TGF-β1, CM of THP1 KO-fortilin , or CM of THP1 WT-fortilin ( a ) for VSMC markers (αSMA ( b ); SM22α ( c ); and CNN1 ( d )), a differentiation marker (CD45; e ); and a marker of undifferentiated cells (CD105, f ) (n = 3 for each group). g ELISA of CM from THP1 WT-fortilin cells and THP1 KO-fortilin cells with and without oxLDL stimulation (n = 4 for each group). RT-qPCR of RNA from UCDMSCs treated by either M only with and without TGF-β1 ID, M + TGF-β1 with and without TGF-β1 ID, CM of THP1 KO-fortilin with and without TGF-β1 ID, or CM of THP1 WT-fortilin with and without TGF-β1 ID ( h ) for VSMC markers αSMA ( i ), SM22α ( j ), and CNN1 ( k ); a differentiation marker (CD45, l ); and a marker of undifferentiated cells (CD105, m ) (n = 3 for each group). Data are expressed as mean ± s.d. P values determined by one way ANOVA ( b – g , i – m ) are shown.

    Article Snippet: We first covalently coupled mouse α-TGF-β mAb (R&D Systems, Minneapolis, MN, USA; Clone 1D11, Catalog #: MAB1835-100) to tosylactivated magnetic beads (Dynabeads® M-280; Thermo Fisher, Catalog #: 14203) following manufacturer’s instructions.

    Techniques: Derivative Assay, Magnetic Beads, Quantitative RT-PCR, Marker, Enzyme-linked Immunosorbent Assay

    FT fortilin, MΦ macrophages, VSMCs vascular smooth muscle cells, MSCs mesenchymal stem cells. The lack of fortilin in MΦ produces profound phenotypic changes, making MΦ anti-atherosclerotic. More specifically, fortilin deficiency in MΦ suppresses their proliferation and FC formation, but promotes their apoptosis, TGF-β1 secretion, and transdifferentiation into VSMCs, and also drives MSC differentiation into VSMCs via TGF-β1 ( b ), compared with normal fortilin expression ( a ).

    Journal: Communications Biology

    Article Title: Fortilin deficiency induces anti-atherosclerotic phenotypes in macrophages and protects hypercholesterolemic mice against atherosclerosis

    doi: 10.1038/s42003-025-08425-w

    Figure Lengend Snippet: FT fortilin, MΦ macrophages, VSMCs vascular smooth muscle cells, MSCs mesenchymal stem cells. The lack of fortilin in MΦ produces profound phenotypic changes, making MΦ anti-atherosclerotic. More specifically, fortilin deficiency in MΦ suppresses their proliferation and FC formation, but promotes their apoptosis, TGF-β1 secretion, and transdifferentiation into VSMCs, and also drives MSC differentiation into VSMCs via TGF-β1 ( b ), compared with normal fortilin expression ( a ).

    Article Snippet: We first covalently coupled mouse α-TGF-β mAb (R&D Systems, Minneapolis, MN, USA; Clone 1D11, Catalog #: MAB1835-100) to tosylactivated magnetic beads (Dynabeads® M-280; Thermo Fisher, Catalog #: 14203) following manufacturer’s instructions.

    Techniques: Expressing