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heregulin-1β (hrg  (PeproTech)

 
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    PeproTech heregulin-1β (hrg
    Heregulin 1β (Hrg, supplied by PeproTech, 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/result/heregulin-1β (hrg/product/PeproTech
    Average 90 stars, based on 1 article reviews
    heregulin-1β (hrg - by Bioz Stars, 2026-03
    90/100 stars

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    BrdU assay of canine ( a , c , e ) and murine ( b , d , f ) satellite glial cells (SGCs) supplemented with fibroblast growth factor 2 (FGF), epidermal growth factor, (EGF), ciliary neurotrophic factor (CNTF), heregulin 1β (HRG), and forskolin (Fors). ( a , b ) Graphs show the percentage of BrdU + SGCs with and without supplementation. ( c – f ) Immunofluorescence BrdU labelling (green) of SGCs with bisbenzimide as nuclear counterstain. ( c , d ) control medium. ( e , f ) FGF supplementation. ** P < 0.01. *** P < 0.001. Bars, 60 μm. Shown are means with standard errors of the mean (SEM).

    Journal: Scientific Reports

    Article Title: Canine dorsal root ganglia satellite glial cells represent an exceptional cell population with astrocytic and oligodendrocytic properties

    doi: 10.1038/s41598-017-14246-7

    Figure Lengend Snippet: BrdU assay of canine ( a , c , e ) and murine ( b , d , f ) satellite glial cells (SGCs) supplemented with fibroblast growth factor 2 (FGF), epidermal growth factor, (EGF), ciliary neurotrophic factor (CNTF), heregulin 1β (HRG), and forskolin (Fors). ( a , b ) Graphs show the percentage of BrdU + SGCs with and without supplementation. ( c – f ) Immunofluorescence BrdU labelling (green) of SGCs with bisbenzimide as nuclear counterstain. ( c , d ) control medium. ( e , f ) FGF supplementation. ** P < 0.01. *** P < 0.001. Bars, 60 μm. Shown are means with standard errors of the mean (SEM).

    Article Snippet: The proliferation rate of SGCs (passage 2) supplemented with fibroblast growth factor 2 (FGF-2, 40 ng/ml; recombinant human, Peprotech, Hamburg, Germany), epidermal growth factor (EGF, 40 ng/ml; R&D Systems, Wiesbaden-Nordenstadt, Germany), ciliary neurotrophic factor (CNTF; 40 ng/ml; Peprotec), heregulin 1β (HRG-1β, 40 ng/ml; R&D Systems), and the cAMP-elevator forskolin (4 µM; F6886; Sigma-Aldrich) was evaluated.

    Techniques: BrdU Staining, Immunofluorescence, Control

    Apoptosis assay of canine ( a , c , e ) and murine ( b , d , f ) satellite glial cells (SGCs) supplemented with fibroblast growth factor 2 (FGF), epidermal growth factor, (EGF), ciliary neurotrophic factor (CNTF), heregulin 1β (HRG), and forskolin (Fors). ( a , b ) Graphs show the percentage of caspase-3 + SGCs with and without supplementation. ( c – f ) Immunofluorescence caspase-3 labelling (green) of SGCs with bisbenzimide as nuclear counterstain. ( c , d ) control medium. ( e , f ) FGF supplementation. * P < 0.05. ** P < 0.01. *** P < 0.001. Bars, 60 μm. Shown are means with standard errors of the mean (SEM).

    Journal: Scientific Reports

    Article Title: Canine dorsal root ganglia satellite glial cells represent an exceptional cell population with astrocytic and oligodendrocytic properties

    doi: 10.1038/s41598-017-14246-7

    Figure Lengend Snippet: Apoptosis assay of canine ( a , c , e ) and murine ( b , d , f ) satellite glial cells (SGCs) supplemented with fibroblast growth factor 2 (FGF), epidermal growth factor, (EGF), ciliary neurotrophic factor (CNTF), heregulin 1β (HRG), and forskolin (Fors). ( a , b ) Graphs show the percentage of caspase-3 + SGCs with and without supplementation. ( c – f ) Immunofluorescence caspase-3 labelling (green) of SGCs with bisbenzimide as nuclear counterstain. ( c , d ) control medium. ( e , f ) FGF supplementation. * P < 0.05. ** P < 0.01. *** P < 0.001. Bars, 60 μm. Shown are means with standard errors of the mean (SEM).

    Article Snippet: The proliferation rate of SGCs (passage 2) supplemented with fibroblast growth factor 2 (FGF-2, 40 ng/ml; recombinant human, Peprotech, Hamburg, Germany), epidermal growth factor (EGF, 40 ng/ml; R&D Systems, Wiesbaden-Nordenstadt, Germany), ciliary neurotrophic factor (CNTF; 40 ng/ml; Peprotec), heregulin 1β (HRG-1β, 40 ng/ml; R&D Systems), and the cAMP-elevator forskolin (4 µM; F6886; Sigma-Aldrich) was evaluated.

    Techniques: Apoptosis Assay, Immunofluorescence, Control

    GFAP expression of canine ( a , c , e ) and murine ( b , d , f ) satellite glial cells (SGCs) supplemented with fibroblast growth factor 2 (FGF), epidermal growth factor, (EGF), ciliary neurotrophic factor (CNTF), heregulin 1β (HRG), and forskolin (Fors). ( a , b ) Graphs show the percentage of glial fibrillary acidic protein (GFAP) + SGCs with and without supplementation. ( c – f ) Immunofluorescence double-labelling of SGCs for 2′,3′-cyclic-nucleotide 3′-phosphodiesterase (CNPase; red) and GFAP (green) with bisbenzimide as nuclear counterstain. ( c , d ) control medium. ( e , f ) FGF supplementation. * P < 0.05. *** P < 0.001. Bars, 60 μm. Shown are means with standard errors of the mean (SEM).

    Journal: Scientific Reports

    Article Title: Canine dorsal root ganglia satellite glial cells represent an exceptional cell population with astrocytic and oligodendrocytic properties

    doi: 10.1038/s41598-017-14246-7

    Figure Lengend Snippet: GFAP expression of canine ( a , c , e ) and murine ( b , d , f ) satellite glial cells (SGCs) supplemented with fibroblast growth factor 2 (FGF), epidermal growth factor, (EGF), ciliary neurotrophic factor (CNTF), heregulin 1β (HRG), and forskolin (Fors). ( a , b ) Graphs show the percentage of glial fibrillary acidic protein (GFAP) + SGCs with and without supplementation. ( c – f ) Immunofluorescence double-labelling of SGCs for 2′,3′-cyclic-nucleotide 3′-phosphodiesterase (CNPase; red) and GFAP (green) with bisbenzimide as nuclear counterstain. ( c , d ) control medium. ( e , f ) FGF supplementation. * P < 0.05. *** P < 0.001. Bars, 60 μm. Shown are means with standard errors of the mean (SEM).

    Article Snippet: The proliferation rate of SGCs (passage 2) supplemented with fibroblast growth factor 2 (FGF-2, 40 ng/ml; recombinant human, Peprotech, Hamburg, Germany), epidermal growth factor (EGF, 40 ng/ml; R&D Systems, Wiesbaden-Nordenstadt, Germany), ciliary neurotrophic factor (CNTF; 40 ng/ml; Peprotec), heregulin 1β (HRG-1β, 40 ng/ml; R&D Systems), and the cAMP-elevator forskolin (4 µM; F6886; Sigma-Aldrich) was evaluated.

    Techniques: Expressing, Immunofluorescence, Control