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anti gdf11 primary antibody  (R&D Systems)


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    R&D Systems anti gdf11 primary antibody
    Anti Gdf11 Primary Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 24 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/recombinant+gdf11/Recombinant+Human%2FMouse%2FRat+GDF-11%2FBMP-11+Protein/pm41637825-94-14-19
    Average 93 stars, based on 24 article reviews
    anti gdf11 primary antibody - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Recombinant:

    Article Title: GDF11 alleviates secondary brain injury after intracerebral hemorrhage via attenuating mitochondrial dynamic abnormality and dysfunction
    Article Snippet: .. IP injections of recombinant GDF11 (R&D Systems, catalog No.1958-GD-010) (0.1 mg/kg/day) or vehicle only (30 mM acetate) were first given 2 h prior to operation and daily continued until the end of this experiment (7 days after operation). ..

    Article Title: Hypoxia-induced miR-1260b regulates vascular smooth muscle cell proliferation by targeting GDF11
    Article Snippet: Cell culture Human primary pulmonary artery smooth muscle cells (PASMCs) were purchased from Lonza (CC-2581) and cultured as previously described (11). .. For hypoxia, PASMCs in Sm-Gm2 medium (Lonza) were grown in a sealed modular incubator chamber (Billups-rothenberg Inc.) for 24 h at 37C after flushing with a mixture of 5% CO2, 1% O2 and 94% N2 for 4 min. For GDF11 stimulation, 10 ng of recombinant GDF11 purchased from R&D Systems was used. .. Human primary pulmonary artery smooth muscle cells (PASMCs) were purchased from Lonza (CC-2581) and cultured as previously described (11).

    Article Title: Circulating α-Klotho Counteracts Transforming Growth Factor-β-Induced Sarcopenia.
    Article Snippet: From the Departments of Neurology,* Natural Sciences,z and Pathology,{ Kawasaki Medical School,zz Kurashiki; the Department of Health and Sports Science,y Faculty of Health Science and Technology, Kawasaki University of Medical Welfare, Kurashiki; the Department of Medical Science,x Teikyo University of Science, Tokyo; the Department of Animal and Marine Bioresource Sciences,k Graduate School of Agriculture, Kyushu University, Fukuoka; the Department of Food and Life Science,** School of Life and Environmental Science, Azabu University, Sagamihara; and the Research Coordination Group,yy Tokyo Research Park, R&D Division, Kyowa Kirin Co., Ltd., Tokyo, Japan

    Article Title: Growth Differentiation Factor 11 Evokes Lung Injury, Inflammation, and Fibrosis in Mice through the Activin A Receptor Type II-Like Kinase, 53kDa-Smad2/3 Signaling Pathway.
    Article Snippet: opyright a 2024 American Society for Inves echnologies. ttps://doi.org/10.1016/j.ajpath.2024.07.016 Growth differentiation factor 11 (GDF11) belongs to the transforming growth factor beta superfamily and participates in various pathophysiological processes.. Initially, GDF11 was suggested to act as a rejuvenator by improving age-related phenotypes of the heart, brain, and skeletal muscle in aged mice.. Recent studies demonstrate that GDF11 also serves as an adverse risk factor for human frailty and diseases.

    Article Title: Supraphysiological levels of GDF11 induce striated muscle atrophy.
    Article Snippet: .. At day 7 of differentiation, myotube cultures were separated into control (n = 5), 50 ng/ml recombinant Mstn (R&D Systems #788-G8; n = 4), 50 ng/ml recombinant GDF11 (R&D Systems #1958-GD; n = 5), or 50 ng/ml recombinant TGFb (R&D Systems #240-B; n = 3) enriched differentiation media for 72 h. All recombinant proteins were reconstituted according to the manufacturer’s instruction in 4 mM HCl with 0.1% bovine serum albumin (BSA). .. At day 10, cultures were fixed in 4% paraformaldehyde (PFA), permeabilized in 0.1% Triton X-100, and blocked in 0.2% BSA for 1 h. Myotubes were stained with anti-myosin heavy chain (clone MY-32; Sigma-Aldrich #M1570; St. Louis, MO) overnight, incubated with Alexa-568-conjugated goat anti-mouse secondary antibody (Life Technologies #A11031; Grand Island, NY) for 1 h, and counter stained with DAPI (Sigma-Aldrich).

    Article Title: Supraphysiological levels of GDF 11 induce striated muscle atrophy
    Article Snippet: .. At day 7 of differentiation, myotube cultures were separated into control ( n = 5), 50 ng/ml recombinant Mstn (R&D Systems #788‐G8; n = 4), 50 ng/ml recombinant GDF11 (R&D Systems #1958‐GD; n = 5), or 50 ng/ml recombinant TGFβ (R&D Systems #240‐B; n = 3) enriched differentiation media for 72 h. All recombinant proteins were reconstituted according to the manufacturer's instruction in 4 mM HCl with 0.1% bovine serum albumin (BSA). .. At day 10, cultures were fixed in 4% paraformaldehyde (PFA), permeabilized in 0.1% Triton X‐100, and blocked in 0.2% BSA for 1 h. Myotubes were stained with anti‐myosin heavy chain (clone MY‐32; Sigma‐Aldrich #M1570; St. Louis, MO) overnight, incubated with Alexa‐568‐conjugated goat anti‐mouse secondary antibody (Life Technologies #A11031; Grand Island, NY) for 1 h, and counter stained with DAPI (Sigma‐Aldrich).

    Article Title: Development of an ultra-sensitive Simoa assay to enable GDF11 detection: a comparison across bioanalytical platforms.
    Article Snippet: 2016 Background: Four bioanalytical platforms were evaluated to optimize sensitivity and enable detection of recombinant human GDF11 in biological matrices; ELISA, Meso Scale Discovery, Gyrolab xP Workstation and Simoa HD-1.. Results & methodology: After completion of custom assay development, the single-molecule ELISA (Simoa) achieved the greatest sensitivity with a lower limit of quantitation of 0.1 ng/ml, an improvement of 100-fold over the next sensitive platform (MSD).. Discussion & conclusion: This improvement was essential to enable detection of GDF11 in biological samples, and without the technology the sensitivity achieved on the other platforms would not have been sufficient.

    Article Title: Hypoxia-induced miR-1260b regulates vascular smooth muscle cell proliferation by targeting GDF11
    Article Snippet: Human primary pulmonary artery smooth muscle cells (PASMCs) were purchased from Lonza (CC-2581) and cultured as previously described (11). .. For hypoxia, PASMCs in Sm-Gm2 medium (Lonza) were grown in a sealed modular incubator chamber (Billups-rothenberg Inc.) for 24 h at 37oC after flushing with a mixture of 5% CO2, 1% O2 and 94% N2 for 4 min. For GDF11 stimulation, 10 ng of recombinant GDF11 purchased from R&D Systems was used. ..

    Modification:

    Article Title: Circulating α-Klotho Counteracts Transforming Growth Factor-β-Induced Sarcopenia.
    Article Snippet: From the Departments of Neurology,* Natural Sciences,z and Pathology,{ Kawasaki Medical School,zz Kurashiki; the Department of Health and Sports Science,y Faculty of Health Science and Technology, Kawasaki University of Medical Welfare, Kurashiki; the Department of Medical Science,x Teikyo University of Science, Tokyo; the Department of Animal and Marine Bioresource Sciences,k Graduate School of Agriculture, Kyushu University, Fukuoka; the Department of Food and Life Science,** School of Life and Environmental Science, Azabu University, Sagamihara; and the Research Coordination Group,yy Tokyo Research Park, R&D Division, Kyowa Kirin Co., Ltd., Tokyo, Japan

    Control:

    Article Title: Growth Differentiation Factor 11 Evokes Lung Injury, Inflammation, and Fibrosis in Mice through the Activin A Receptor Type II-Like Kinase, 53kDa-Smad2/3 Signaling Pathway.
    Article Snippet: opyright a 2024 American Society for Inves echnologies. ttps://doi.org/10.1016/j.ajpath.2024.07.016 Growth differentiation factor 11 (GDF11) belongs to the transforming growth factor beta superfamily and participates in various pathophysiological processes.. Initially, GDF11 was suggested to act as a rejuvenator by improving age-related phenotypes of the heart, brain, and skeletal muscle in aged mice.. Recent studies demonstrate that GDF11 also serves as an adverse risk factor for human frailty and diseases.

    Article Title: Supraphysiological levels of GDF11 induce striated muscle atrophy.
    Article Snippet: .. At day 7 of differentiation, myotube cultures were separated into control (n = 5), 50 ng/ml recombinant Mstn (R&D Systems #788-G8; n = 4), 50 ng/ml recombinant GDF11 (R&D Systems #1958-GD; n = 5), or 50 ng/ml recombinant TGFb (R&D Systems #240-B; n = 3) enriched differentiation media for 72 h. All recombinant proteins were reconstituted according to the manufacturer’s instruction in 4 mM HCl with 0.1% bovine serum albumin (BSA). .. At day 10, cultures were fixed in 4% paraformaldehyde (PFA), permeabilized in 0.1% Triton X-100, and blocked in 0.2% BSA for 1 h. Myotubes were stained with anti-myosin heavy chain (clone MY-32; Sigma-Aldrich #M1570; St. Louis, MO) overnight, incubated with Alexa-568-conjugated goat anti-mouse secondary antibody (Life Technologies #A11031; Grand Island, NY) for 1 h, and counter stained with DAPI (Sigma-Aldrich).

    Article Title: Supraphysiological levels of GDF 11 induce striated muscle atrophy
    Article Snippet: .. At day 7 of differentiation, myotube cultures were separated into control ( n = 5), 50 ng/ml recombinant Mstn (R&D Systems #788‐G8; n = 4), 50 ng/ml recombinant GDF11 (R&D Systems #1958‐GD; n = 5), or 50 ng/ml recombinant TGFβ (R&D Systems #240‐B; n = 3) enriched differentiation media for 72 h. All recombinant proteins were reconstituted according to the manufacturer's instruction in 4 mM HCl with 0.1% bovine serum albumin (BSA). .. At day 10, cultures were fixed in 4% paraformaldehyde (PFA), permeabilized in 0.1% Triton X‐100, and blocked in 0.2% BSA for 1 h. Myotubes were stained with anti‐myosin heavy chain (clone MY‐32; Sigma‐Aldrich #M1570; St. Louis, MO) overnight, incubated with Alexa‐568‐conjugated goat anti‐mouse secondary antibody (Life Technologies #A11031; Grand Island, NY) for 1 h, and counter stained with DAPI (Sigma‐Aldrich).

    Saline:

    Article Title: Growth Differentiation Factor 11 Evokes Lung Injury, Inflammation, and Fibrosis in Mice through the Activin A Receptor Type II-Like Kinase, 53kDa-Smad2/3 Signaling Pathway.
    Article Snippet: opyright a 2024 American Society for Inves echnologies. ttps://doi.org/10.1016/j.ajpath.2024.07.016 Growth differentiation factor 11 (GDF11) belongs to the transforming growth factor beta superfamily and participates in various pathophysiological processes.. Initially, GDF11 was suggested to act as a rejuvenator by improving age-related phenotypes of the heart, brain, and skeletal muscle in aged mice.. Recent studies demonstrate that GDF11 also serves as an adverse risk factor for human frailty and diseases.

    Binding Assay:

    Article Title: Development of an ultra-sensitive Simoa assay to enable GDF11 detection: a comparison across bioanalytical platforms.
    Article Snippet: 2016 Background: Four bioanalytical platforms were evaluated to optimize sensitivity and enable detection of recombinant human GDF11 in biological matrices; ELISA, Meso Scale Discovery, Gyrolab xP Workstation and Simoa HD-1.. Results & methodology: After completion of custom assay development, the single-molecule ELISA (Simoa) achieved the greatest sensitivity with a lower limit of quantitation of 0.1 ng/ml, an improvement of 100-fold over the next sensitive platform (MSD).. Discussion & conclusion: This improvement was essential to enable detection of GDF11 in biological samples, and without the technology the sensitivity achieved on the other platforms would not have been sufficient.



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    Figure 5 Myostatin-specific inhibition by myostatin-b. HeLa cells cotransfected with Luc and Gal plasmids were treated with recombinant myostatin at concentrations of 0, 20, 40 and 60 ng/mL (A); recombinant growth differentiation factor 11 <t>(GDF11)</t> at concentrations of 0, 10, 20 and 30 ng/mL (B); recombinant transforming growth factor β1 (TGF-β1) at concentrations of 0, 0.5, 1 and 2 ng/mL (C); and activin A at concentrations of 0, 10, 20 and 30 ng/mL (D). In addition, the myostatin-b plasmid was cotransfected into each treated cell. The results of luciferase activity are shown. Myostatin-b inhibited myostatin signalling induced only by recombinant myostatin but not by recombinant GDF11, recombinant TGF-β1 or recombinant activin A (red bars). The data are expressed as the mean ± SEM of three independent experiments. **P < 0.01, ***P < 0.001. RLU, relative luminescence unit.
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    Information of antibodies

    Journal: Journal of Neuroinflammation

    Article Title: Stabilizing histamine release in gut mast cells mitigates peripheral and central inflammation after stroke

    doi: 10.1186/s12974-023-02887-7

    Figure Lengend Snippet: Information of antibodies

    Article Snippet: Recombinant Human GDF11 protein (ab50159) , abcam ab50159 , 1:1000.

    Techniques: Recombinant

    Figure 5 Myostatin-specific inhibition by myostatin-b. HeLa cells cotransfected with Luc and Gal plasmids were treated with recombinant myostatin at concentrations of 0, 20, 40 and 60 ng/mL (A); recombinant growth differentiation factor 11 (GDF11) at concentrations of 0, 10, 20 and 30 ng/mL (B); recombinant transforming growth factor β1 (TGF-β1) at concentrations of 0, 0.5, 1 and 2 ng/mL (C); and activin A at concentrations of 0, 10, 20 and 30 ng/mL (D). In addition, the myostatin-b plasmid was cotransfected into each treated cell. The results of luciferase activity are shown. Myostatin-b inhibited myostatin signalling induced only by recombinant myostatin but not by recombinant GDF11, recombinant TGF-β1 or recombinant activin A (red bars). The data are expressed as the mean ± SEM of three independent experiments. **P < 0.01, ***P < 0.001. RLU, relative luminescence unit.

    Journal: Journal of cachexia, sarcopenia and muscle

    Article Title: A novel splice variant of the human MSTN gene encodes a myostatin-specific myostatin inhibitor.

    doi: 10.1002/jcsm.13314

    Figure Lengend Snippet: Figure 5 Myostatin-specific inhibition by myostatin-b. HeLa cells cotransfected with Luc and Gal plasmids were treated with recombinant myostatin at concentrations of 0, 20, 40 and 60 ng/mL (A); recombinant growth differentiation factor 11 (GDF11) at concentrations of 0, 10, 20 and 30 ng/mL (B); recombinant transforming growth factor β1 (TGF-β1) at concentrations of 0, 0.5, 1 and 2 ng/mL (C); and activin A at concentrations of 0, 10, 20 and 30 ng/mL (D). In addition, the myostatin-b plasmid was cotransfected into each treated cell. The results of luciferase activity are shown. Myostatin-b inhibited myostatin signalling induced only by recombinant myostatin but not by recombinant GDF11, recombinant TGF-β1 or recombinant activin A (red bars). The data are expressed as the mean ± SEM of three independent experiments. **P < 0.01, ***P < 0.001. RLU, relative luminescence unit.

    Article Snippet: After 24 h, the medium was replaced with serum-free RPMI 1640 or DMEM containing recombinant myostatin (788-G8, R&D Systems), recombinant growth differentiation factor 11 (GDF11) (1958-GD, R&D Systems), recombinant TGF-β1 (240-B/CF, R&D Systems) or recombinant activin A (338-AC/CF, R&D Systems).

    Techniques: Inhibition, Recombinant, Plasmid Preparation, Luciferase, Activity Assay