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mouse monoclonal anti human pparγ2  (R&D Systems)


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    R&D Systems mouse monoclonal anti human pparγ2
    Biotinylated DNA oligo capture and PPARγ IP in different cellular environments of ΔL1 cells. A, PPARγ IP in the cytoplasm and nucleus following 4-day ligand treatment using mouse monoclonal anti-human PPARγ antibody (m_hPPARγ). IgG control is shown in the middle. B, and C, 3× DR1 biotinylated oligo capture in the nucleus and cytoplasm following 1-day ligand treatment, respectively. D) PPARγ IP in the nucleus following 1-day treatment. The SDS-PAGE gels were transferred to nitrocellulose and proteins were visualized using rabbit polyclonal anti-human PPARγ antibody (r_hPPARγ), and a fluorescent labeled secondary antibody from rabbit to detect the respective IgG isotype. Band A indicates endogeneous PPARγ from ΔL1 cells where band B denotes human Flag-tagged <t>PPARγ2</t> transfected in the HEK_293T cells. The arrow that is marked with a (?) is likely because of cross-reactivity with the antibody rather than PPARγ1 isoform. WBs were processed and analyzed using Licor Technology.
    Mouse Monoclonal Anti Human Pparγ2, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pp+k8450b+00/Human+PPAR+gamma+2%2FNR1C3+Antibody+(Clone+K8450B)/pmc05724174-56-39-52
    Average 90 stars, based on 2 article reviews
    mouse monoclonal anti human pparγ2 - by Bioz Stars, 2026-10
    90/100 stars

    Images

    1) Product Images from "Unique Interactome Network Signatures for Peroxisome Proliferator-activated Receptor Gamma (PPARγ) Modulation by Functional Selective Ligands "

    Article Title: Unique Interactome Network Signatures for Peroxisome Proliferator-activated Receptor Gamma (PPARγ) Modulation by Functional Selective Ligands

    Journal: Molecular & Cellular Proteomics : MCP

    doi: 10.1074/mcp.RA117.000308

    Biotinylated DNA oligo capture and PPARγ IP in different cellular environments of ΔL1 cells. A, PPARγ IP in the cytoplasm and nucleus following 4-day ligand treatment using mouse monoclonal anti-human PPARγ antibody (m_hPPARγ). IgG control is shown in the middle. B, and C, 3× DR1 biotinylated oligo capture in the nucleus and cytoplasm following 1-day ligand treatment, respectively. D) PPARγ IP in the nucleus following 1-day treatment. The SDS-PAGE gels were transferred to nitrocellulose and proteins were visualized using rabbit polyclonal anti-human PPARγ antibody (r_hPPARγ), and a fluorescent labeled secondary antibody from rabbit to detect the respective IgG isotype. Band A indicates endogeneous PPARγ from ΔL1 cells where band B denotes human Flag-tagged PPARγ2 transfected in the HEK_293T cells. The arrow that is marked with a (?) is likely because of cross-reactivity with the antibody rather than PPARγ1 isoform. WBs were processed and analyzed using Licor Technology.
    Figure Legend Snippet: Biotinylated DNA oligo capture and PPARγ IP in different cellular environments of ΔL1 cells. A, PPARγ IP in the cytoplasm and nucleus following 4-day ligand treatment using mouse monoclonal anti-human PPARγ antibody (m_hPPARγ). IgG control is shown in the middle. B, and C, 3× DR1 biotinylated oligo capture in the nucleus and cytoplasm following 1-day ligand treatment, respectively. D) PPARγ IP in the nucleus following 1-day treatment. The SDS-PAGE gels were transferred to nitrocellulose and proteins were visualized using rabbit polyclonal anti-human PPARγ antibody (r_hPPARγ), and a fluorescent labeled secondary antibody from rabbit to detect the respective IgG isotype. Band A indicates endogeneous PPARγ from ΔL1 cells where band B denotes human Flag-tagged PPARγ2 transfected in the HEK_293T cells. The arrow that is marked with a (?) is likely because of cross-reactivity with the antibody rather than PPARγ1 isoform. WBs were processed and analyzed using Licor Technology.

    Techniques Used: Control, SDS Page, Labeling, Transfection

    Related Articles

    Immunostaining:

    Article Title: Chemerin, a Novel Peroxisome Proliferator-activated Receptor ? (PPAR?) Target Gene That Promotes Mesenchymal Stem Cell Adipogenesis
    Article Snippet: .. Immunostaining of the blots was performed using goat anti-chemerin (1:1000) (catalogue number AF2325, R&D Systems) or mouse anti-adiponectin (1:5000) (catalogue number MAB3604, Chemicon), mouse anti-cyclin A2 (1:1000) (catalogue number AF5999, R&D Systems), mouse anti-cyclin B2 (1:1000) (catalogue number AF6004, R&D Systems), mouse anti-cyclin D2 (1:1000) (catalogue number AF4196, R&D Systems), mouse anti-PPARγ (1:1000) (catalogue number PP-K8450B-00, R&D Systems), and mouse anti-β-actin (1:1000) (catalogue number ab8226, Abcam). .. The appropriate secondary antibodies conjugated with a 680 nm infrared fluorophore (LI-COR Biosciences, Lincoln, NE) were used at 1:10,000 dilution.

    Article Title: Chemerin, a Novel Peroxisome Proliferator-activated Receptor γ (PPARγ) Target Gene That Promotes Mesenchymal Stem Cell Adipogenesis
    Article Snippet: .. Immunostaining of the blots was performed using goat antichemerin (1:1000) (catalogue number AF2325, R&D Systems) or mouse anti-adiponectin (1:5000) (catalogue number MAB3604, Chemicon), mouse anti-cyclin A2 (1:1000) (catalogue number AF5999, R&D Systems), mouse anti-cyclin B2 (1:1000) (catalogue number AF6004, R&D Systems), mouse anti-cyclin D2 (1:1000) (catalogue number AF4196, R&D Systems), mouse anti-PPAR (1:1000) (catalogue number PP-K8450B-00, R&D Systems), and mouse anti- -actin (1:1000) (catalogue number ab8226, Abcam). .. The appropriate secondary antibodies conjugated with a 680 nm infrared fluorophore (LI-COR Biosciences, Lincoln, NE) were used at 1:10,000 dilution.



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    Biotinylated DNA oligo capture and PPARγ IP in different cellular environments of ΔL1 cells. A, PPARγ IP in the cytoplasm and nucleus following 4-day ligand treatment using mouse monoclonal anti-human PPARγ antibody (m_hPPARγ). IgG control is shown in the middle. B, and C, 3× DR1 biotinylated oligo capture in the nucleus and cytoplasm following 1-day ligand treatment, respectively. D) PPARγ IP in the nucleus following 1-day treatment. The SDS-PAGE gels were transferred to nitrocellulose and proteins were visualized using rabbit polyclonal anti-human PPARγ antibody (r_hPPARγ), and a fluorescent labeled secondary antibody from rabbit to detect the respective IgG isotype. Band A indicates endogeneous PPARγ from ΔL1 cells where band B denotes human Flag-tagged <t>PPARγ2</t> transfected in the HEK_293T cells. The arrow that is marked with a (?) is likely because of cross-reactivity with the antibody rather than PPARγ1 isoform. WBs were processed and analyzed using Licor Technology.
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    Image Search Results


    Biotinylated DNA oligo capture and PPARγ IP in different cellular environments of ΔL1 cells. A, PPARγ IP in the cytoplasm and nucleus following 4-day ligand treatment using mouse monoclonal anti-human PPARγ antibody (m_hPPARγ). IgG control is shown in the middle. B, and C, 3× DR1 biotinylated oligo capture in the nucleus and cytoplasm following 1-day ligand treatment, respectively. D) PPARγ IP in the nucleus following 1-day treatment. The SDS-PAGE gels were transferred to nitrocellulose and proteins were visualized using rabbit polyclonal anti-human PPARγ antibody (r_hPPARγ), and a fluorescent labeled secondary antibody from rabbit to detect the respective IgG isotype. Band A indicates endogeneous PPARγ from ΔL1 cells where band B denotes human Flag-tagged PPARγ2 transfected in the HEK_293T cells. The arrow that is marked with a (?) is likely because of cross-reactivity with the antibody rather than PPARγ1 isoform. WBs were processed and analyzed using Licor Technology.

    Journal: Molecular & Cellular Proteomics : MCP

    Article Title: Unique Interactome Network Signatures for Peroxisome Proliferator-activated Receptor Gamma (PPARγ) Modulation by Functional Selective Ligands

    doi: 10.1074/mcp.RA117.000308

    Figure Lengend Snippet: Biotinylated DNA oligo capture and PPARγ IP in different cellular environments of ΔL1 cells. A, PPARγ IP in the cytoplasm and nucleus following 4-day ligand treatment using mouse monoclonal anti-human PPARγ antibody (m_hPPARγ). IgG control is shown in the middle. B, and C, 3× DR1 biotinylated oligo capture in the nucleus and cytoplasm following 1-day ligand treatment, respectively. D) PPARγ IP in the nucleus following 1-day treatment. The SDS-PAGE gels were transferred to nitrocellulose and proteins were visualized using rabbit polyclonal anti-human PPARγ antibody (r_hPPARγ), and a fluorescent labeled secondary antibody from rabbit to detect the respective IgG isotype. Band A indicates endogeneous PPARγ from ΔL1 cells where band B denotes human Flag-tagged PPARγ2 transfected in the HEK_293T cells. The arrow that is marked with a (?) is likely because of cross-reactivity with the antibody rather than PPARγ1 isoform. WBs were processed and analyzed using Licor Technology.

    Article Snippet: Primary mouse monoclonal anti-human PPARγ (sc-7273; 408–505; Lot#: L3013) for IP, rabbit polyclonal anti-human PPARγ (sc-7196; 8–108; Lot#: A2512) for Western blot (WB), and mouse IgG (sc-2025; Lot#: C1915) were purchased from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA) Mouse monoclonal anti-human PPARγ2 (PP-K8450B-00; 1–28; Lot#: A-2) for WB was obtained from R&D Systems (Minneapolis, MN).

    Techniques: Control, SDS Page, Labeling, Transfection