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monoclonal rabbit anti gr antibody  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc monoclonal rabbit anti gr antibody
    Endogenous AAT and GR co-localize in human PBMCs. Co-staining of adherent human blood PBMCs with anti-AAT ( red ) and polyclonal ( A ) or <t>monoclonal</t> ( B ) anti-GR ( green ) antibodies reveals co-localization of AAT and GR in the cytoplasm. Nuclei were stained with DAPI. Images were taken using a confocal laser scanning microscope (Olympus FluorView 1000) equipped with a 60× oil-immersion objective. Scale bars represent 20 μm
    Monoclonal Rabbit Anti Gr Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/antibody+rabbit+anti+gr/pmc13064270-124-57-61
    Average 86 stars, based on 1 article reviews
    monoclonal rabbit anti gr antibody - by Bioz Stars, 2026-10
    86/100 stars

    Images

    1) Product Images from "Alpha-1 antitrypsin–glucocorticoid receptor axis: a new pathway in immune modulation"

    Article Title: Alpha-1 antitrypsin–glucocorticoid receptor axis: a new pathway in immune modulation

    Journal: Molecular Medicine

    doi: 10.1186/s10020-026-01470-z

    Endogenous AAT and GR co-localize in human PBMCs. Co-staining of adherent human blood PBMCs with anti-AAT ( red ) and polyclonal ( A ) or monoclonal ( B ) anti-GR ( green ) antibodies reveals co-localization of AAT and GR in the cytoplasm. Nuclei were stained with DAPI. Images were taken using a confocal laser scanning microscope (Olympus FluorView 1000) equipped with a 60× oil-immersion objective. Scale bars represent 20 μm
    Figure Legend Snippet: Endogenous AAT and GR co-localize in human PBMCs. Co-staining of adherent human blood PBMCs with anti-AAT ( red ) and polyclonal ( A ) or monoclonal ( B ) anti-GR ( green ) antibodies reveals co-localization of AAT and GR in the cytoplasm. Nuclei were stained with DAPI. Images were taken using a confocal laser scanning microscope (Olympus FluorView 1000) equipped with a 60× oil-immersion objective. Scale bars represent 20 μm

    Techniques Used: Staining, Laser-Scanning Microscopy

    Related Articles

    Staining:

    Article Title: Phellopterin from angelica dahurica is a natural antagonist of glucocorticoid receptors regulating lipid and cholesterol metabolism.
    Article Snippet: Phellopterin, a compound isolated from Angelica dahurica, has broad-spectrum metabolic modulatory activities, including anti-inflammatory and lipid-lowering effects.. However, its molecular pharmacological mechanism and direct target are not fully understood.. Glucocorticoids (GCs) have been identified as important risk factors for metabolic syndromes such as obesity, hyperlipidemia and fatty liver.

    Article Title: Cedrol mitigates hepatic lipid accumulation and adipocyte hypertrophy induced by corticosteroids through the inhibition of glucocorticoid receptor activity.
    Article Snippet: .. Immunofluorescence staining was performed with the primary antibody rabbit anti-GR (CST) and secondary antibody goat anti-rabbit IgG (H+L) Cross-Adsorbed Alexa FluorTM 488 (A11008, Thermo Fisher Scientific, USA). ..

    Article Title: Cedrol mitigates hepatic lipid accumulation and adipocyte hypertrophy induced by corticosteroids through the inhibition of glucocorticoid receptor activity
    Article Snippet: .. Immunofluorescence staining was performed with the primary antibody rabbit anti-GR (CST) and secondary antibody goat anti-rabbit IgG (H + L) Cross-Adsorbed Alexa FluorTM 488 (A11008, Thermo Fisher Scientific, USA). ..

    Immunofluorescence:

    Article Title: Phellopterin from angelica dahurica is a natural antagonist of glucocorticoid receptors regulating lipid and cholesterol metabolism.
    Article Snippet: Phellopterin, a compound isolated from Angelica dahurica, has broad-spectrum metabolic modulatory activities, including anti-inflammatory and lipid-lowering effects.. However, its molecular pharmacological mechanism and direct target are not fully understood.. Glucocorticoids (GCs) have been identified as important risk factors for metabolic syndromes such as obesity, hyperlipidemia and fatty liver.

    Article Title: Cedrol mitigates hepatic lipid accumulation and adipocyte hypertrophy induced by corticosteroids through the inhibition of glucocorticoid receptor activity.
    Article Snippet: .. Immunofluorescence staining was performed with the primary antibody rabbit anti-GR (CST) and secondary antibody goat anti-rabbit IgG (H+L) Cross-Adsorbed Alexa FluorTM 488 (A11008, Thermo Fisher Scientific, USA). ..

    Article Title: Cedrol mitigates hepatic lipid accumulation and adipocyte hypertrophy induced by corticosteroids through the inhibition of glucocorticoid receptor activity
    Article Snippet: .. Immunofluorescence staining was performed with the primary antibody rabbit anti-GR (CST) and secondary antibody goat anti-rabbit IgG (H + L) Cross-Adsorbed Alexa FluorTM 488 (A11008, Thermo Fisher Scientific, USA). ..



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    Image Search Results


    Endogenous AAT and GR co-localize in human PBMCs. Co-staining of adherent human blood PBMCs with anti-AAT ( red ) and polyclonal ( A ) or monoclonal ( B ) anti-GR ( green ) antibodies reveals co-localization of AAT and GR in the cytoplasm. Nuclei were stained with DAPI. Images were taken using a confocal laser scanning microscope (Olympus FluorView 1000) equipped with a 60× oil-immersion objective. Scale bars represent 20 μm

    Journal: Molecular Medicine

    Article Title: Alpha-1 antitrypsin–glucocorticoid receptor axis: a new pathway in immune modulation

    doi: 10.1186/s10020-026-01470-z

    Figure Lengend Snippet: Endogenous AAT and GR co-localize in human PBMCs. Co-staining of adherent human blood PBMCs with anti-AAT ( red ) and polyclonal ( A ) or monoclonal ( B ) anti-GR ( green ) antibodies reveals co-localization of AAT and GR in the cytoplasm. Nuclei were stained with DAPI. Images were taken using a confocal laser scanning microscope (Olympus FluorView 1000) equipped with a 60× oil-immersion objective. Scale bars represent 20 μm

    Article Snippet: Adherent cells were fixed with 4% paraformaldehyde (PFA) for 10 min at 37 °C, permeabilized with 0.05% Triton-X100 for 5 min and blocked with 5% BSA in PBS for 1 h. AAT was stained with monoclonal mouse-anti AAT antibody (Proteintech, dilution 1:200) and GR was stained with polyclonal rabbit anti-GR antibody (Thermo Fisher Scientific, dilution 1:100) or monoclonal rabbit anti-GR antibody (Cell Signaling, dilution 1:200).

    Techniques: Staining, Laser-Scanning Microscopy