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anti il 2rβ  (Bio X Cell)


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    Structured Review

    Bio X Cell anti il 2rβ
    Anti Il 2rβ, supplied by Bio X Cell, used in various techniques. Bioz Stars score: 94/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+il+2r%CE%B2/InVivoMAb+anti-mouse+CD122/pm41844634-256-35-37
    Average 94 stars, based on 10 article reviews
    anti il 2rβ - by Bioz Stars, 2026-10
    94/100 stars

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    Article Title: Hexahydrocurcumin ameliorates hypertensive and vascular remodeling in L-NAME-induced rats.
    Article Snippet: 1 Introduction Increased levels of tumor-infiltrating lymphocytes (TILs) are associated with improved survival in patients with cancer (1–3).. Anti– PD-1/PD-L1–based cancer immunotherapies have revolutionized the treatment of cancers (4–8), and TIL abundance can be used as a prediction marker for immunotherapy responsiveness (9, 10).. Even though PD-1/PD-L1 blockade can release the brake on the T cell response, T cells are not fully functional and are limitedly expanded in the tumor (11, 12).

    Article Title: Reactivating exhausted tumor-infiltrating T cells by a bispecific DC-T cell engager in mice.
    Article Snippet: Antibodies used in this study included anti-CD4 (GK1.5, Bioxcell #BE0003-1), anti-CD8 (53-5.8, Bioxcell #BE0004-1), anti-NK1.1 (PK136, Bioxcell #BE0036), anti-CSF1R (AFS98, Bioxcell #BE0213), anti-IFN-γ (XMG1.2, Bioxcell #BE0050), anti-CD80 (16-10A1, Bioxcell, #BE0024), anti-CD86 (GL-1, Bioxcell, #BE0025), and anti-IL-2Rβ (TM-β1, Bioxcell, #BE0298), all purchased from Bio X Cell.



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    Bio X Cell invivomab anti mouse cd122 il 2rβ
    pH-responsive blocking and restoration of IL-2 receptor binding by UPS 5.3 (A) Schematic of the experimental design to assess the intrinsic interaction between UPS 5.3 micelles and proteins. (B) FPLC chromatograms showing individual proteins or UPS 5.3 /protein mixtures. (C) Molecular docking model of the DBA dimer (blue) with IL-2, highlighting predicted interaction sites. (D–F) Biolayer interferometry analysis of IL-2-Fc binding to IL-2Rα, <t>IL-2Rβ,</t> and IL-2Rγ, with and without UPS 5.3 NP encapsulation. (G) Schematic illustrating ex vivo assessment of IL-2-Fc binding to immune cells from various organs. (H) Quantification of IL-2-Fc binding to lymphocytes isolated from liver, lung, spleen, and tumor ( n = 5). Data are presented as mean ± SEM. See also and .
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    pH-responsive blocking and restoration of IL-2 receptor binding by UPS 5.3 (A) Schematic of the experimental design to assess the intrinsic interaction between UPS 5.3 micelles and proteins. (B) FPLC chromatograms showing individual proteins or UPS 5.3 /protein mixtures. (C) Molecular docking model of the DBA dimer (blue) with IL-2, highlighting predicted interaction sites. (D–F) Biolayer interferometry analysis of IL-2-Fc binding to IL-2Rα, <t>IL-2Rβ,</t> and IL-2Rγ, with and without UPS 5.3 NP encapsulation. (G) Schematic illustrating ex vivo assessment of IL-2-Fc binding to immune cells from various organs. (H) Quantification of IL-2-Fc binding to lymphocytes isolated from liver, lung, spleen, and tumor ( n = 5). Data are presented as mean ± SEM. See also and .
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    pH-responsive blocking and restoration of IL-2 receptor binding by UPS 5.3 (A) Schematic of the experimental design to assess the intrinsic interaction between UPS 5.3 micelles and proteins. (B) FPLC chromatograms showing individual proteins or UPS 5.3 /protein mixtures. (C) Molecular docking model of the DBA dimer (blue) with IL-2, highlighting predicted interaction sites. (D–F) Biolayer interferometry analysis of IL-2-Fc binding to IL-2Rα, <t>IL-2Rβ,</t> and IL-2Rγ, with and without UPS 5.3 NP encapsulation. (G) Schematic illustrating ex vivo assessment of IL-2-Fc binding to immune cells from various organs. (H) Quantification of IL-2-Fc binding to lymphocytes isolated from liver, lung, spleen, and tumor ( n = 5). Data are presented as mean ± SEM. See also and .
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    Santa Cruz Biotechnology il 2rβ
    Expression of <t>IL-2Rα,</t> <t>IL-2Rβ,</t> and IL-2Rγ subunits in renal cell carcinoma cells, demonstrated by PCR products on an agarose gel. Representative blot with relative quantification shows IL-2Rα, IL-2Rβ, and IL-2Rγ protein detection in A-498, ACHN, Caki-1, and Caki-2 cancer cell lines . PBMCs: Peripheral Blood Mononuclear Cells, which are the control cells.
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    Image Search Results


    pH-responsive blocking and restoration of IL-2 receptor binding by UPS 5.3 (A) Schematic of the experimental design to assess the intrinsic interaction between UPS 5.3 micelles and proteins. (B) FPLC chromatograms showing individual proteins or UPS 5.3 /protein mixtures. (C) Molecular docking model of the DBA dimer (blue) with IL-2, highlighting predicted interaction sites. (D–F) Biolayer interferometry analysis of IL-2-Fc binding to IL-2Rα, IL-2Rβ, and IL-2Rγ, with and without UPS 5.3 NP encapsulation. (G) Schematic illustrating ex vivo assessment of IL-2-Fc binding to immune cells from various organs. (H) Quantification of IL-2-Fc binding to lymphocytes isolated from liver, lung, spleen, and tumor ( n = 5). Data are presented as mean ± SEM. See also and .

    Journal: Cell Reports Medicine

    Article Title: Targeting severe acidity for tumor-activatable Interleukin-2 therapy

    doi: 10.1016/j.xcrm.2025.102572

    Figure Lengend Snippet: pH-responsive blocking and restoration of IL-2 receptor binding by UPS 5.3 (A) Schematic of the experimental design to assess the intrinsic interaction between UPS 5.3 micelles and proteins. (B) FPLC chromatograms showing individual proteins or UPS 5.3 /protein mixtures. (C) Molecular docking model of the DBA dimer (blue) with IL-2, highlighting predicted interaction sites. (D–F) Biolayer interferometry analysis of IL-2-Fc binding to IL-2Rα, IL-2Rβ, and IL-2Rγ, with and without UPS 5.3 NP encapsulation. (G) Schematic illustrating ex vivo assessment of IL-2-Fc binding to immune cells from various organs. (H) Quantification of IL-2-Fc binding to lymphocytes isolated from liver, lung, spleen, and tumor ( n = 5). Data are presented as mean ± SEM. See also and .

    Article Snippet: InVivoMAb anti-mouse CD122 (IL-2Rβ) , BioXcell , Cat# BE0298 RRID: AB_2687820.

    Techniques: Blocking Assay, Binding Assay, Encapsulation, Ex Vivo, Isolation

    Expression of IL-2Rα, IL-2Rβ, and IL-2Rγ subunits in renal cell carcinoma cells, demonstrated by PCR products on an agarose gel. Representative blot with relative quantification shows IL-2Rα, IL-2Rβ, and IL-2Rγ protein detection in A-498, ACHN, Caki-1, and Caki-2 cancer cell lines . PBMCs: Peripheral Blood Mononuclear Cells, which are the control cells.

    Journal: Current Issues in Molecular Biology

    Article Title: IL-2 Receptor Expression in Renal Cell Carcinoma Cells: IL-2 Influences Cell Survival and Induces Cell Death

    doi: 10.3390/cimb47100830

    Figure Lengend Snippet: Expression of IL-2Rα, IL-2Rβ, and IL-2Rγ subunits in renal cell carcinoma cells, demonstrated by PCR products on an agarose gel. Representative blot with relative quantification shows IL-2Rα, IL-2Rβ, and IL-2Rγ protein detection in A-498, ACHN, Caki-1, and Caki-2 cancer cell lines . PBMCs: Peripheral Blood Mononuclear Cells, which are the control cells.

    Article Snippet: IL-2Rβ (C-10): sc-393093 , 1:200 , Santa Cruz Biotechnology, Heidelberg, Germany.

    Techniques: Expressing, Agarose Gel Electrophoresis, Quantitative Proteomics, Control

    Protein expression of IL-2Rα, IL-2Rβ, and IL-2Rγ subunits in renal cell carcinoma cells, visualized by Western blot analysis. Representative blot shows IL-2Rα , IL-2Rβ , and IL-2Rγ protein detection in A-498, ACHN, Caki-1, and Caki-2 cancer cell lines. Jurkat cells are the control cells.

    Journal: Current Issues in Molecular Biology

    Article Title: IL-2 Receptor Expression in Renal Cell Carcinoma Cells: IL-2 Influences Cell Survival and Induces Cell Death

    doi: 10.3390/cimb47100830

    Figure Lengend Snippet: Protein expression of IL-2Rα, IL-2Rβ, and IL-2Rγ subunits in renal cell carcinoma cells, visualized by Western blot analysis. Representative blot shows IL-2Rα , IL-2Rβ , and IL-2Rγ protein detection in A-498, ACHN, Caki-1, and Caki-2 cancer cell lines. Jurkat cells are the control cells.

    Article Snippet: IL-2Rβ (C-10): sc-393093 , 1:200 , Santa Cruz Biotechnology, Heidelberg, Germany.

    Techniques: Expressing, Western Blot, Control

    Representative flow cytometry histograms of the IL-2Rγ and IL-2Rβ surface expression for the four RCC cell lines tested. Graphs ( A – D ) show IL-2Rγ expression, and graphs ( E – H ) show IL-2Rβ expression (dark blue curves) with isotype controls (red curves) and unstaining controls (gray curves) in A-498, ACHN, Caki-1, and Caki-2 cell lines.

    Journal: Current Issues in Molecular Biology

    Article Title: IL-2 Receptor Expression in Renal Cell Carcinoma Cells: IL-2 Influences Cell Survival and Induces Cell Death

    doi: 10.3390/cimb47100830

    Figure Lengend Snippet: Representative flow cytometry histograms of the IL-2Rγ and IL-2Rβ surface expression for the four RCC cell lines tested. Graphs ( A – D ) show IL-2Rγ expression, and graphs ( E – H ) show IL-2Rβ expression (dark blue curves) with isotype controls (red curves) and unstaining controls (gray curves) in A-498, ACHN, Caki-1, and Caki-2 cell lines.

    Article Snippet: IL-2Rβ (C-10): sc-393093 , 1:200 , Santa Cruz Biotechnology, Heidelberg, Germany.

    Techniques: Flow Cytometry, Expressing