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goat anti human cd25 polyclonal antibody  (R&D Systems)


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    Structured Review

    R&D Systems goat anti human cd25 polyclonal antibody
    Goat Anti Human Cd25 Polyclonal Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat anti human cd25 polyclonal antibody/product/R&D Systems
    Average 93 stars, based on 9 article reviews
    goat anti human cd25 polyclonal antibody - by Bioz Stars, 2026-04
    93/100 stars

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    R&D Systems polyclonal goat anti human cd25
    Multiple allogeneic mesenchymal stem cell (MSC) injections result in changes in splenic regulatory T cell percentages. (A-D) There were no significant changes in splenic CD21 + B-cell (A) , CD4 + T-cell (B) , or CD8 + T-cell percentages (C) or CD4/CD8 ratios (D) following multiple MSC injections. (E) There were no significant changes in activated <t>(CD25</t> + ) lymphocyte proportions. (F) There were significantly higher percentages of splenic FoxP3 + regulatory T cells in the horses injected with bone marrow (BM)-derived MSCs compared with horses injected with adipose tissue (AT)-derived MSCs. Data are presented as mean ± standard error of the mean. * P <0.05.
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    R&D Systems polyclonal goat anti human il 2ra antibody
    Figure 4. Model of the IL-2R binding to IL-2. Magenta, IL2; yellow, contact site of <t>IL-2Ra</t> and IL-2; red, basiliximab epitope. E116 and V122 mark the first and the last amino acid of the epitope. Orange, overlap of IL-2 binding and basiliximab binding amino acids within the IL-2R. The model was established using the software Cn3D 4.1 based on the published crystal structure (6).
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    Multiple allogeneic mesenchymal stem cell (MSC) injections result in changes in splenic regulatory T cell percentages. (A-D) There were no significant changes in splenic CD21 + B-cell (A) , CD4 + T-cell (B) , or CD8 + T-cell percentages (C) or CD4/CD8 ratios (D) following multiple MSC injections. (E) There were no significant changes in activated (CD25 + ) lymphocyte proportions. (F) There were significantly higher percentages of splenic FoxP3 + regulatory T cells in the horses injected with bone marrow (BM)-derived MSCs compared with horses injected with adipose tissue (AT)-derived MSCs. Data are presented as mean ± standard error of the mean. * P <0.05.

    Journal: Stem Cell Research & Therapy

    Article Title: Multiple intravenous injections of allogeneic equine mesenchymal stem cells do not induce a systemic inflammatory response but do alter lymphocyte subsets in healthy horses

    doi: 10.1186/s13287-015-0050-0

    Figure Lengend Snippet: Multiple allogeneic mesenchymal stem cell (MSC) injections result in changes in splenic regulatory T cell percentages. (A-D) There were no significant changes in splenic CD21 + B-cell (A) , CD4 + T-cell (B) , or CD8 + T-cell percentages (C) or CD4/CD8 ratios (D) following multiple MSC injections. (E) There were no significant changes in activated (CD25 + ) lymphocyte proportions. (F) There were significantly higher percentages of splenic FoxP3 + regulatory T cells in the horses injected with bone marrow (BM)-derived MSCs compared with horses injected with adipose tissue (AT)-derived MSCs. Data are presented as mean ± standard error of the mean. * P <0.05.

    Article Snippet: The following antibodies were used: mouse-anti-equine CD3 (clone UC F6G 1:250; Jeffery Stott, University of California, Davis, CA, USA) [ ], mouse-anti-human CD21 (clone B-ly4 1:20; BD Pharmingen, San Jose, CA, USA) [ , ], polyclonal goat-anti-human CD25 (clone AF-223; R&D Systems) [ ], rat-anti-mouse/human FoxP3 (clone PCH101; ebioscience, San Diego, CA, USA) [ ], mouse-anti-CD4 (clone HB61A 1:133; VMRD, Pullman, WA, USA) [ ], mouse-anti-equine CD8 (clone F18P 1:500; J. Stott) [ ], and a donkey-anti-mouse secondary when necessary (1:50; Jackson ImmunoResearch Laboratories, Inc., West Grove, PA, USA).

    Techniques: Injection, Derivative Assay

    Figure 4. Model of the IL-2R binding to IL-2. Magenta, IL2; yellow, contact site of IL-2Ra and IL-2; red, basiliximab epitope. E116 and V122 mark the first and the last amino acid of the epitope. Orange, overlap of IL-2 binding and basiliximab binding amino acids within the IL-2R. The model was established using the software Cn3D 4.1 based on the published crystal structure (6).

    Journal: Cancer Research

    Article Title: Identification of Their Epitope Reveals the Structural Basis for the Mechanism of Action of the Immunosuppressive Antibodies Basiliximab and Daclizumab

    doi: 10.1158/0008-5472.can-06-3919

    Figure Lengend Snippet: Figure 4. Model of the IL-2R binding to IL-2. Magenta, IL2; yellow, contact site of IL-2Ra and IL-2; red, basiliximab epitope. E116 and V122 mark the first and the last amino acid of the epitope. Orange, overlap of IL-2 binding and basiliximab binding amino acids within the IL-2R. The model was established using the software Cn3D 4.1 based on the published crystal structure (6).

    Article Snippet: After 24 h, cells were stained using basiliximab at 10 Ag/mL or a polyclonal goat anti-human IL-2Ra antibody (R&D Systems) at 7 Ag/mL for 30 min.

    Techniques: Binding Assay, Software