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pe conjugated anti human ido  (R&D Systems)


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    R&D Systems pe conjugated anti human ido
    Pe Conjugated Anti Human Ido, supplied by R&D Systems, used in various techniques. Bioz Stars score: 91/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pe+conjugated+anti+human+ido/us12589163-1108-0-4?v=R%26D+Systems
    Average 91 stars, based on 9 article reviews
    pe conjugated anti human ido - by Bioz Stars, 2026-07
    91/100 stars

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    FIGURE 1. Phenotypic and functional characteristics of human umbilical cord blood-derived MDSCs. (A) Flow cytometry was used to analyze MDSCs stained with individual MDSC surface marker antibodies. (B) The expression of immune suppressive molecules in MDSCs, as indicated by staining <t>with</t> <t>FITC</t> anti-iNOS2 antibody, PE <t>anti-IDO</t> antibody, and PerCP-Cy5.5 anti-ARG1 antibody.
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    Figure 6. Modulation in expression of tumor suppressor proteins and oncogenes in MDA231 cells treated with preconditioned CVMSCs: flow cytometry analysis for the expression of tumor suppressor proteins modulated in MDA231 cells after treatment with preconditioned CVMSCs showed significant increase in the expression levels for CDH1 <t>and</t> <t>IFN-gamma</t> in both IC and CM settings as compared to untreated control (A(i)). Expression levels of oncogenes such as <t>IDO,</t> IL6, MMP7, and TGF-β1 reduced significantly in MDA231 cells in both IC and SF setting as compared to untreated control (B(i)). Data obtained by FACS analysis from three independent experiments were quantified and are shown in bar graphs as Mean Florescence Index (MFI) pertaining to CDH1 and IFN-gamma (A(ii)), and IDO, IL6, MMP7, and TGF-β1 (B(ii)), respectively. Bars represent standard errors. * p < 0.05.
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    FIGURE 1. Phenotypic and functional characteristics of human umbilical cord blood-derived MDSCs. (A) Flow cytometry was used to analyze MDSCs stained with individual MDSC surface marker antibodies. (B) The expression of immune suppressive molecules in MDSCs, as indicated by staining with FITC anti-iNOS2 antibody, PE anti-IDO antibody, and PerCP-Cy5.5 anti-ARG1 antibody.

    Journal: Investigative ophthalmology & visual science

    Article Title: Local Myeloid-Derived Suppressor Cells Impair Progression of Experimental Autoimmune Uveitis by Alleviating Oxidative Stress and Inflammation.

    doi: 10.1167/iovs.64.13.39

    Figure Lengend Snippet: FIGURE 1. Phenotypic and functional characteristics of human umbilical cord blood-derived MDSCs. (A) Flow cytometry was used to analyze MDSCs stained with individual MDSC surface marker antibodies. (B) The expression of immune suppressive molecules in MDSCs, as indicated by staining with FITC anti-iNOS2 antibody, PE anti-IDO antibody, and PerCP-Cy5.5 anti-ARG1 antibody.

    Article Snippet: For intracellular staining of iNOS FITC (Cat# SC-7271, FITC, Santa Cruz Biotechnology, Dallas, TX, USA), IDO PE (Cat# IC6030P, R&D Systems, Bio-Techne, Minneapolis, MN, USA), and ARG1 PerCP (Cat# IC8026C, R&D Systems).

    Techniques: Functional Assay, Derivative Assay, Flow Cytometry, Staining, Marker, Expressing

    Figure 6. Modulation in expression of tumor suppressor proteins and oncogenes in MDA231 cells treated with preconditioned CVMSCs: flow cytometry analysis for the expression of tumor suppressor proteins modulated in MDA231 cells after treatment with preconditioned CVMSCs showed significant increase in the expression levels for CDH1 and IFN-gamma in both IC and CM settings as compared to untreated control (A(i)). Expression levels of oncogenes such as IDO, IL6, MMP7, and TGF-β1 reduced significantly in MDA231 cells in both IC and SF setting as compared to untreated control (B(i)). Data obtained by FACS analysis from three independent experiments were quantified and are shown in bar graphs as Mean Florescence Index (MFI) pertaining to CDH1 and IFN-gamma (A(ii)), and IDO, IL6, MMP7, and TGF-β1 (B(ii)), respectively. Bars represent standard errors. * p < 0.05.

    Journal: International journal of molecular sciences

    Article Title: Preconditioned Chorionic Villus Mesenchymal Stem/Stromal Cells (CVMSCs) Minimize the Invasive Phenotypes of Breast Cancer Cell Line MDA231 In Vitro.

    doi: 10.3390/ijms24119569

    Figure Lengend Snippet: Figure 6. Modulation in expression of tumor suppressor proteins and oncogenes in MDA231 cells treated with preconditioned CVMSCs: flow cytometry analysis for the expression of tumor suppressor proteins modulated in MDA231 cells after treatment with preconditioned CVMSCs showed significant increase in the expression levels for CDH1 and IFN-gamma in both IC and CM settings as compared to untreated control (A(i)). Expression levels of oncogenes such as IDO, IL6, MMP7, and TGF-β1 reduced significantly in MDA231 cells in both IC and SF setting as compared to untreated control (B(i)). Data obtained by FACS analysis from three independent experiments were quantified and are shown in bar graphs as Mean Florescence Index (MFI) pertaining to CDH1 and IFN-gamma (A(ii)), and IDO, IL6, MMP7, and TGF-β1 (B(ii)), respectively. Bars represent standard errors. * p < 0.05.

    Article Snippet: Fluorescent-labeled antibodies for flow cytometry experiments, including IFN-γ (Human IFN-gamma PE-conjugated Antibody) cat# IC285P; CDH1 (Human E-Cadherin PE-conjugated Antibody) cat# FAB18381P; IDO (Human Indoleamine 2,3-dioxygenase/IDO PE-conjugated Antibody) cat# IC6030P; IL6 (Human IL-6 PE-conjugated Antibody)cat# IC206P; MMP7 (Human MMP-7 PE-conjugated Antibody) cat# IC9071P; and TGF-β1 (Human TGF-beta 1 Alexa Fluor® 488-conjugated Antibody) cat# IC10502G were purchased from R&D Systems (Minneapolis, MN, USA).

    Techniques: Expressing, Cytometry, Control