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apc anti mouse ly6c  (Miltenyi Biotec)


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    Structured Review

    Miltenyi Biotec apc anti mouse ly6c
    Apc Anti Mouse Ly6c, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 100 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ly6c+apc+antibodies/Ly-6C+Antibody%2C+anti-mouse%2C+REAfinity/pmc13006431-68-0-6
    Average 95 stars, based on 100 article reviews
    apc anti mouse ly6c - by Bioz Stars, 2026-10
    95/100 stars

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    Related Articles

    other:

    Article Title: Plasmalogen remodeling modulates macrophage response to cytotoxic oxysterols and atherosclerotic plaque vulnerability.
    Article Snippet: Cells were immunostained with CD45-Viogreen, CD115-PE, Ly6C-APC antibodies according to manufacturer’s instructions (Milenyi Biotec).

    Article Title: Plasmalogen remodeling modulates macrophage response to cytotoxic oxysterols and atherosclerotic plaque vulnerability
    Article Snippet: Cells were then resuspended in PBS w/o Ca 2+ -Mg 2+ containing FcR blocking reagent according to manufacturer’s instructions (Miltenyi).



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    The identification of the source of IL-27. (A–D) The intracellular co-label staining by flow cytometry was applied to determine the source of IL-27. The four APCs were labeled by dendritic cell (CD11b, CD11c, B), neutrophil (CD11b, Ly6G, C), monocyte (CD11b, <t>Ly6C,</t> A), and macrophage (CD11b, F4/80, D), respectively. IL-27p28 antibody labeled the IL-27. The results indicated that neutrophil/monocyte-derived IL-27 was highly expressed in serum and spleen. IL: interleukin, APCs: antigen-presenting cells, SSC-A: side scatter area.
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    The identification of the source of IL-27. (A–D) The intracellular co-label staining by flow cytometry was applied to determine the source of IL-27. The four APCs were labeled by dendritic cell (CD11b, CD11c, B), neutrophil (CD11b, Ly6G, C), monocyte (CD11b, <t>Ly6C,</t> A), and macrophage (CD11b, F4/80, D), respectively. IL-27p28 antibody labeled the IL-27. The results indicated that neutrophil/monocyte-derived IL-27 was highly expressed in serum and spleen. IL: interleukin, APCs: antigen-presenting cells, SSC-A: side scatter area.
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    The identification of the source of IL-27. (A–D) The intracellular co-label staining by flow cytometry was applied to determine the source of IL-27. The four APCs were labeled by dendritic cell (CD11b, CD11c, B), neutrophil (CD11b, Ly6G, C), monocyte (CD11b, Ly6C, A), and macrophage (CD11b, F4/80, D), respectively. IL-27p28 antibody labeled the IL-27. The results indicated that neutrophil/monocyte-derived IL-27 was highly expressed in serum and spleen. IL: interleukin, APCs: antigen-presenting cells, SSC-A: side scatter area.

    Journal: The Korean Journal of Pain

    Article Title: IL-27-Ucp2-FoxO3 axis mediating the polarization of alternatively activated macrophages and ameliorating inflammatory pain

    doi: 10.3344/kjp.25307

    Figure Lengend Snippet: The identification of the source of IL-27. (A–D) The intracellular co-label staining by flow cytometry was applied to determine the source of IL-27. The four APCs were labeled by dendritic cell (CD11b, CD11c, B), neutrophil (CD11b, Ly6G, C), monocyte (CD11b, Ly6C, A), and macrophage (CD11b, F4/80, D), respectively. IL-27p28 antibody labeled the IL-27. The results indicated that neutrophil/monocyte-derived IL-27 was highly expressed in serum and spleen. IL: interleukin, APCs: antigen-presenting cells, SSC-A: side scatter area.

    Article Snippet: APC Anti-Mouse Ly6C , Elabscience , E-AB-F1121E.

    Techniques: Staining, Flow Cytometry, Labeling, Derivative Assay