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primary antibodies against cd86 nbp2-25208  (Novus Biologicals)


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    Novus Biologicals primary antibodies against cd86 nbp2-25208
    Effect of CEMMS on the polarization of rat macrophages. A) Quantitative analysis of M1 macrophage-related phenotypes using real-time PCR (n = 3). B) Quantitative analysis of M2 macrophage-related phenotypes using real-time PCR (n = 3). C) Immunofluorescence staining for markers of <t>macrophages(CD86;</t> Green)/(CD206; Red). Scale bars: 100 μm. D) Quantitative analysis of immunofuorescence staining. E) Immunofluorescence staining for markers of macrophages (Arg-1; Green)/(IL-1β; Red). Scale bars: 100 μm. F) Quantitative analysis of immunofuorescence staining. ∗∗∗∗ p < 0.0001.
    Primary Antibodies Against Cd86 Nbp2 25208, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary antibodies against cd86 nbp2-25208/product/Novus Biologicals
    Average 90 stars, based on 1 article reviews
    primary antibodies against cd86 nbp2-25208 - by Bioz Stars, 2026-03
    90/100 stars

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    1) Product Images from "Construction of cartilaginous organoids based on cartilage extracellular matrix microcarriers to promote articular cartilage regeneration through immune regulation"

    Article Title: Construction of cartilaginous organoids based on cartilage extracellular matrix microcarriers to promote articular cartilage regeneration through immune regulation

    Journal: Journal of Orthopaedic Translation

    doi: 10.1016/j.jot.2025.05.005

    Effect of CEMMS on the polarization of rat macrophages. A) Quantitative analysis of M1 macrophage-related phenotypes using real-time PCR (n = 3). B) Quantitative analysis of M2 macrophage-related phenotypes using real-time PCR (n = 3). C) Immunofluorescence staining for markers of macrophages(CD86; Green)/(CD206; Red). Scale bars: 100 μm. D) Quantitative analysis of immunofuorescence staining. E) Immunofluorescence staining for markers of macrophages (Arg-1; Green)/(IL-1β; Red). Scale bars: 100 μm. F) Quantitative analysis of immunofuorescence staining. ∗∗∗∗ p < 0.0001.
    Figure Legend Snippet: Effect of CEMMS on the polarization of rat macrophages. A) Quantitative analysis of M1 macrophage-related phenotypes using real-time PCR (n = 3). B) Quantitative analysis of M2 macrophage-related phenotypes using real-time PCR (n = 3). C) Immunofluorescence staining for markers of macrophages(CD86; Green)/(CD206; Red). Scale bars: 100 μm. D) Quantitative analysis of immunofuorescence staining. E) Immunofluorescence staining for markers of macrophages (Arg-1; Green)/(IL-1β; Red). Scale bars: 100 μm. F) Quantitative analysis of immunofuorescence staining. ∗∗∗∗ p < 0.0001.

    Techniques Used: Real-time Polymerase Chain Reaction, Immunofluorescence, Staining



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    Image Search Results


    Effect of CEMMS on the polarization of rat macrophages. A) Quantitative analysis of M1 macrophage-related phenotypes using real-time PCR (n = 3). B) Quantitative analysis of M2 macrophage-related phenotypes using real-time PCR (n = 3). C) Immunofluorescence staining for markers of macrophages(CD86; Green)/(CD206; Red). Scale bars: 100 μm. D) Quantitative analysis of immunofuorescence staining. E) Immunofluorescence staining for markers of macrophages (Arg-1; Green)/(IL-1β; Red). Scale bars: 100 μm. F) Quantitative analysis of immunofuorescence staining. ∗∗∗∗ p < 0.0001.

    Journal: Journal of Orthopaedic Translation

    Article Title: Construction of cartilaginous organoids based on cartilage extracellular matrix microcarriers to promote articular cartilage regeneration through immune regulation

    doi: 10.1016/j.jot.2025.05.005

    Figure Lengend Snippet: Effect of CEMMS on the polarization of rat macrophages. A) Quantitative analysis of M1 macrophage-related phenotypes using real-time PCR (n = 3). B) Quantitative analysis of M2 macrophage-related phenotypes using real-time PCR (n = 3). C) Immunofluorescence staining for markers of macrophages(CD86; Green)/(CD206; Red). Scale bars: 100 μm. D) Quantitative analysis of immunofuorescence staining. E) Immunofluorescence staining for markers of macrophages (Arg-1; Green)/(IL-1β; Red). Scale bars: 100 μm. F) Quantitative analysis of immunofuorescence staining. ∗∗∗∗ p < 0.0001.

    Article Snippet: The cells were incubated with primary antibodies against CD86 (NBP2-25208, Novus), CD206 (24595S, CST), IL-1β(ab254360, Abcam) and Arg-1 (66129-1-Ig, proteintech) overnight at 4 °C.

    Techniques: Real-time Polymerase Chain Reaction, Immunofluorescence, Staining