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pe anti human cd206 mmr  (Miltenyi Biotec)


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    Miltenyi Biotec pe anti human cd206 mmr
    Pe Anti Human Cd206 Mmr, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 40 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/pe anti human cd206 mmr/product/Miltenyi Biotec
    Average 95 stars, based on 40 article reviews
    pe anti human cd206 mmr - by Bioz Stars, 2026-03
    95/100 stars

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    SP@CSC alleviate IBD Inducing Factors in Macrophages. Cytoprotective effect of different treatments against H 2 O 2 -induced oxidative stress in RAW264.7 cells (a) and HT-29 cells (b). (c) Flow cytometry analysis of DCFH-DA staining in LPS-induced (1 μg/mL) RAW264.7 cells under various treatment conditions, along with (d) the corresponding quantitative evaluation. (e) Flow cytometry analysis of the proportions of CD86-positive and CD206-positive macrophages after LPS stimulation for 24 h. (f) Quantification of CD86-positive and CD206-negative cells across all groups. ELISA assays of typical proinflammatory of TNF-α (g), IL-6 (h). (i) Western blot assay for Nrf2, and HO-1expression of Raw 264.7 cells after LPS stimulation and treated with different treatments. Data are presented as mean ± S.D (n = 3 per group). Statistical significance was assessed using one-way ANOVA test. ∗ P < 0.05, ∗∗ P < 0.01.

    Journal: Materials Today Bio

    Article Title: Microalgal-enhanced cerium oxide nanotherapeutics for alleviating inflammatory bowel disease via scavenging reactive oxygen species and modulating gut microbiota in colitis

    doi: 10.1016/j.mtbio.2025.101945

    Figure Lengend Snippet: SP@CSC alleviate IBD Inducing Factors in Macrophages. Cytoprotective effect of different treatments against H 2 O 2 -induced oxidative stress in RAW264.7 cells (a) and HT-29 cells (b). (c) Flow cytometry analysis of DCFH-DA staining in LPS-induced (1 μg/mL) RAW264.7 cells under various treatment conditions, along with (d) the corresponding quantitative evaluation. (e) Flow cytometry analysis of the proportions of CD86-positive and CD206-positive macrophages after LPS stimulation for 24 h. (f) Quantification of CD86-positive and CD206-negative cells across all groups. ELISA assays of typical proinflammatory of TNF-α (g), IL-6 (h). (i) Western blot assay for Nrf2, and HO-1expression of Raw 264.7 cells after LPS stimulation and treated with different treatments. Data are presented as mean ± S.D (n = 3 per group). Statistical significance was assessed using one-way ANOVA test. ∗ P < 0.05, ∗∗ P < 0.01.

    Article Snippet: Antibodies for flow cytometry, specifically CD206-PE and CD86-FITC, along with ELISA kits for catalase (CAT), superoxide dismutase (SOD), interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), and interleukin-17 (IL-17), were purchased from Elabscience Biotechnology Co., Ltd. (Wuhan, China).

    Techniques: Flow Cytometry, Staining, Enzyme-linked Immunosorbent Assay, Western Blot