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cd40 pe vio 770 clone rea965  (Miltenyi Biotec)


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    Miltenyi Biotec cd40 pe vio 770 clone rea965
    Cd40 Pe Vio 770 Clone Rea965, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 93/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cd40 pe vio 770 clone rea965/product/Miltenyi Biotec
    Average 93 stars, based on 10 article reviews
    cd40 pe vio 770 clone rea965 - by Bioz Stars, 2026-03
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    Cd40 Pe Vio 770 Clone Rea965, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    SULF A-dependent modulation of microglial activation and arginine metabolism. ( A ) RT-PCR analysis of cytokine and microglial marker gene expression following 24 h treatment. ( B ) CCL2 secretion quantified by ELISA at 48 h (n = 12). ( C ) Flow cytometric analysis of surface marker expression (CD40, CD86, MHC II, CD200R, TREM2) on untreated microglia (CTRL) or cells treated with 10 µg/mL SULF A for 24 h, expressed as mean fluorescence intensity (MFI; n = 6). ( D ) Schematic of iNOS/ARG metabolic pathways. ( E ) Quantification of nitric oxide (NO) release in culture supernatants by Griess assay at 48 h (n = 12). ( F ) Frequency of microglial cells expressing ARG, iNOS, or both, after 48 h of SULF A treatment (n = 6); ( G–H ) Representative FACS plots showing ARG⁺, iNOS⁺, and ARG⁺iNOS⁺ populations in untreated and SULF A-treated microglia. Data represent mean ± SEM. Statistical significance determined by paired t-test (P < 0.05; **P < 0.001; ***P < 0.0001)

    Journal: Journal of Neuroinflammation

    Article Title: Microglial clearance, neuroprotection and cognitive recovery via a novel synthetic sulfolipid in Alzheimer’s disease

    doi: 10.1186/s12974-025-03634-w

    Figure Lengend Snippet: SULF A-dependent modulation of microglial activation and arginine metabolism. ( A ) RT-PCR analysis of cytokine and microglial marker gene expression following 24 h treatment. ( B ) CCL2 secretion quantified by ELISA at 48 h (n = 12). ( C ) Flow cytometric analysis of surface marker expression (CD40, CD86, MHC II, CD200R, TREM2) on untreated microglia (CTRL) or cells treated with 10 µg/mL SULF A for 24 h, expressed as mean fluorescence intensity (MFI; n = 6). ( D ) Schematic of iNOS/ARG metabolic pathways. ( E ) Quantification of nitric oxide (NO) release in culture supernatants by Griess assay at 48 h (n = 12). ( F ) Frequency of microglial cells expressing ARG, iNOS, or both, after 48 h of SULF A treatment (n = 6); ( G–H ) Representative FACS plots showing ARG⁺, iNOS⁺, and ARG⁺iNOS⁺ populations in untreated and SULF A-treated microglia. Data represent mean ± SEM. Statistical significance determined by paired t-test (P < 0.05; **P < 0.001; ***P < 0.0001)

    Article Snippet: Surface markers were assessed by staining with anti-mouse CD11b-VioBlue, CD40-PE, CD86-FITC, CD200R-APC (Miltenyi Biotec), and TREM2-APC (R&D Systems) according to standard protocols.

    Techniques: Activation Assay, Reverse Transcription Polymerase Chain Reaction, Marker, Gene Expression, Enzyme-linked Immunosorbent Assay, Expressing, Fluorescence, Griess Assay