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soluble il 6rα  (R&D Systems)


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    Structured Review

    R&D Systems soluble il 6rα
    Soluble Il 6rα, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 82 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/soluble il 6rα/product/R&D Systems
    Average 95 stars, based on 82 article reviews
    soluble il 6rα - by Bioz Stars, 2026-02
    95/100 stars

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    R&D Systems soluble il‐6 receptor alpha (il‐6rα) enzyme-linked immunosorbent assay (elisa) kits
    (A‐D) MaR1 reduced Aβ 42 ‐induced secretion of pro‐inflammatory cytokines in d‐THP‐1 cells. Differentiated THP‐1 (d‐THP‐1) cells were incubated with vehicle, 5 µM Aβ 42 , 5 µmol/L MaR1 or 5 µM Aβ 42 + 5 µM MaR1 for 24 h and the supernatants were analysed by ELISA. A total of 14 experiments were performed. MaR1 reduced the Aβ 42 ‐induced increase in interleukin (IL)‐1β (A), tumour necrosis factor (TNF)‐α (B) <t>and</t> <t>IL‐6</t> (C). The levels of IL‐6 receptor (R) α (D) were not affected by Aβ 42 nor MaR1. Analysis of variance (ANOVA) was performed with the non‐parametric Kruskal–Wallis (K‐W) test, using the built‐in post hoc test for multiple comparisons to find significant differences between treatments. *** P < 0.005 vs. vehicle. # P < 0.05, ## P < 0.01, ### P < 0.005 vs. 5 μM Aβ 42 . Aβ = β‐amyloid; MaR1 = maresin 1
    Soluble Il‐6 Receptor Alpha (Il‐6rα) Enzyme Linked Immunosorbent Assay (Elisa) Kits, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 90 stars, based on 1 article reviews
    soluble il‐6 receptor alpha (il‐6rα) enzyme-linked immunosorbent assay (elisa) kits - by Bioz Stars, 2026-02
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    (A‐D) MaR1 reduced Aβ 42 ‐induced secretion of pro‐inflammatory cytokines in d‐THP‐1 cells. Differentiated THP‐1 (d‐THP‐1) cells were incubated with vehicle, 5 µM Aβ 42 , 5 µmol/L MaR1 or 5 µM Aβ 42 + 5 µM MaR1 for 24 h and the supernatants were analysed by ELISA. A total of 14 experiments were performed. MaR1 reduced the Aβ 42 ‐induced increase in interleukin (IL)‐1β (A), tumour necrosis factor (TNF)‐α (B) and IL‐6 (C). The levels of IL‐6 receptor (R) α (D) were not affected by Aβ 42 nor MaR1. Analysis of variance (ANOVA) was performed with the non‐parametric Kruskal–Wallis (K‐W) test, using the built‐in post hoc test for multiple comparisons to find significant differences between treatments. *** P < 0.005 vs. vehicle. # P < 0.05, ## P < 0.01, ### P < 0.005 vs. 5 μM Aβ 42 . Aβ = β‐amyloid; MaR1 = maresin 1

    Journal: Journal of Cellular and Molecular Medicine

    Article Title: Maresin 1 attenuates pro‐inflammatory activation induced by β‐amyloid and stimulates its uptake

    doi: 10.1111/jcmm.16098

    Figure Lengend Snippet: (A‐D) MaR1 reduced Aβ 42 ‐induced secretion of pro‐inflammatory cytokines in d‐THP‐1 cells. Differentiated THP‐1 (d‐THP‐1) cells were incubated with vehicle, 5 µM Aβ 42 , 5 µmol/L MaR1 or 5 µM Aβ 42 + 5 µM MaR1 for 24 h and the supernatants were analysed by ELISA. A total of 14 experiments were performed. MaR1 reduced the Aβ 42 ‐induced increase in interleukin (IL)‐1β (A), tumour necrosis factor (TNF)‐α (B) and IL‐6 (C). The levels of IL‐6 receptor (R) α (D) were not affected by Aβ 42 nor MaR1. Analysis of variance (ANOVA) was performed with the non‐parametric Kruskal–Wallis (K‐W) test, using the built‐in post hoc test for multiple comparisons to find significant differences between treatments. *** P < 0.005 vs. vehicle. # P < 0.05, ## P < 0.01, ### P < 0.005 vs. 5 μM Aβ 42 . Aβ = β‐amyloid; MaR1 = maresin 1

    Article Snippet: Human tumour necrosis factor (TNF)‐α, IL‐1β, IL‐6, soluble IL‐6 receptor alpha (IL‐6Rα) and IL‐1 receptor type II enzyme‐linked immunosorbent assay (ELISA) kits and recombinant human monocyte chemoattractant protein (MCP)‐1 protein were purchased from R&D Systems (Abingdon, United Kingdom).

    Techniques: Incubation, Enzyme-linked Immunosorbent Assay

    (A‐C) MaR1 reduced Aβ 42 ‐induced pro‐inflammatory cytokine secretion in human MdM. Human monocyte‐derived microglia (MdM) were incubated with vehicle, 5 µM Aβ 42 , 5 µM MaR1 or 5 µM Aβ 42 + 5 µM MaR1 for 24 h. The levels of interleukin (IL)‐1β (A), tumour necrosis factor (TNF)‐α (B) and IL‐6 (C) were determined in the cell supernatants using a V‐PLEX human pro‐inflammatory panel. A total of 5 experiments were performed. Aβ 42 increased the levels of IL‐1β (A), TNF‐α (B) and IL‐6 (C), while co‐incubation with MaR1 reduced the elevation (A‐C). Analysis of variance (ANOVA) was performed with the Kruskal–Wallis (K‐W) test followed by pair‐wise comparisons of groups using Mann‐Withney with Bonferroni correction for multiple comparisons. * P < 0.05 vs. vehicle. # P < 0.05 vs. 5 μM Aβ 42 . Aβ = β‐amyloid; MaR1 = maresin 1

    Journal: Journal of Cellular and Molecular Medicine

    Article Title: Maresin 1 attenuates pro‐inflammatory activation induced by β‐amyloid and stimulates its uptake

    doi: 10.1111/jcmm.16098

    Figure Lengend Snippet: (A‐C) MaR1 reduced Aβ 42 ‐induced pro‐inflammatory cytokine secretion in human MdM. Human monocyte‐derived microglia (MdM) were incubated with vehicle, 5 µM Aβ 42 , 5 µM MaR1 or 5 µM Aβ 42 + 5 µM MaR1 for 24 h. The levels of interleukin (IL)‐1β (A), tumour necrosis factor (TNF)‐α (B) and IL‐6 (C) were determined in the cell supernatants using a V‐PLEX human pro‐inflammatory panel. A total of 5 experiments were performed. Aβ 42 increased the levels of IL‐1β (A), TNF‐α (B) and IL‐6 (C), while co‐incubation with MaR1 reduced the elevation (A‐C). Analysis of variance (ANOVA) was performed with the Kruskal–Wallis (K‐W) test followed by pair‐wise comparisons of groups using Mann‐Withney with Bonferroni correction for multiple comparisons. * P < 0.05 vs. vehicle. # P < 0.05 vs. 5 μM Aβ 42 . Aβ = β‐amyloid; MaR1 = maresin 1

    Article Snippet: Human tumour necrosis factor (TNF)‐α, IL‐1β, IL‐6, soluble IL‐6 receptor alpha (IL‐6Rα) and IL‐1 receptor type II enzyme‐linked immunosorbent assay (ELISA) kits and recombinant human monocyte chemoattractant protein (MCP)‐1 protein were purchased from R&D Systems (Abingdon, United Kingdom).

    Techniques: Derivative Assay, Incubation