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milliplex maptm 32-mouse-plex cytokine detection system  (Millipore)

 
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    Structured Review

    Millipore milliplex maptm 32-mouse-plex cytokine detection system
    Milliplex Maptm 32 Mouse Plex Cytokine Detection System, supplied by Millipore, 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/milliplex maptm 32-mouse-plex cytokine detection system/product/Millipore
    Average 90 stars, based on 1 article reviews
    milliplex maptm 32-mouse-plex cytokine detection system - by Bioz Stars, 2026-03
    90/100 stars

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    Naringenin downregulates inflammatory mediators in C. trachomatis infected mouse J774 macrophages. Macrophages (10 6 cells/mL) were seeded in 24-well plates and were either infected with live C. trachomatis (10 5 IFU/well) or LPS at 1 μ g/mL. After 2-day infection, naringenin at 0.01 to 10 μ g/mL was added to cell cultures and the production levels of cytokines (a) and <t>chemokines</t> (b) were quantified in supernatants collected 2 days later employing multiplex ELISA. ***indicates significant difference ( P < 0.001) between C. trachomatis treated cells and those treated with various concentrations of naringenin using the two-tailed unpaired Student's t -test. Each bar represents the average of samples run in duplicates and the data are representative of three separate experiments.
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    Average 90 stars, based on 1 article reviews
    milliplex map tm 32-mouse plex cytokine detection system - by Bioz Stars, 2026-03
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    90
    Millipore milliplex mouse 32-plex cytokine and chemokine detection system
    BMDM were stimulated with live Bb or L-OspA in the presence or absence of exogenous or α-IL-10 (or its isotype control) Ab as described in and . Cell-free supernatants were harvested from cultures at 24 h and protein determinations were made by multiplex ELISA. Fold decrease (A) was calculated as stimulant/stimulant exposed to exogenous IL-10. Fold increase (B) was calculated as stimulant + α IL-10 Ab/stimulant+isotype control Ab. A one-way ANOVA followed by a Bonferroni post-hoc test in conjugation with two tailed Mann Whitney test was used for data analyses. Significance was established at P <0.001 = ***, P <0.01 = ** and P <0.05 = *. Each symbol represents fold change for a specific cytokine or <t>chemokine.</t> Each fold change is representative of two independent experiments.
    Milliplex Mouse 32 Plex Cytokine And Chemokine Detection System, supplied by Millipore, 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/milliplex mouse 32-plex cytokine and chemokine detection system/product/Millipore
    Average 90 stars, based on 1 article reviews
    milliplex mouse 32-plex cytokine and chemokine detection system - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

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    Naringenin downregulates inflammatory mediators in C. trachomatis infected mouse J774 macrophages. Macrophages (10 6 cells/mL) were seeded in 24-well plates and were either infected with live C. trachomatis (10 5 IFU/well) or LPS at 1 μ g/mL. After 2-day infection, naringenin at 0.01 to 10 μ g/mL was added to cell cultures and the production levels of cytokines (a) and chemokines (b) were quantified in supernatants collected 2 days later employing multiplex ELISA. ***indicates significant difference ( P < 0.001) between C. trachomatis treated cells and those treated with various concentrations of naringenin using the two-tailed unpaired Student's t -test. Each bar represents the average of samples run in duplicates and the data are representative of three separate experiments.

    Journal: Mediators of Inflammation

    Article Title: Flavonoid Naringenin: A Potential Immunomodulator for Chlamydia trachomatis Inflammation

    doi: 10.1155/2013/102457

    Figure Lengend Snippet: Naringenin downregulates inflammatory mediators in C. trachomatis infected mouse J774 macrophages. Macrophages (10 6 cells/mL) were seeded in 24-well plates and were either infected with live C. trachomatis (10 5 IFU/well) or LPS at 1 μ g/mL. After 2-day infection, naringenin at 0.01 to 10 μ g/mL was added to cell cultures and the production levels of cytokines (a) and chemokines (b) were quantified in supernatants collected 2 days later employing multiplex ELISA. ***indicates significant difference ( P < 0.001) between C. trachomatis treated cells and those treated with various concentrations of naringenin using the two-tailed unpaired Student's t -test. Each bar represents the average of samples run in duplicates and the data are representative of three separate experiments.

    Article Snippet: Milliplex mouse 32-plex cytokine and chemokines detection reagent (catalogue number MPXMCYTO-70 K-PMX32) was purchased from Millipore (EMD Millipore Corporation, Billerica, MA, USA) and the assay was performed as described [ ].

    Techniques: Infection, Multiplex Assay, Enzyme-linked Immunosorbent Assay, Two Tailed Test

    BMDM were stimulated with live Bb or L-OspA in the presence or absence of exogenous or α-IL-10 (or its isotype control) Ab as described in and . Cell-free supernatants were harvested from cultures at 24 h and protein determinations were made by multiplex ELISA. Fold decrease (A) was calculated as stimulant/stimulant exposed to exogenous IL-10. Fold increase (B) was calculated as stimulant + α IL-10 Ab/stimulant+isotype control Ab. A one-way ANOVA followed by a Bonferroni post-hoc test in conjugation with two tailed Mann Whitney test was used for data analyses. Significance was established at P <0.001 = ***, P <0.01 = ** and P <0.05 = *. Each symbol represents fold change for a specific cytokine or chemokine. Each fold change is representative of two independent experiments.

    Journal: PLoS ONE

    Article Title: Different Patterns of Expression and of IL-10 Modulation of Inflammatory Mediators from Macrophages of Lyme Disease-Resistant and -Susceptible Mice

    doi: 10.1371/journal.pone.0043860

    Figure Lengend Snippet: BMDM were stimulated with live Bb or L-OspA in the presence or absence of exogenous or α-IL-10 (or its isotype control) Ab as described in and . Cell-free supernatants were harvested from cultures at 24 h and protein determinations were made by multiplex ELISA. Fold decrease (A) was calculated as stimulant/stimulant exposed to exogenous IL-10. Fold increase (B) was calculated as stimulant + α IL-10 Ab/stimulant+isotype control Ab. A one-way ANOVA followed by a Bonferroni post-hoc test in conjugation with two tailed Mann Whitney test was used for data analyses. Significance was established at P <0.001 = ***, P <0.01 = ** and P <0.05 = *. Each symbol represents fold change for a specific cytokine or chemokine. Each fold change is representative of two independent experiments.

    Article Snippet: Concentrations of inflammatory mediators were quantified in cell-free supernatants of BMDM cultures using the Milliplex mouse 32-plex cytokine and chemokine detection system (Millipore Corporation, Bedford, MA) according to the manufacturer's instructions.

    Techniques: Control, Multiplex Assay, Enzyme-linked Immunosorbent Assay, Conjugation Assay, Two Tailed Test, MANN-WHITNEY