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proteome profiler human cytokine antibody array xl  (R&D Systems)


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    R&D Systems proteome profiler human cytokine antibody array xl
    Proteome Profiler Human Cytokine Antibody Array Xl, supplied by R&D Systems, used in various techniques. Bioz Stars score: 96/100, based on 545 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+proteome+profiler+antibody+array+kits/Proteome+Profiler+Human+Cytokine+Array+Kit/pm41638316-83-12-19
    Average 96 stars, based on 545 article reviews
    proteome profiler human cytokine antibody array xl - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Protein-Protein interactions:

    Article Title: New Plant Extracts Exert Complementary Anti‐Hair Loss Properties in Human In Vitro and Ex Vivo Models
    Article Snippet: .. Growth factor receptor (GFR) signaling pathways were analyzed using two Human Proteome Profiler antibody array kits (R&D Systems, USA) to simultaneously detect the phosphorylation of 49 receptor tyrosine kinases (Proteome Profiler Human Phospho‐RTK Array Kit) and of 43 kinases and two related total proteins (Proteome Profiler Human Phospho‐Kinase Array Kit). ..

    Article Title: New Plant Extracts Exert Complementary Anti-Hair Loss Properties in Human In Vitro and Ex Vivo Models.
    Article Snippet: .. Growth factor receptor (GFR) signaling pathways were analyzed using two Human Proteome Profiler antibody array kits (R&D Systems, USA) to simultaneously detect the phosphorylation of 49 receptor tyrosine kinases (Proteome Profiler Human Phospho- RTK Array Kit) and of 43 kinases and two related total proteins (Proteome Profiler Human PhosphoKinase Array Kit). ..

    Ab Array:

    Article Title: New Plant Extracts Exert Complementary Anti‐Hair Loss Properties in Human In Vitro and Ex Vivo Models
    Article Snippet: .. Growth factor receptor (GFR) signaling pathways were analyzed using two Human Proteome Profiler antibody array kits (R&D Systems, USA) to simultaneously detect the phosphorylation of 49 receptor tyrosine kinases (Proteome Profiler Human Phospho‐RTK Array Kit) and of 43 kinases and two related total proteins (Proteome Profiler Human Phospho‐Kinase Array Kit). ..

    Article Title: New Plant Extracts Exert Complementary Anti-Hair Loss Properties in Human In Vitro and Ex Vivo Models.
    Article Snippet: .. Growth factor receptor (GFR) signaling pathways were analyzed using two Human Proteome Profiler antibody array kits (R&D Systems, USA) to simultaneously detect the phosphorylation of 49 receptor tyrosine kinases (Proteome Profiler Human Phospho- RTK Array Kit) and of 43 kinases and two related total proteins (Proteome Profiler Human PhosphoKinase Array Kit). ..

    Phospho-proteomics:

    Article Title: New Plant Extracts Exert Complementary Anti‐Hair Loss Properties in Human In Vitro and Ex Vivo Models
    Article Snippet: .. Growth factor receptor (GFR) signaling pathways were analyzed using two Human Proteome Profiler antibody array kits (R&D Systems, USA) to simultaneously detect the phosphorylation of 49 receptor tyrosine kinases (Proteome Profiler Human Phospho‐RTK Array Kit) and of 43 kinases and two related total proteins (Proteome Profiler Human Phospho‐Kinase Array Kit). ..

    Article Title: New Plant Extracts Exert Complementary Anti-Hair Loss Properties in Human In Vitro and Ex Vivo Models.
    Article Snippet: .. Growth factor receptor (GFR) signaling pathways were analyzed using two Human Proteome Profiler antibody array kits (R&D Systems, USA) to simultaneously detect the phosphorylation of 49 receptor tyrosine kinases (Proteome Profiler Human Phospho- RTK Array Kit) and of 43 kinases and two related total proteins (Proteome Profiler Human PhosphoKinase Array Kit). ..



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    ( A ) Schematic of molecular mechanisms of COVID-19 and dsRNA induced IFN response. Ruxolitinib suppresses IFN-stimulated response and mitoTEMPO suppresses mitochondrial damage and oxidative stress. (Created with BioRender.com.) ( B and C ) Inhibition of JAK/STAT signaling with ruxolitinib (Rux) (1 μM) significantly suppressed PIC-mediated induction of the interferon response signaling proteins STAT1, p-STAT1, IRF9, and MX1 in hiPSC-CM monolayers. MitoTEMPO (MT) (1 μM) does not significantly suppress the IFN response. Bar graphs show relative band intensity normalized to total protein loading (1-way ANOVA with Tukey’s multiple-comparison test). Lysates were from 3–5 different hiPSC-CM samples. ( C ) Inhibition of JAK/STAT signaling in hiPSC-derived engineered heart tissues (EHTs) with ruxolitinib, but not mitoTEMPO (MT), decreased the interferon response of signaling proteins STAT1, pSTAT1, IRF9, and MX1. Lysates loaded for the Western blot in C were from 3 different EHTs. ( D ) <t>Cytokine</t> secretion into the media induced by PIC, measured using a <t>human</t> <t>Proteome</t> Profiler array (inset shows exemplar blots), was greatly suppressed by Rux treatment in hiPSC-CM.
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    ( A ) Schematic of molecular mechanisms of COVID-19 and dsRNA induced IFN response. Ruxolitinib suppresses IFN-stimulated response and mitoTEMPO suppresses mitochondrial damage and oxidative stress. (Created with BioRender.com.) ( B and C ) Inhibition of JAK/STAT signaling with ruxolitinib (Rux) (1 μM) significantly suppressed PIC-mediated induction of the interferon response signaling proteins STAT1, p-STAT1, IRF9, and MX1 in hiPSC-CM monolayers. MitoTEMPO (MT) (1 μM) does not significantly suppress the IFN response. Bar graphs show relative band intensity normalized to total protein loading (1-way ANOVA with Tukey’s multiple-comparison test). Lysates were from 3–5 different hiPSC-CM samples. ( C ) Inhibition of JAK/STAT signaling in hiPSC-derived engineered heart tissues (EHTs) with ruxolitinib, but not mitoTEMPO (MT), decreased the interferon response of signaling proteins STAT1, pSTAT1, IRF9, and MX1. Lysates loaded for the Western blot in C were from 3 different EHTs. ( D ) <t>Cytokine</t> secretion into the media induced by PIC, measured using a <t>human</t> <t>Proteome</t> Profiler array (inset shows exemplar blots), was greatly suppressed by Rux treatment in hiPSC-CM.
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    ( A ) Schematic of molecular mechanisms of COVID-19 and dsRNA induced IFN response. Ruxolitinib suppresses IFN-stimulated response and mitoTEMPO suppresses mitochondrial damage and oxidative stress. (Created with BioRender.com.) ( B and C ) Inhibition of JAK/STAT signaling with ruxolitinib (Rux) (1 μM) significantly suppressed PIC-mediated induction of the interferon response signaling proteins STAT1, p-STAT1, IRF9, and MX1 in hiPSC-CM monolayers. MitoTEMPO (MT) (1 μM) does not significantly suppress the IFN response. Bar graphs show relative band intensity normalized to total protein loading (1-way ANOVA with Tukey’s multiple-comparison test). Lysates were from 3–5 different hiPSC-CM samples. ( C ) Inhibition of JAK/STAT signaling in hiPSC-derived engineered heart tissues (EHTs) with ruxolitinib, but not mitoTEMPO (MT), decreased the interferon response of signaling proteins STAT1, pSTAT1, IRF9, and MX1. Lysates loaded for the Western blot in C were from 3 different EHTs. ( D ) <t>Cytokine</t> secretion into the media induced by PIC, measured using a <t>human</t> <t>Proteome</t> Profiler array (inset shows exemplar blots), was greatly suppressed by Rux treatment in hiPSC-CM.
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    ( A ) Schematic of molecular mechanisms of COVID-19 and dsRNA induced IFN response. Ruxolitinib suppresses IFN-stimulated response and mitoTEMPO suppresses mitochondrial damage and oxidative stress. (Created with BioRender.com.) ( B and C ) Inhibition of JAK/STAT signaling with ruxolitinib (Rux) (1 μM) significantly suppressed PIC-mediated induction of the interferon response signaling proteins STAT1, p-STAT1, IRF9, and MX1 in hiPSC-CM monolayers. MitoTEMPO (MT) (1 μM) does not significantly suppress the IFN response. Bar graphs show relative band intensity normalized to total protein loading (1-way ANOVA with Tukey’s multiple-comparison test). Lysates were from 3–5 different hiPSC-CM samples. ( C ) Inhibition of JAK/STAT signaling in hiPSC-derived engineered heart tissues (EHTs) with ruxolitinib, but not mitoTEMPO (MT), decreased the interferon response of signaling proteins STAT1, pSTAT1, IRF9, and MX1. Lysates loaded for the Western blot in C were from 3 different EHTs. ( D ) <t>Cytokine</t> secretion into the media induced by PIC, measured using a <t>human</t> <t>Proteome</t> Profiler array (inset shows exemplar blots), was greatly suppressed by Rux treatment in hiPSC-CM.
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    Image Search Results


    ( A ) Schematic of molecular mechanisms of COVID-19 and dsRNA induced IFN response. Ruxolitinib suppresses IFN-stimulated response and mitoTEMPO suppresses mitochondrial damage and oxidative stress. (Created with BioRender.com.) ( B and C ) Inhibition of JAK/STAT signaling with ruxolitinib (Rux) (1 μM) significantly suppressed PIC-mediated induction of the interferon response signaling proteins STAT1, p-STAT1, IRF9, and MX1 in hiPSC-CM monolayers. MitoTEMPO (MT) (1 μM) does not significantly suppress the IFN response. Bar graphs show relative band intensity normalized to total protein loading (1-way ANOVA with Tukey’s multiple-comparison test). Lysates were from 3–5 different hiPSC-CM samples. ( C ) Inhibition of JAK/STAT signaling in hiPSC-derived engineered heart tissues (EHTs) with ruxolitinib, but not mitoTEMPO (MT), decreased the interferon response of signaling proteins STAT1, pSTAT1, IRF9, and MX1. Lysates loaded for the Western blot in C were from 3 different EHTs. ( D ) Cytokine secretion into the media induced by PIC, measured using a human Proteome Profiler array (inset shows exemplar blots), was greatly suppressed by Rux treatment in hiPSC-CM.

    Journal: JCI Insight

    Article Title: Innate immune activation and mitochondrial ROS induce acute and persistent cardiac conduction system dysfunction after COVID-19

    doi: 10.1172/jci.insight.193164

    Figure Lengend Snippet: ( A ) Schematic of molecular mechanisms of COVID-19 and dsRNA induced IFN response. Ruxolitinib suppresses IFN-stimulated response and mitoTEMPO suppresses mitochondrial damage and oxidative stress. (Created with BioRender.com.) ( B and C ) Inhibition of JAK/STAT signaling with ruxolitinib (Rux) (1 μM) significantly suppressed PIC-mediated induction of the interferon response signaling proteins STAT1, p-STAT1, IRF9, and MX1 in hiPSC-CM monolayers. MitoTEMPO (MT) (1 μM) does not significantly suppress the IFN response. Bar graphs show relative band intensity normalized to total protein loading (1-way ANOVA with Tukey’s multiple-comparison test). Lysates were from 3–5 different hiPSC-CM samples. ( C ) Inhibition of JAK/STAT signaling in hiPSC-derived engineered heart tissues (EHTs) with ruxolitinib, but not mitoTEMPO (MT), decreased the interferon response of signaling proteins STAT1, pSTAT1, IRF9, and MX1. Lysates loaded for the Western blot in C were from 3 different EHTs. ( D ) Cytokine secretion into the media induced by PIC, measured using a human Proteome Profiler array (inset shows exemplar blots), was greatly suppressed by Rux treatment in hiPSC-CM.

    Article Snippet: Using a human cytokine antibody array (Proteome Profiler, R&D Systems), we found that PIC induced the secretion of a plethora of cytokines into the media from hiPSC-CM, including a >2-fold increase in 36 of the 105 cytokines assayed ( and ).

    Techniques: Inhibition, Comparison, Derivative Assay, Western Blot