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milliplex map human high sensitivity t cell panel premixed 13-plex kit  (Millipore)


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    Millipore milliplex map human high sensitivity t cell panel premixed 13-plex kit
    Milliplex Map Human High Sensitivity T Cell Panel Premixed 13 Plex Kit, 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/product/high-sensitivity+milliplex+map+kit/milliplex/pm39899007-117-40-52
    Average 90 stars, based on 1 article reviews
    milliplex map human high sensitivity t cell panel premixed 13-plex kit - by Bioz Stars, 2026-10
    90/100 stars

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    Derivative Assay:

    Article Title: Influence of sickle cell disease on susceptibility to HIV infection
    Article Snippet: Serum samples were assayed using the following: High-sensitivity Milliplex Map kit (Millipore) for interleukin(IL)-1β, IL-2, IL-4, IL-5, IL-6, IL-7, IL-8, IL-10, IL-12 p70, IL-13, interferon (IFN)-γ, granulocyte macrophage stimulating factor (GM-CSF) and tumor necrosis factor (TNF)-α; Standard sensitivity Milliplex Map kit (Millipore) for endothelial growth factor (EGF), fibroblast growth factor (FGF)-2, fractalkine, IL-1α, IL-1 receptor antagonist (Ra), IL-9, IL-12(p40), IL-15, IL-17, interferon induced protein (IP)-10, monocyte chemotactic protein (MCP)-1, MCP-3, monocyte derived chemokine (MDC), macrophage inflammatory protein (MIP)-1α, MIP-1β, sIL-2 receptor a, TNF-β, and VEGF; Standard Sensitivity Panel II kit (Millipore) for CCL8/MCP-2, CCL13/MCP-4, CXCL5/ human neutrophil-activating peptide (ENA)-78, CXCL12/stromal derived factor (SDF)-1α+β, CXCL13/ B-cell attracting chemokine (BCA)-1, CCL1/I-309, IL-16, CCL15/MIP-1δ, CCL17/thymus and activation regulated chemokine (TARC), CCL21/6Ckine, CCL24/Eotaxin-2, CCL26/Eotaxin-3, CCL27/cutaneous T-cell attracting chemokine (CTACK), IL-23, leukemia inhibitory factor (LIF), thrombopoiesis stimulating factor (TPO), TNF-related apoptosis inducing ligand (TRAIL), stromal cell-derived cytokine (SCF), thymic stromal lymphopoietin (TSLP), IL-20, IL-21, IL-28A, and IL-33; Standard Sensitivity Panel III kit (Millipore) for macrophage colony stimulating factor (M-CSF), CXCL9/monokine induced by gamma (MIG), neutrophil attractant protein (NAP), CXCL6/ granulocyte chemotactic protein (GCP)-2, CXCL11/ Interferon-inducible T cell alpha chemoattractant (I-TAC), hemofiltrate CC-Chemokine (HCC)-1, CXCL19/MIP-3β, CCL20, MIP-3α, CL1/Lymphotactin, IL-11, and IL-29/IFN-λ.

    Article Title: Influence of sickle cell disease on susceptibility to HIV infection.
    Article Snippet: Serum samples were assayed using the following: High-sen- sitivity Milliplex Map kit (Millipore) for interleukin(IL)-1β, IL-2, IL-4, IL-5, IL-6, IL-7, IL-8, IL-10, IL-12 p70, IL-13, interferon (IFN)-γ, granulocyte macrophage stimulating factor (GM-CSF) and tumor necrosis factor (TNF)-α; Standard sensitivity Milliplex Map kit (Millipore) for endothelial growth factor (EGF), fibroblast growth factor (FGF)-2, fractalkine, IL-1α, IL-1 receptor antagonist (Ra), IL-9, IL-12(p40), IL-15, IL-17, interferon induced protein (IP)10, monocyte chemotactic protein (MCP)-1, MCP-3, monocyte derived chemokine (MDC), macrophage inflammatory protein (MIP)-1α, MIP-1β, sIL-2 receptor a, TNF-β, and VEGF; Standard Sensitivity Panel II kit (Millipore) for CCL8/MCP-2, CCL13/MCP-4, CXCL5/ human neutrophil-activating peptide (ENA)-78, CXCL12/stromal derived factor (SDF)-1α+β, CXCL13/ B-cell attracting chemokine (BCA)-1, CCL1/I-309, IL-16, CCL15/MIP-1δ, CCL17/ thymus and activation regulated chemokine (TARC), CCL21/6Ckine, CCL24/Eotaxin-2, CCL26/Eotaxin-3, CCL27/cutaneous T-cell attracting chemokine (CTACK), IL-23, leukemia inhibitory factor (LIF), thrombopoiesis stimulating factor (TPO), TNF-related apoptosis inducing ligand (TRAIL), stromal cell-derived cytokine (SCF), thymic stromal lymphopoietin (TSLP), IL-20, IL-21, IL-28A, and IL-33; Standard Sensitivity Panel III kit (Millipore) for macrophage colony stimulating factor (M-CSF), CXCL9/monokine induced by gamma (MIG), neutrophil attractant protein (NAP), CXCL6/ granulocyte chemotactic protein (GCP)-2, CXCL11/ Interferon-inducible T cell alpha chemoattractant (I-TAC), hemofiltrate PLOS ONE | https://doi.org/10.1371/journal.pone.0218880 April 8, 2020 3 / 16 CC-Chemokine (HCC)-1, CXCL19/MIP-3β, CCL20, MIP-3α, CL1/Lymphotactin, IL-11, and IL-29/IFN-λ.

    Activation Assay:

    Article Title: Influence of sickle cell disease on susceptibility to HIV infection
    Article Snippet: Serum samples were assayed using the following: High-sensitivity Milliplex Map kit (Millipore) for interleukin(IL)-1β, IL-2, IL-4, IL-5, IL-6, IL-7, IL-8, IL-10, IL-12 p70, IL-13, interferon (IFN)-γ, granulocyte macrophage stimulating factor (GM-CSF) and tumor necrosis factor (TNF)-α; Standard sensitivity Milliplex Map kit (Millipore) for endothelial growth factor (EGF), fibroblast growth factor (FGF)-2, fractalkine, IL-1α, IL-1 receptor antagonist (Ra), IL-9, IL-12(p40), IL-15, IL-17, interferon induced protein (IP)-10, monocyte chemotactic protein (MCP)-1, MCP-3, monocyte derived chemokine (MDC), macrophage inflammatory protein (MIP)-1α, MIP-1β, sIL-2 receptor a, TNF-β, and VEGF; Standard Sensitivity Panel II kit (Millipore) for CCL8/MCP-2, CCL13/MCP-4, CXCL5/ human neutrophil-activating peptide (ENA)-78, CXCL12/stromal derived factor (SDF)-1α+β, CXCL13/ B-cell attracting chemokine (BCA)-1, CCL1/I-309, IL-16, CCL15/MIP-1δ, CCL17/thymus and activation regulated chemokine (TARC), CCL21/6Ckine, CCL24/Eotaxin-2, CCL26/Eotaxin-3, CCL27/cutaneous T-cell attracting chemokine (CTACK), IL-23, leukemia inhibitory factor (LIF), thrombopoiesis stimulating factor (TPO), TNF-related apoptosis inducing ligand (TRAIL), stromal cell-derived cytokine (SCF), thymic stromal lymphopoietin (TSLP), IL-20, IL-21, IL-28A, and IL-33; Standard Sensitivity Panel III kit (Millipore) for macrophage colony stimulating factor (M-CSF), CXCL9/monokine induced by gamma (MIG), neutrophil attractant protein (NAP), CXCL6/ granulocyte chemotactic protein (GCP)-2, CXCL11/ Interferon-inducible T cell alpha chemoattractant (I-TAC), hemofiltrate CC-Chemokine (HCC)-1, CXCL19/MIP-3β, CCL20, MIP-3α, CL1/Lymphotactin, IL-11, and IL-29/IFN-λ.

    Article Title: Influence of sickle cell disease on susceptibility to HIV infection.
    Article Snippet: Serum samples were assayed using the following: High-sen- sitivity Milliplex Map kit (Millipore) for interleukin(IL)-1β, IL-2, IL-4, IL-5, IL-6, IL-7, IL-8, IL-10, IL-12 p70, IL-13, interferon (IFN)-γ, granulocyte macrophage stimulating factor (GM-CSF) and tumor necrosis factor (TNF)-α; Standard sensitivity Milliplex Map kit (Millipore) for endothelial growth factor (EGF), fibroblast growth factor (FGF)-2, fractalkine, IL-1α, IL-1 receptor antagonist (Ra), IL-9, IL-12(p40), IL-15, IL-17, interferon induced protein (IP)10, monocyte chemotactic protein (MCP)-1, MCP-3, monocyte derived chemokine (MDC), macrophage inflammatory protein (MIP)-1α, MIP-1β, sIL-2 receptor a, TNF-β, and VEGF; Standard Sensitivity Panel II kit (Millipore) for CCL8/MCP-2, CCL13/MCP-4, CXCL5/ human neutrophil-activating peptide (ENA)-78, CXCL12/stromal derived factor (SDF)-1α+β, CXCL13/ B-cell attracting chemokine (BCA)-1, CCL1/I-309, IL-16, CCL15/MIP-1δ, CCL17/ thymus and activation regulated chemokine (TARC), CCL21/6Ckine, CCL24/Eotaxin-2, CCL26/Eotaxin-3, CCL27/cutaneous T-cell attracting chemokine (CTACK), IL-23, leukemia inhibitory factor (LIF), thrombopoiesis stimulating factor (TPO), TNF-related apoptosis inducing ligand (TRAIL), stromal cell-derived cytokine (SCF), thymic stromal lymphopoietin (TSLP), IL-20, IL-21, IL-28A, and IL-33; Standard Sensitivity Panel III kit (Millipore) for macrophage colony stimulating factor (M-CSF), CXCL9/monokine induced by gamma (MIG), neutrophil attractant protein (NAP), CXCL6/ granulocyte chemotactic protein (GCP)-2, CXCL11/ Interferon-inducible T cell alpha chemoattractant (I-TAC), hemofiltrate PLOS ONE | https://doi.org/10.1371/journal.pone.0218880 April 8, 2020 3 / 16 CC-Chemokine (HCC)-1, CXCL19/MIP-3β, CCL20, MIP-3α, CL1/Lymphotactin, IL-11, and IL-29/IFN-λ.



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    Overall study design and multiplex <t>cytokine</t> analysis of rheumatoid arthritis (RA) peripheral blood mononuclear cells (PBMCs). (A) Workflow chart outlining the overall study design, illustrating each step from patient selection to data analysis, and highlighting the methodologies used in the extraction and analysis of PBMCs from unclassified arthritis (UA), healthy controls, ACPA-negative early RA (ACPA - eRA), and ACPA-positive early RA (ACPA + eRA). (B) Dot plot showing the serum concentration levels of interferon-γ (IFN-γ) in UA (n = 21), controls (n = 16), ACPA - eRA (n = 18), and ACPA + eRA (n = 19). The horizontal bar indicates the mean value. (C) Dot plot showing the serum concentration levels of interleukin-12 (IL-12) in UA (n = 21), controls (n = 16), ACPA - eRA (n = 17), and ACPA + eRA (n = 19). The horizontal bar represents the mean value. (D) Scatter plot illustrating the correlation between IFN-γ and IL-12 concentrations in serum samples. Statistical significance was assessed using the Kruskal–Wallis test for (B, C) and Pearson’s correlation coefficient for (D) . P-values less than 0.05 were considered significant.
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    Overall study design and multiplex <t>cytokine</t> analysis of rheumatoid arthritis (RA) peripheral blood mononuclear cells (PBMCs). (A) Workflow chart outlining the overall study design, illustrating each step from patient selection to data analysis, and highlighting the methodologies used in the extraction and analysis of PBMCs from unclassified arthritis (UA), healthy controls, ACPA-negative early RA (ACPA - eRA), and ACPA-positive early RA (ACPA + eRA). (B) Dot plot showing the serum concentration levels of interferon-γ (IFN-γ) in UA (n = 21), controls (n = 16), ACPA - eRA (n = 18), and ACPA + eRA (n = 19). The horizontal bar indicates the mean value. (C) Dot plot showing the serum concentration levels of interleukin-12 (IL-12) in UA (n = 21), controls (n = 16), ACPA - eRA (n = 17), and ACPA + eRA (n = 19). The horizontal bar represents the mean value. (D) Scatter plot illustrating the correlation between IFN-γ and IL-12 concentrations in serum samples. Statistical significance was assessed using the Kruskal–Wallis test for (B, C) and Pearson’s correlation coefficient for (D) . P-values less than 0.05 were considered significant.
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    Overall study design and multiplex cytokine analysis of rheumatoid arthritis (RA) peripheral blood mononuclear cells (PBMCs). (A) Workflow chart outlining the overall study design, illustrating each step from patient selection to data analysis, and highlighting the methodologies used in the extraction and analysis of PBMCs from unclassified arthritis (UA), healthy controls, ACPA-negative early RA (ACPA - eRA), and ACPA-positive early RA (ACPA + eRA). (B) Dot plot showing the serum concentration levels of interferon-γ (IFN-γ) in UA (n = 21), controls (n = 16), ACPA - eRA (n = 18), and ACPA + eRA (n = 19). The horizontal bar indicates the mean value. (C) Dot plot showing the serum concentration levels of interleukin-12 (IL-12) in UA (n = 21), controls (n = 16), ACPA - eRA (n = 17), and ACPA + eRA (n = 19). The horizontal bar represents the mean value. (D) Scatter plot illustrating the correlation between IFN-γ and IL-12 concentrations in serum samples. Statistical significance was assessed using the Kruskal–Wallis test for (B, C) and Pearson’s correlation coefficient for (D) . P-values less than 0.05 were considered significant.

    Journal: Frontiers in Immunology

    Article Title: Upregulation of interferon-γ response genes in monocytes and T cells identified by single-cell transcriptomics in patients with anti-citrullinated peptide antibody-positive early rheumatoid arthritis

    doi: 10.3389/fimmu.2024.1439082

    Figure Lengend Snippet: Overall study design and multiplex cytokine analysis of rheumatoid arthritis (RA) peripheral blood mononuclear cells (PBMCs). (A) Workflow chart outlining the overall study design, illustrating each step from patient selection to data analysis, and highlighting the methodologies used in the extraction and analysis of PBMCs from unclassified arthritis (UA), healthy controls, ACPA-negative early RA (ACPA - eRA), and ACPA-positive early RA (ACPA + eRA). (B) Dot plot showing the serum concentration levels of interferon-γ (IFN-γ) in UA (n = 21), controls (n = 16), ACPA - eRA (n = 18), and ACPA + eRA (n = 19). The horizontal bar indicates the mean value. (C) Dot plot showing the serum concentration levels of interleukin-12 (IL-12) in UA (n = 21), controls (n = 16), ACPA - eRA (n = 17), and ACPA + eRA (n = 19). The horizontal bar represents the mean value. (D) Scatter plot illustrating the correlation between IFN-γ and IL-12 concentrations in serum samples. Statistical significance was assessed using the Kruskal–Wallis test for (B, C) and Pearson’s correlation coefficient for (D) . P-values less than 0.05 were considered significant.

    Article Snippet: Concentrations of IFN-γ, IL-12 and IL-6, in serum samples of eRA patients were measured from using Millipore’s MILLIPLEX MAP High Sensitivity Human Cytokine multiplex kit (cat. no. HSTCMAG-28SK; Merck, Billerica, MA, USA) according to the manufacturer’s instructions.

    Techniques: Multiplex Assay, Selection, Extraction, Concentration Assay