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Human magnetic luminex assay

Manufactured by Bio-Techne
Sourced in United Kingdom, United States

The Human Magnetic Luminex Assay is a multiplex immunoassay platform that allows for the simultaneous measurement of multiple analytes in a single sample. The assay utilizes magnetic beads coated with specific capture antibodies to capture and detect target analytes in a sample. The assay is designed to provide quantitative results for a range of human-specific proteins, cytokines, and other biomolecules.

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7 protocols using human magnetic luminex assay

1

Plasma IL-6 Quantification by Luminex Assay

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The plasma level of IL-6 was determined using a human Magnetic Luminex Assay (Bio-Techne, Abingdon, Oxon, UK) and a Magpix Luminex instrument (Luminex Corp, Austin, Texas, US) according to the manufacturer’s instruction.
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2

Luminex-based Protein Quantification

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Medium was sampled from the OrganoPlate and added to the pre-ordered plate containing the analyte-specific capture antibodies, which bind to the analytes of interest according to the kit protocol. The Human Magnetic Luminex® Assay was used (bio-techne, #LXSAHM-11). Samples were analyzed on the MAGPIX xPONENT® software. The samples were normalized and compared to standards.
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3

Comprehensive Metabolic and Cytokine Profiling

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Levels of glucose, insulin, and lipid parameters were determined using standard methods in certified laboratories. FFA and glycerol levels were measured using enzymatic colorimetric kits (Randox, Crumlin, United Kingdom). Cytokines in plasma, LAT fluid and conditioned media were assessed by ELISA (Duosets, R&D Systems, Abingdon, United Kingdom) and/or Luminex (High-Sensitivity T cell panel, Merck-Millipore, Germany and Human Magnetic Luminex Assay, Bio-Techne, Minneapolis, MN, USA).
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4

Multiplex Cytokine Profiling in Plasma

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Plasma levels of various cytokines, chemokines and adipokines were determined using a human Magnetic Luminex Assay (Bio-Techne, Abingdon, Oxon, UK) and a Magpix Luminex instrument (Luminex Corp, Austin, TX, USA) according to manufacturer’s instructions. The following parameters were determined with the corresponding assay ranges: CC-chemokine ligand (CCL) 2 (30.9–7500 pg/mL), CCL13 (4.94–1200 pg/mL), intercellular adhesion molecule 1 (ICAM-1) (7000–1,700,000 pg/mL), IL-1ra (28.8–7000 pg/mL), IL-2 (0.64–28.00 pg/mL), IL-6 (0.85–35.00 pg/mL), IL-8 (1.6–11.70 pg/mL), IL-10 (0.24–10.0 pg/mL), IL-18 (18.5–4500 pg/mL), leptin (494–120,000 pg/mL), resistin (53.5–13,000 pg/mL), TNF-α (8.23–2000 pg/mL) and vascular endothelial growth factor (VEGF) (8.23–2000 pg/mL). All measured values for the cytokines were within the assay range and the corresponding standard curve.
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5

Multiplex Biomarker Profiling in Plasma

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Plasma levels of IL-1β, IL1ra, IL-6, IL-15, TNF-α, CX3CL1/fractalkine, adiponectin, and resistin were determined using a human Magnetic Luminex Assay (Bio-Techne, Abingdon, Oxon, UK) and a Magpix Luminex instrument (Luminex Corp, Austin, TX, USA) according to the manufacturer’s instructions.
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6

Cytokine profiling of HIV antigen stimulation

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PBMCs from healthy HIV-negative donors were resuspended at a concentration of 1 × 106/mL and were stimulated with 100μL of supernatant of gp160 (either WT or S375W)-expressing cells treated or not with temsavir (10 μM) or BNM-III-170 (50 μM). After stimulation, cells were centrifuged and the supernatants were collected. Triplicates of supernatant were analyzed using a customized Human Magnetic Luminex Assay (Bio-Techne, Minneapolis, MN, USA) to detect the following cytokines: IL-1β, IL-6, IL-10, IL-18, IL-23, IL-27, TNF-α, TSLP, CCL2, CCL4, CCL20, CXCL2 and CXCL13.
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7

Comprehensive Serum Cytokine Analysis

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Serum cytokines were analyzed using a “Human Magnetic Luminex assay” (Bio-techne, Minneapolis, Minnesota, US) with 22 analytes: APRIL, BAFF, CCL2, CCL3, CD40L, CD138, CXCL9, CXCL10, IL-1β, IL-2, IL-4 IL-6, IL-10, IL-12, IL-13, IL-17, IL-18, IL-21, IL-33, IFN-α, IFN-γ, and TNF. Frozen patient serum samples were thawed and diluted before the experiment with an equal amount of dilution buffer and the experiment was performed according to the manufacturer’s instructions. All samples were measured on a Lifematch Fluoroanalyzer (Tepnel Life Science PLC, Wythenshawe, UK) equipped with XPonent 3.1 Software (Luminex Corporation, Austin, Texas, US). Serum TPO was quantified by ELISA using Human Thrombopoietin Quantikine ELISA Kit (R&D Systems, Minneapolis, Minnesota, US) according to manufacturer’s protocol.
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