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Luminex multiplex bead based technology

Manufactured by R&D Systems
Sourced in United States

The Luminex® multiplex bead-based technology is a platform that enables the simultaneous measurement of multiple analytes in a single sample. The technology utilizes color-coded magnetic beads, each coated with a specific capture antibody, to allow for the detection and quantification of multiple targets in a single well or tube.

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Lab products found in correlation

3 protocols using luminex multiplex bead based technology

1

Multiplex Luminex Cytokine Assay

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Cytokines concentrations were measured in serum inactivated for 20 minutes at 56°C (13 (link)) using Luminex multiplex bead-based technology (R&D Systems) and a Bio-Plex 200 instrument (BioRad), on serum diluted to 1/2.
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2

Quantification of Cytokines and Biomarkers in BAL Fluid

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Cytokines were measured at distance using Luminex® multiplex bead-based technology (R&D Systems, Minneapolis, MN, USA) and a Bio-Plex 200® instrument (BioRad, Hercules, CA, USA), according to the manufacturers’ protocols. BAL fluid concentrations of 22 biomarkers, including inflammatory markers and cytokines/chemokines (interleukin (IL)-1Ra, IL-6, IL-7, IL-8, IL-10, IL-12/23p40, IL-13, IL-17A, interferon (IFN)-γ, tumor necrosis factor (TNF)-α, granulocyte–macrophage-colony stimulating factor (GM-CSF), RANTES, CXCL10, Serpin E1), endothelial injury (intercellular adhesion molecule-1 (ICAM-1), vascular endothelial growth factor (VEGF), von Willebrand Factor (vWF), angiopoietin (Ang)-1/2) and alveolar epithelium injury (receptor for advanced glycation end products (RAGE), surfactant protein (SP)-D, amphiregulin) biomarkers, were quantified in BAL fluid supernatant and serum and expressed in fluorescence intensities and concentrations (pg/mL).
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3

Multiplex Biomarker Profiling in ARDS

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Concentrations of 22 biomarkers were measured using Luminex® multiplex bead-based technology (R&D Systems, Minneapolis, MN, USA) in BAL fluid supernatant and serum from 70 pneumonia-related ARDS from the PICARD cohort [6 (link)]. These included inflammatory markers and cytokines/chemokines (interleukin (IL)-1Ra, IL-6, IL-7, IL-8, IL-10, IL-12/23p40, IL-13, IL-17A, interferon (IFN)-γ, tumor necrosis factor (TNF)-α, granulocyte-macrophage-colony stimulating factor (GM-CSF), RANTES, IP-10/CXCL10, and Serpin E1), endothelial injury (intercellular adhesion molecule-1 (ICAM-1), vascular endothelial growth factor (VEGF), von Willebrand Factor (vWF), and Angiopoietin (Ang)-1/2) and alveolar epithelium injury (receptor for advanced glycation end products (RAGE), surfactant protein (SP)-D, and amphiregulin). The results of quantification were expressed as fluorescence intensities.
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