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Meso scale discovery sector imager 2400

Manufactured by Mesoscale
Sourced in United States

The Meso Scale Discovery SECTOR Imager 2400 is a laboratory instrument designed for sensitive and precise detection and quantification of a wide range of analytes, including proteins, nucleic acids, and small molecules. The core function of the SECTOR Imager 2400 is to perform highly sensitive and quantitative electrochemiluminescence (ECL) assays. The instrument utilizes advanced optics and detection technologies to enable accurate and reproducible measurements across various applications.

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6 protocols using meso scale discovery sector imager 2400

1

Cytokine and Chemokine Profiling in HIV

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We analyzed the cytokine/chemokine levels in 21 HIV-uninfected participants and in 25 HIV-infected participants at baseline. Cytokine and chemokine levels in seminal plasma were measured using the Meso Scale Discovery SECTOR Imager 2400 (Meso Scale Discovery, Rockville, MD) multiplexing system following manufacturer's instructions. Using samples collected at 1∶6 dilution, we measured 13 cytokines and chemokines including interleukin (IL)-1α, IL-8, monocyte chemotactic protein-1 (MCP-1), Monokine induced by gamma interferon (MIG), Macrophage inflammatory protein-3 (MIP-3α), Regulated And Normal T-cell Expressed and Secreted (RANTES), IL-10, IL-17, IL-1β, IL-6, Interferon gamma-induced protein 10 (IP-10), MIP-1β and tumor necrosis Factor alpha (TNF-α). Log10-transformed cytokine levels were used in subsequent analysis.
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2

Serum Cytokine Measurement Protocol

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Serum IL-6 and TNF-α were multiplexed and measured using an electrochemilluminescence method with Meso Scale Discovery kits, and read using the Meso Scale Discovery Sector Imager 2400, following kit instructions (Meso Scale Discovery, Rockville, MD). Each subject’s samples were assayed for all cytokine markers in one run, thus using the same controls for all time points (Kiecolt-Glaser et al., 2015 (link)). Sensitivity for these serum cytokines was 0.3 pg/mL. The intra-assay coefficient of variation for IL-6 was 3.42%, and the inter-assay coefficient of variation was 8.43%; corresponding values for TNF-α were 2.59% and 8.14%.
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3

Biomarker Quantification in Serum

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Blood was collected in sterile 5 ml BD vacutainer SST II Advance tubes. After centrifugation, serum was aspirated and stored at -80°C until analysis. Before analysis, serum samples where thawed and mixed thoroughly.
sVCAM-1, E-selectin, P-selectin, thrombomodulin, sICAM-1, sICAM-3, hs-CRP, SAA, IL-6, IL-8, and TNF-α were measured with a single- or multiplex array detection system based on electro-chemiluminescence technology (Meso Scale Discovery SECTOR Imager 2400, Gaithersburg, Maryland, USA). All measurements were performed in duplicate. Inter-assay and intra‐assay variations for all the markers were <9%, except the inter-assay variation for E-selectin (10.1%), sICAM-1 (10.2%) and IL-6 (14.0%).
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4

Serum IL-6 Quantification with Electrochemiluminescence

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Serum levels of IL -6 were measured using an electrochemilluminescence method with Meso Scale Discovery kits, and read using the Meso Scale Discovery Sector Imager 2400 (see Richter, 2004 (link) for details regarding this assay technique). Each participant's stored samples were assayed for both IL-6 samples simultaneously, thus allowing thesame controls across both time points for each person. Sensitivity for the IL-6 assayswas 0.3 pg/ml. The intra -assay coefficient of variation (CV) was 1.43% and the inter-assay CV was 4.42%.
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5

Quantifying Inflammatory Biomarkers via Multiplex Assay

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Soluble vascular cellular adhesion molecule 1 (sVCAM-1), soluble E-selectin (sE-selectin), soluble P-selectin (sP-selectin), soluble Thrombomodulin (sThrombomodulin), soluble intercellular adhesion molecule 1 (sICAM-1), soluble intercellular adhesion molecular 3 (sICAM-3), high-sensitivity C-reactive protein (hs-CRP), serum amyloid A (SAA), interleukin 6 (IL-6), interleukin 8 (IL-8), and tumor necrosis factor alpha (TNF-α) were measured with a single- or multiplex array detection system based on electro-chemiluminescence technology (Meso Scale Discovery SECTOR Imager 2400, Gaithersburg, Maryland, USA). All measurements were performed in duplicate. Inter-assay and intra-assay variations for all the markers were <9%, except the inter-assay variations for sE-selectin (10.1%), sICAM-1 (10.2%), and IL-6 (14.0%).
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6

Measuring Inflammation Biomarkers in Serum

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Fasting blood samples were collected between 7:00 and 9:00 AM to control for diurnal variation. Serum levels of tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), interleukin-8 (IL-8), and interleukin-1β (IL-1β) were measured using an electrochemiluminescence method with Meso Scale Discovery kits, and read using the Meso Scale Discovery Sector Imager 2400 (Meso Scale Discovery, Rockville, MD). Sensitivity was .3 pg/mL, .4 pg/mL, and .2 pg/mL for TNF-α, IL-6, and IL-1β, respectively. The intra-assay and inter-assay CVs for TNF-α were 4.32% and 5.30%, respectively; corresponding values were 1.43% and 4.42% for IL-6 and 4.15% and 4.03% for IL-1β. Each women’s frozen samples were assayed for all cytokines in one run using the same controls for all time points for each person. Cytokine data were log transformed to better approximate normality of residuals. A z-score composite of serum cytokines was calculated to obtain a summary measure of inflammation. This method was previously used as a robust representation of overall inflammation (Alfano et al., 2017 (link); Liu et al., 2017 ; Shrout et al., 2020 (link)). The z-score composite demonstrated acceptable levels of internal consistency on average across the three visits (α = .76).
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