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High sensitivity quantikine kit

Manufactured by R&D Systems
Sourced in United States

The High Sensitivity Quantikine kit is a quantitative sandwich immunoassay designed for the measurement of low concentration analytes in various sample types. The kit utilizes the Quantikine platform and provides a sensitive and reproducible method for analyte quantification.

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2 protocols using high sensitivity quantikine kit

1

Biomarker Assessment in Sleep Disorder

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For the diagnostic PSG, all subjects went to bed at 10 pm and were naturally awakened between 5 am and 6 am. Venous blood samples were collected from all subjects between 5 am and 6 am just after awakening from PSG and were immediately put on ice. Serum was separated within 2 h of collection and samples were stored at −80 °C until analysis. Serum levels of CRP were measured using a latex particle-enhanced immunoturbidimetric assay [26 (link)]. Serum IL-6 and TNF-α levels were measured using an enzyme-linked immunosorbent assay (High Sensitivity Quantikine kit, R&D Systems, Minneapolis, MN) that could detect concentrations as low as 0.2 pg/mL and 0.5 pg/mL, respectively. Values were measured in duplicate and the average value was used for analysis.
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2

Cardiovascular Disease Risk Assessment

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All participants underwent clinical and laboratory evaluations at baseline to identify the presence and severity of cardiovascular risk factors as well as subclinical and clinical cardiovascular disease. The diagnosis of prevalent cardiovascular diseases at baseline and during follow up was centrally adjudicated.16 (link) The definitions of hypertension, diabetes, dyslipidemia, and hyperuricemia used in this study are provided in the Supplemental Methods. Collection of blood samples at baseline was performed via venipuncture after a 12-hour fast. Further details on sample processing are available in the Supplemental Methods and previous publications.16 (link)–18 (link) Plasma IL-6 levels were measured by enzyme-linked immunosorbent assay (ELISA, High Sensitivity Quantikine kit, R&D Systems, Minneapolis, MN, USA). The plasma samples used for IL-6 ELISA were prepared using ethylenediaminetetraacetic acid (EDTA) and were run in duplicates. The detectable limit was 0.10 pg/mL, the intra-assay coefficient of variability was 6.3% and the inter-assay coefficient of variability was 7%.19 (link),20 (link)
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