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Immulite 2000 il 6

Manufactured by Siemens
Sourced in Germany

The IMMULITE® 2000 IL-6 is a diagnostic instrument used for the quantitative determination of interleukin-6 (IL-6) levels in human serum and plasma. It is a fully automated immunoassay system that utilizes a chemiluminescent detection method.

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4 protocols using immulite 2000 il 6

1

Comprehensive Biomarker Analysis in Blood Samples

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A fasting blood test was collected from all included patients from the right antecubital vein. The evaluated parameters and biomarkers included lymphocytes (reference value (RV): cell count × 109/L), hemoglobin (RV: 12–16 g/dL), platelets (RV: 150–400 count × 109/L), lactate dehydrogenase (LDH) level (135–250 U/L), serum creatinine (RV: 0.5–1.1 mg/dL), aspartate aminotransferase (AST) (RV < 32 U/L), (RV < 40 U L); D-dimer (RV < 500 ng/dL), serum ferritin (RV: 15–150 ng/mL), interleukin-6 (RV: <5.9 pg/mL), high-sensitivity C-reactive protein (hs-CRP) (RV 1–5 mg/L), NT-ProBNP (0–125 pg/mL), and high-sensitivity Troponin T (hs-TnT) (RV: <14 pg/mL).
All tests were performed in a certified clinical laboratory (ISO 9001:2015). Inflammatory markers were evaluated using a particle-enhanced immunoturbidimetric, colorimetric (e501 Module Analyzer®, Roche Diagnostics, Basel, Switzerland) immunoassay system on IMMULITE® 2000 for interleukin-6 (IMMULITE® 2000 IL-6, Siemens Healthcare Diagnostic, Marburg, Germany). Cardiac biomarkers were measured by electrochemiluminescence immunoassay with a cobas® 6000 c 601 analyzer (Roche Diagnostics, Basel, Switzerland). D-dimer results were obtained by a turbidimetric test using an ACL TOP 500® hemostasis testing system (Werfen Company, Cuenca, Spain).
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2

Comprehensive Clinical Laboratory Analysis

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We carried out all tests at our certified clinical laboratory (ISO 9001:2015). White blood cells, lymphocyte, and monocyte counts were performed on Sysmex XN-1000® analyzer using the manufacture's reagents (Sysmex Corporation, Japan). Alanine aminotransferase (ALT), aspartate aminotransferase (AST), lactate dehydrogenase (LDH), LDL-c, HDL-c, TC, and TG were tested on Roche Cobas 8100 sampling system analyzer (Module Cobas® c 702, Roche Diagnostics, Switzerland) using manufacture's reagents. The methodology for direct LDL-c, HDL-c, and TC methods are based on a standard homogeneous enzymatic colorimetric assay. We tested interleukin 6 (IL6) on IMMULITE® 2000 immunoassay system using the manufacture's luminescent immunoassay reagents (IMMULITE® 2000 IL6, Siemens Healthcare Diagnostic, Germany). Procalcitonin (PCT) measurement in plasma was performed by electrochemiluminescence immunoassay on a chemistry analyzer (Cobas 6000, Roche Diagnostics) limit of detection, as below 0.02 ng/ml. We measured serum C-reactive protein (CRP) by particle enhanced immunoturbidimetric (e501 Module Analyser, Roche Diagnostics). The limit of detection was set below 0.3 mg/L.
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3

Correlation of Ella IL-6 with IMMULITE and Evidence Investigator

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EllaTM IL-6 correlation with IMMULITE® 2000 IL-6 (Siemens Healthineers, Frimley, UK) and Evidence Investigator™ (Randox, Crumlin, UK). Cytokine and Growth Factors High-Sensitivity Array showed comparable data with R2 values of 0.98 and 0.98 respectively.
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4

Biomarker Profiling in Clinical Laboratory

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We carried out all tests at a certified clinical laboratory (ISO 9001:2015). Ferritin and serum high-sensitivity C-reactive protein (hs-CRP) were measured by particle enhanced immunoturbidimetric and colorimetric assay, respectively (e501 Module Analyser®, Roche Diagnostics, Basel, Switzerland). Interleukin-6 (IL-6) was tested on IMMULITE® 2000 immunoassay system (IMMULITE® 2000 IL-6, Siemens Healthcare Diagnostic, Marburg, Germany). Quantification of biomarkers, such as the N-terminal prohormone of brain natriuretic peptide (NT-ProBNP) and the high-sensitivity T troponin (hs TnT) in plasma, were measured by electrochemiluminescence immunoassay with the analyzer Cobas® 6000 c 601 (Roche Diagnostics, Basel, Switzerland). D-dimer was obtained by a turbidimetric test with the ACL Top 500® hemostasis testing system (Werfen Company, Cuenca, Spain).
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