Cobas pentra system

Manufactured by Horiba

The COBAS PENTRA system is an automated hematology analyzer designed for clinical laboratory use. It provides comprehensive blood cell analysis, including red blood cell, white blood cell, and platelet measurements. The system utilizes advanced technology to ensure accurate and reliable results.

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Lab products found in correlation

Nefa hr set, by Fujifilm (2 mentions) Abx triglyceriden cp, by Horiba (2 mentions) Abx glucose hk cp, by Horiba (2 mentions) Cobas pentra centrifugal spectrophotometer, by Horiba (2 mentions) 2470 automatic gamma counter wizard2 wallac, by PerkinElmer (2 mentions) Autodelfia system, by PerkinElmer (2 mentions) Glycerol kit, by R-Biopharm (2 mentions) Human insulin specific ria kit, by Merck Group (2 mentions) Cobas 6000 system, by Roche (2 mentions)

2 protocols using cobas pentra system

Blood Biomarkers Measurement Protocol

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Blood was collected from the antecubital vein for analyses of several blood variables. Plasma concentrations of free fatty acids (NEFA-HR set; Wako Chemicals), free glycerol (Glycerol kit; R-Biopharm), total glycerol (ABX Triglyceriden CP; Horiba ABX), and glucose (ABX Glucose HK CP; Horiba ABX) were measured on a COBAS PENTRA centrifugal spectrophotometer (Horiba ABX). Plasma triglyceride concentrations were calculated by subtracting free glycerol from the total glycerol concentrations, and serum insulin was analyzed on a Gamma Counter (2470 Automatic Gamma Counter Wizard2 Wallac; Perkin-Elmer) with a Human Insulin specific RIA kit (Millipore). Plasma norepinephrine and adrenaline were analyzed by using reagents from Recipe Chemicals and Instruments with HPLC through electrochemical detection. Serum TSH was measured by an Electrochemiluminescence Immunoassay Kit on a COBAS 6000 system (Roche Diagnostica), and free thyroxine (FT4) was analyzed by a solid-phase time-resolved fluoroimmunoassay kit on an AutoDELFIA system (PerkinElmer). Plasma inflammatory marker C- reactive protein (CRP) was measured with a particle-enhanced immunoturbidimetric assay on a COBAS PENTRA system (Horiba ABX). For detailed description see S1 Text—Study Protocol.

Broeders E.P., Vijgen G.H., Havekes B., Bouvy N.D., Mottaghy F.M., Kars M., Schaper N.C., Schrauwen P., Brans B, & van Marken Lichtenbelt W.D. (2016). Thyroid Hormone Activates Brown Adipose Tissue and Increases Non-Shivering Thermogenesis - A Cohort Study in a Group of Thyroid Carcinoma Patients. PLoS ONE, 11(1), e0145049.

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Comprehensive Metabolic Panel Analysis

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Blood was collected from the antecubital vein for analyses of several blood variables. Plasma concentrations of free fatty acids (NEFA-HR set; Wako Chemicals), free glycerol (Glycerol kit; R-Biopharm), total glycerol (ABX Triglyceriden CP; Horiba ABX), and glucose (ABX Glucose HK CP; Horiba ABX) were measured on a COBAS PENTRA centrifugal spectrophotometer (Horiba ABX). Plasma triglyceride concentrations were calculated by subtracting free glycerol from the total glycerol concentrations, and serum insulin was analyzed on a Gamma Counter (2470 Automatic Gamma Counter Wizard2 Wallac; Perkin-Elmer) with a Human Insulin specific RIA kit (Millipore). Serum TSH was measured by an Electrochemiluminescence Immunoassay Kit on a COBAS 6000 system (Roche Diagnostica), and free thyroxine (FT4) was analyzed by a solid-phase time-resolved fluoroimmunoassay kit on an AutoDELFIA system (PerkinElmer). Plasma inflammatory marker C-reactive protein (CRP) was measured with a particle-enhanced immunoturbidimetric assay on a COBAS PENTRA system (Horiba ABX). BA concentrations were determined in plasma by phase liquid chromatography associated to tandem mass spectrometry (LC-MS/MS, in Multiple Reaction Monitoring [MRM] mode) after extraction by protein precipitation. The use of internal deutered standards allowed the quantification.

Broeders E.P., Nascimento E.B., Havekes B., Brans B., Roumans K.H., Tailleux A., Schaart G., Kouach M., Charton J., Deprez B., Bouvy N.D., Mottaghy F., Staels B., van Marken Lichtenbelt W.D, & Schrauwen P. (2015). The Bile Acid Chenodeoxycholic Acid Increases Human Brown Adipose Tissue Activity. Cell metabolism, 22(3).

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