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Cobas 311 analyzer

Manufactured by Roche
Sourced in Germany

The Cobas 311 analyzer is a compact, automated clinical chemistry analyzer designed for routine laboratory testing. It performs a range of diagnostic tests on various sample types, including serum, plasma, and urine. The Cobas 311 provides reliable and efficient results to support clinical decision-making.

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Lab products found in correlation

4 protocols using cobas 311 analyzer

1

Capillary and Venous Blood Analysis

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Capillary blood glucose was measured using Glucometer (one touch ultra mini ACCU-CHEK®Aviva). [16] [17] [18] Venous blood specimens were obtained via venipuncture for blood urea nitrogen and creatinine in a sterile plain bottle at the hospital's central chemical pathology laboratory where the blood chemistry auto-analyzer model cobas 311 analyzer (F. Hoffman-La Roche Ltd) was used.
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2

Plasma Biomarkers of Oxidative Stress

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Plasma lactate was measured using a Cobas 311 analyzer (Roche, Mannheim, Germany). Plasma protein carbonyls were measured using a commercially available ELISA kit (BioCell Corporation, Auckland, New Zealand) according to the manufacturer's instructions. Reduced glutathione (GSH) was measured in blood samples using the Bioxytech GSH/GSSG-412 assay kit (OxisResearch, Portland, OR, USA) according to the manufacturer's instructions.
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3

Mouse Serum Biochemical Markers

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Serum was collected from mouse eyeballs after centrifugation. Biochemical indicators of alanine aminotransferase (ALT), aspartate aminotransferase (AST), total protein (TP2), uric acid (UA), high-density lipoprotein 3 (HDCL3) and high-density lipoprotein 4 (HDCL4) were tested by a cobas 311 analyzer (Roche diagnostics) according to guidelines provided by the manufacturer.
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4

Measuring Serum Urate in REGARDS Study

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Baseline serum urate was measured using a colorimetric assay on a Cobas 311 analyzer (Roche, Basel, Switzerland) in a sample of REGARDS study participants following a case-cohort design (14 (link)). Specifically, serum urate was measured in a sample of 1,104 REGARDS study participants randomly selected using an age-sex-race-stratified sampling approach (i.e., the random sub-cohort), and in all participants who experienced sudden cardiac death without a prior CHD event (n=435) or a CHD event excluding sudden cardiac death (n=1,612) through December 31, 2013 (i.e., the cases). After excluding participants with a history of CHD and those with missing serum urate at baseline, the final analytic dataset for the current analysis included 840 REGARDS study participants from the random sub-cohort, 235 participants with sudden cardiac death, and 851 participants with incident CHD (Figure 1).
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