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Biochemical analyzer

Manufactured by Abbott
Sourced in United States

The Biochemical Analyzer is a laboratory instrument used for the quantitative analysis of various biochemical components in a sample. It functions by detecting and measuring the concentration of specific substances, such as proteins, enzymes, and metabolites, in a given sample.

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3 protocols using biochemical analyzer

1

Biomarkers for Pediatric Organ Damage

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Liver damage was diagnosed if the biochemical analyzer (Abbott Laboratories, Abbott Park, IL, USA) showed abnormal values of total bilirubin (TBil), indirect bilirubin (IBil), serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), and/or alkaline phosphatase (ALP); similarly, myocardial damage was diagnosed if there were elevated levels of serum creatine kinase (CK), creatine kinase (CK) isoenzyme MB (CK-MB), and/or lactate dehydrogenase (LDH). Levels of C-reactive protein (CRP) were also detected by the biochemical analyzer (Abbott). Blood cell count analysis was performed using a Mindray BC-6900 hematology analyzer (Mindray Medical International Ltd., Shenzhen, China). The reference values of these markers were set by children’s hospital. Differences of various indicators in children of different ages were analyzed.
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2

Biomarker Detection Assay Protocol

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The serum levels of CEA and Fer were detected using a chemiluminescence immunoassay (Abbott Laboratories, Chicago, IL, USA) and their associated reagents, while the levels of CRP were detected using a biochemical analyzer (Abbott Laboratories). Blood counts were performed using a Mindray BC-6900 blood hematology analyzer (Mindray medical international limited, Shenzhen, China) and its associated reagents. The levels of IL-6 were detected using a Roche automatic electrochemiluminescence immunoassay and its associated reagents (Roche diagnostic Company limited, Basel, Switzerland). The PCT levels were assessed using a mini-Vidas immunofluorescence analyzer (BioMerieus Company, Craponne, France), The D-dimer level was assessed using a Stago automatic coagulometer (Stago diagnostic Company limited, Paris, France).
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3

Comprehensive Metabolic Profile Assessment

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The fasting venous blood sample was collected after admission. Blood urea nitrogen (BUN), creatinine (Cr), ALT, AST, total cholesterol, high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-c), and triglycerides (TG) were measured using a biochemical analyzer (Abbott, Abbott Park, IL). Glycated hemoglobin A1c (HbA1c) was measured by a HLC-T OSOH 723 G7 automated glycated hemoglobin analyzer. Plasma concentrations of highly sensitive C-reactive protein (hs-CRP) was determined using commercially available kits (Finland Orion Diagnostica Company, Espoo, Finland). Fasting blood glucose (FBG) and 2-hour postprandial blood glucose (P2BG) were measured by a glucometer (Johnson & Johnson).
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