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Au480 biochemistry analyzer

Manufactured by Beckman Coulter
Sourced in United States

The AU480 is a biochemistry analyzer from Beckman Coulter. It is designed to perform a variety of clinical chemistry tests, including but not limited to, the analysis of enzymes, electrolytes, and metabolites in biological samples.

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Lab products found in correlation

3 protocols using au480 biochemistry analyzer

1

Serum Lipid and Antioxidant Analysis

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Moisture and crude lipid in basal diet were measured according to AOAC, 1990 standard methods. Commercial kits (Leadman Co., Ltd) for triglyceride (TG), total cholesterol (TC), free fatty acid (FFA), high-density lipoprotein (HDL), low-density lipoprotein (HDL) and glucose (GLU) were used to detect serum parameters by Beckman AU480 biochemistry analyzer. The activities of glutathione peroxidase (GPX) and glutamic oxalacetic transaminase (GOT) were measured by the commercial kit (Nanjing Jiancheng Biotechnic Institute, China) according to the manufacturer’s instructions.
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2

Serum Biochemical Parameter Estimation

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The collected blood samples were used to estimate the serum biochemical parameters. Biochemical assays for determining serum urea, creatinine, uric acid, and CRP levels were performed using specific assay kits for each AU480 Biochemistry Analyzer (Beckman Coulter), following the manufacturer’s protocols.
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3

Comprehensive HIV Care Assessment Protocol

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We assessed HIV VL using the Abbott real time HIV-1 assay (Des Plaines, IL, USA), CD4 and CD8 cell counts using the Becton-Dickinson FacsCount (San Jose, CA, USA), and full blood count using a Beckman Coulter counter (Miami, FL, USA) to determine hemoglobin and absolute neutrophil count (ANC). We analyzed ALT and creatinine using a Beckman Coulter AU480 biochemistry analyzer (Miami, FL, USA). Data were captured on paper case report forms, reviewed via routine quality control checks and then transcribed into an electronic database. The number of missed ART doses since the last clinic visit approximately 3 months prior was self-reported by participants and considered adequate if ≥95% of doses were taken.
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