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Tr213

Manufactured by Randox
Sourced in United Kingdom

The TR213 is a clinical chemistry analyzer designed for in-vitro diagnostic testing. It provides automated analysis of a variety of biochemical parameters in biological samples. The TR213 utilizes spectrophotometric techniques to deliver accurate and reliable results.

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5 protocols using tr213

1

Plasma and Tissue Lipid Quantification

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Ten-microliter plasma samples were directly treated with 1 mL of working reagent (TR213, Randox), absorbance read at 500 nm after 5-min incubation at 37 °C. Hepatic tissue samples were first extracted with a proper amount of solvent (chloroform: methanol 2: 1, v/v) and Triton x-100 added. Extracts were vacuumed and reconstituted with the working reagent (TR213, Randox). Subsequent procedures were the same as those for serum samples [15 (link)].
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2

Hepatic Triglyceride Quantification

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Total triglyceride (TG) were extracted from liver tissues using Folch solution (chloroform-methanol, 2:1 v/v), dried and dissolved in 100% EtOH47 (link). Hepatic lipid extracts were assayed for TG levels using commercial assay kits (Randox, TR213).
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3

Serum Biomarker Measurement Protocol

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Blood serum was obtained by centrifuging at 1000 × g for 10 min. Total triglycerides (TR213, Randox Laboratories, Antrim, UK), total cholesterol (CH201, Randox Laboratories, Antrim, UK), aspartate aminotransferase (AST) (AS521, Randox Laboratories, Antrim, UK), alanine aminotransferase (ALT) (AL520, Randox Laboratories, Antrim, UK), gamma-glutamyl transferase (γGT) (GT523, Randox Laboratories, Antrim, UK), and alpha-fetoprotein (AFP) (AB360, Randox Laboratories, Antrim, UK), were determined using by enzymatic colorimetric methods using commercial kits (Randox Laboratories, Antrim, UK), respectively [27 (link)].
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4

Biochemical Markers Profiling of Metabolic Status

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Plasma levels of aspartate aminotransferase (AST; AS521, Randox Laboratories, Antrim, UK), alanine aminotransferase (ALT; AL520, Randox Laboratories), total cholesterol (CH201, Randox Laboratories), and triglycerides (TR213, Randox Laboratories) were determined through enzymatic colorimetric methods using commercial kits (Randox Laboratories). In addition, levels of insulin (Mercodia AB, Uppsala, Sweden) and glycosylated hemoglobin (HbA1c; Fortress Diagnostics, UK) were determined.
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5

Multiparametric Serum Lipoprotein Analysis

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Sera were analyzed by a colorimetric assay for total cholesterol (SB-1010–225, Fisher Scientific, Hampton NH) and by ELISAs for PCSK9 (MPC900, R&D Systems, Minneapolis MN) and APOB (ab230932, abcam, Cambridge UK). Serum lipoprotein fractionation assays were performed at the University of Cincinnati Mouse Metabolic Phenotyping Center. Sera were pooled from 5 mice for each genotype and fractionated by fast liquid protein chromatography (FPLC) into 50 fractions. Cholesterol (NC9343696, Fisher, Hampton NH) and triglyceride (TR213, Randox Laboratories, Crumlin UK) content in each fraction were determined using a microliter plate enzyme-based assay. Liver function tests were performed at the University of Michigan In-Vivo Animal Core (IVAC) with sera collected from individual mice using a Liasys analyzer (AMS Alliance).
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