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Triglycerides lq

Manufactured by Spinreact
Sourced in Spain

Triglycerides-LQ is a laboratory reagent kit designed for the quantitative determination of triglycerides in human serum or plasma samples. It is a colorimetric assay that measures the concentration of triglycerides using an enzymatic method.

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5 protocols using triglycerides lq

1

Liver Enzyme and Lipid Profiling

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Lipase, amylase and aspartate aminotransferase (AST) activity were determined in plasma by the LIPASE-LQ, AMYLASE-LQ and GOT (AST)-LQ, respectively, (Spinreact, Girona, Spain). The procedures were performed according to the indications of the kit.
Triglycerides and total lipids were determined in liver tissue by the TRIGLYCERIDES-LQ and TOTAL LIPIDS, respectively (Spinreact, Girona, Spain). The procedures were performed according to the indications of the kit in liver homogenate in PBS (100 mg/mL). Results were normalized by protein concentration.
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2

Adipose Tissue Analysis in Rats

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After 25 weeks, rats from both groups were weighed, fasted 12 h, and sacrificed. Blood samples were collected using K+EDTA as anticoagulant. Retroperitoneal adipose tissue was collected and weighed. Plasma was obtained by blood centrifugation (3000 rpm during 15 minutes at 4°C) and stored at –70°C until needed. Glucose was measured with a commercial enzymatic kit (DCL-glucose oxidase Diagnostic Chemical Limited de Mexico, Mexico). Insulin was determined with a commercial rat specific radioimmunoassay kit (Linco Research, Inc., Missouri, USA) with 0.1 ng/mL sensitivity and intra- and interassay coefficients of variation of 5 and 10%, respectively. Triglycerides and cholesterol were determined with commercially available procedures (Spinreact cholesterol-LQ and triglycerides-LQ; Spinreact S.A. Girona, Spain). HDL-cholesterol was measured by enzymatic procedures (Hitachi 902 analyzer; Hitachi LTD, Tokyo, Japan). Accuracy and precision of lipid measurements in our laboratory are under periodic surveillance as recommended by the Centers for Disease Control and Prevention (Atlanta, GA, USA). Plasma endotoxin levels were determined with GenScript Toxin Chromogenic LAL Endotoxin according to the manufacturer's instructions.
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3

Quantification of Metabolic Biomarkers

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Quantification of glucose (Glucose-LQ, Spinreact, Girona, Spain), triglycerides (Triglycerides-LQ, Spinreact, Girona, Spain), and uric acid (Sekisui Diagnostics, Burlington, MA, USA) was performed using commercial kits according to the manufacturer’s instructions.
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4

Enzymatic Serum Biomarker Measurement

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Serum glucose and triglyceride levels were assessed using commercial kits based on a enzymatic colorimetric method (Glucose-TR and Triglycerides-LQ, Spinreact, Girona, Spain). Serum leptin and adiponectin levels were measured using enzyme-linked immunosorbent assay kits (Merck Millipore, Madrid, Spain) following the manufacturer’s instructions.
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5

Enzymatic Triglyceride Quantification

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Liver samples (40–50 mg) were extracted in 1 ml isopropanol. After centrifugation at 4 °C at 10000 rpm for 15 min, 10-μl aliquots of supernatant were added to 200 μl reagent (Triglycerides-LQ, Spinreact, Girona Spain) for enzymatic colorimetric determination of triglyceride concentration.
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