Triglycerides can be measured in the Clinical Research applications.
Please see examples below.
Triglycerides are normally measured in clinical pathology applications
A simple, rapid enzymatic analysis for plasma or serum triglycerides.
Plasma triglycerides are hydrolysed to glycerol and fatty acids in a rapid pre-reaction with Lipase (LP):
i)
In the presence of glycerol kinase (GK), glycerol is phosphorylated by adenosine triphosphate (ATP) forming glycerol-3-phosphate (G-3-P) which in turn is oxidised by glycerol-3-phosphate oxidase (GPO) to dihydroxyacteone phosphate (DAP) and hydrogen peroxide:
ii)
iii)
Under the conditions of the assay, reactions ii) and iii) run concurrently in the reaction chamber and the rate of oxygen consumption is directly proportional to the plasma triglyceride concentration
Samples | Serum or plasma containing heparin, EDTA or oxalate anticoagulants |
Sample Volume | 25 µl |
Analysis Time | 20 - 25 seconds (from injection) |
Linearity | 0 - 5 mmol/L (ca. 0 - 440 mg/dl) |
Reagent Stability | Shelf-life unopened: 9 months stored at 0 - 5°C. Shelf-life reconstituted: 3 - 4 weeks stored at 0 - 5°C. |