| Triglycerides Assay | |||
| Request package insert information | |||
| Product Features The Diazyme Triglyceride assay uses 3 µL sample and takes less than 10 min, and has an excellent correlation with the reference method recommended by the CDC. The reagents are liquid stable with a shelf life of 12 months from date of manufacture when stored @ 2°- 8°C. The on board stability is 1 month. The assay has a linear range of 0-11.3 mmol/L or 0-1000 mg/dL, and a total CV of < 5.0%. |
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 Assay PrincipleThe Diazyme Triglyceride assay is based on enzymatic reactions (GPO method) including lipproteinlipase (LPL), glycerol kinase (GK) and glycerol phosphate dehydrogenase (GPO). Triglycerides are hydrolyzed by LPL to liberate glycerol and free fatty acids. Glycerol is converted to glycerol-3-phosphate (G3P) and ADP by GK and ATP. G3P is then converted by GPO to dihydroxyacetone phosphate (DAP) and hydrogen peroxide (H2O2). H2O2 is quantified by Trinder reaction using 4-aminoantipyrine, 4-chlorophenol and hydrogen peroxidase. The reaction is monitored at 546 nm in a 2 point end manner. |
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| Intended use The Diazyme Triglyceride assay is intended for the in vitro test of triglycerides in human serum. |
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| Product | Catalog Number | Packaging | Method/Format |
| Kit (1800 Tests) | DZ144A-K | R1: 4 x 70 mL R2: 2 x 70 mL |
Colorimetric, endpoint Liquid Stable |
| Calibrator | DZ144A-CAL | 1 x 1 mL | |
| Control | DZ138A-CON | 3 x 3 mL | |
