Triglycerides Reagents
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Description
METHOD
Enzymatic colorimeter test
PRINCIPLE Triglycerides are determined after enzymatic hydrolysis with lipases. The quinonemine indicator is formed from hydrogen peroxide, 4-aminophenazone, and 4-chlorophenol under the catalytic influence of peroxidase.
SAMPLE:
Serum. Heparinised plasma or EDTA plasma.
Stability : 3 days at 2 - 8°C. 3 months at -20°C
REAGENTS
Reagnet I : Enzyme regent
Reagent II : Buffer reagent
Triglyceride Standard : 200 mg/dl.
Enzymatic colorimeter test
PRINCIPLE Triglycerides are determined after enzymatic hydrolysis with lipases. The quinonemine indicator is formed from hydrogen peroxide, 4-aminophenazone, and 4-chlorophenol under the catalytic influence of peroxidase.
SAMPLE:
Serum. Heparinised plasma or EDTA plasma.
Stability : 3 days at 2 - 8°C. 3 months at -20°C
REAGENTS
Reagnet I : Enzyme regent
Reagent II : Buffer reagent
Triglyceride Standard : 200 mg/dl.
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Triglycerides Reagents