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Home / Assay Kits

Triglyceride (TG) Colorimetric Assay Kit (Single Reagent, GPO-PAP Method)

SKU : BHE10308204

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Elabscience Biotechnology Co.,Ltd

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Mfr.No.	E-BC-K261-M
Assay Time	30 min
Assay Type	QuantitatIVe
Detection Range	0.14-10 mmol/L
Inter-cv (%)	9.2
Intra-cv (%)	4.1
Recovery	105
Sample Type	plasma, cells and tissue, Serum
Sensitivity	0.14 mmol/L
Test Principle	Triglycerides (TG) can be hydrolyzed by lipoprotein lipase into glycerol and free fatty acids. Glycerol produces glycerol-3-phosphate and ADP under the catalysis of glycerol kinase (GK). Glycerol-3-phosphate produces hydrogen peroXide under the action of glycerol phosphate oXidase (GPO). In the presence of 4-aminoantipyrine and phenol, hydrogen peroXide is catalyzed by peroXidase (POD) to produce quinones which is proportional to the content of TG.

Research Area	Lipids metabolism

Dilutions	Itis recommended to take 2~3 samples with expected large difference to dopre-experiment before formal experiment and dilute the sample according to theresult of the pre-experiment and the scavengingcapacity detection range (10-50%). The recommended dilution factor for different samples is as follows(for reference only): Sample type Dilution factor, Human serum Dog serum Rat serum Cynomolgus monkey serum 10% Rat spleen tissue homogenate 10% Mouse liver tissue homogenate 10% Rat kidney tissue homogenate 10% Rat lung tissue homogenate 1. Note: Thediluent is double distilled water.
Storage	2-8°C
Valid Period	6 Months

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SKU	Supplier No.	Size	Your price	Quantity
BHE10308204	E-BC-K261-M	96T	$120		Add to Cart

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