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Triglyceride (TG) Colorimetric Assay Kit (Single Reagent, GPO-PAP Method) (E-BC-K261-M)

All Size Price Qty
500Assays $ 360.00
96T $ 120.00
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For research use only.

Detection 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.
Synonyms TG
Sample Type Serum,Plasma,Tissue
Detection Method Colorimetric method
Detection Instrument Microplate reader (510 nm)
Research Area Metabolic Diseases ,  Glycolysis And Lipid Metabolism ,  Energy Metabolism
Other Reagents Required Normal saline (0.9% NaCl), PBS (0.01 mol/L, pH 7.4), Isopropanol (AR), Anhydrous ethanol
Storage This product can be stored at 2-8°C for 12 months with shading light.
Valid Period 12 months
Sensitivity 0.14 mmol/L
Detection Range 0.14-10 mmol/L
Precision inter-assay CV: 9.2% | intra-assay CV: 4.1%
Sample Volume 2.5 μL
Assay Time 30 min

The recommended dilution factor for different samples is as follows (for reference only):

Sample Type Dilution Factor
Human serum 1
Mouse serum 1
Rat plasma 1
10% Mouse liver tissue homogenate 1
10% Mouse kidney tissue homogenate 1
10% Mouse heart tissue homogenate 1

The diluent is normal saline (0.9% NaCl) or PBS (0.01 M, pH 7.4). For the dilution of other sample types, please do pretest to confirm the dilution factor.

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