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Cayman’s Triglyceride Colorimetric Assay Kit provides a simple, reproducible, and sensitive tool for assaying mono-, di-, and triglycerides in plasma, serum, cell culture extracts, and tissue homogenates. The Triglyceride Colorimetric Assay Kit uses the enzymatic hydrolysis of triglycerides by lipase to produce glycerol and free fatty acids. The glycerol released is subsequently measured by a coupled enzymatic reaction system. The glycerol formed in reaction 1 is phosphorylated to glycerol-3-phosphate in a reaction catalyzed by glycerol kinase. The glycerol-3-phosphate is oxidized by glycerol phosphate oxidase producing dihydroxyacetone phosphate and hydrogen peroxide (H2O2). Peroxidase catalyzes the redox-coupled reaction of H2O2 with 4-aminoantipyrine (4-AAP) and N-ethyl-N-(3-sulfopropyl)-m-anisidine (ESPA), producing a brilliant purple color. The absorbance is measured at 540 nm.
Needed but not supplied: Please download the kit booklet to verify if UltraPure Water (Milli-Q or equivalent) or any other components are needed for this assay.
WARNING This product is not for human or veterinary use.
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Lipid nanoparticle-
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Female mice have higher angiogenesis in perigonadal adipose tissue than males in response to high-
The soluble guanylate cyclase stimulator IW-
Developmental exposure to 2,2',4,4'-
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CAT-
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Multi-
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Alzheimer-
Resolving discrepant findings on ANGPTL8 in β-
Increased hepatic fatty acids uptake and oxidation by LRPPRC-
Deletion of cyclophilin D impairs b-
A small amount of dietary carbohydrate can promote the HFD-
Uridine prevents fenofibrate-
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Short-
Emodin, a naturally occurring anthraquinone derivative, ameliorates dyslipidemia by activating AMP-
Label-
Enzymatic determination of diglyceride using an iridium nano-
PTER is a N-