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Triglyceride Colorimetric Assay Kit (Single Reagent, GPO-PAP Method)– MSE Supplies LLC

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

SKU: E-BC-K238-96

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

SKU # E-BC-K238
Detection Instrument Microplate reader (510 nm), Biochemistry analyzer (510 nm)
Detection method Colorimetric method


Product Details

Properties

Synonyms TG
Sample Type Serum, plasma, cells, culture supernatant
Detection Range 0-9.04 mmol/L
Detection Method Colorimetric method
Assay type Quantitative
Assay time 20 min
Storage 2-8℃
Valid period 12 months


Images

N A M Omar et al investigate the effect of high intakes of fructose and galactose, with or without added fructooligosaccharides (FOS), on metabolism factors, inflammation, and gut integrity markers in rats. Triglyceride (TG) level in rat plasma was determined using TG colorimetric assay kit (E-BC-K238).

Plasma TG level shows no significant differences with different diets (P<0.05).

 

Detection Principle

The color depth of the generated quinones is directly proportional to the triglyceride content. The absorbance values of the standard tube and the sample tube are measured respectively, and the triglyceride content in the sample can be calculated.

 

Kit Components & Storage

Item Component Size (96 T) Storage
Reagent 1 Enzyme Working
Solution
25 mL × 1 vial 2-8℃, 12 months, shading light
Reagent 2 2.26 mmol/L Glycerinum Standard 0.1 mL × 1 vial 2-8℃, 12 months, shading light

Microplate 96 wells No requirement

Plate Sealer 2 pieces

 

Note: The reagents must be stored strictly according to the preservation conditions in the above table. The reagents in different kits cannot be mixed with each other. For a small volume of reagents, please centrifuge before use, so as not to obtain sufficient amount of reagents.

 

Technical Data:

Parameter:

Intra-assay Precision

Three human serum samples were assayed in replicates of 20 to determine precision within an assay (CV = Coefficient of Variation).

Parameters Sample 1 Sample 2 Sample 3
Mean (mmol/L) 1.50 5.00 7.50
%CV 4.4 3.5 4.4


Inter-assay Precision

Three human serum samples were assayed 20 times in duplicate by three operators to determine precision between assays.

Parameters Sample 1 Sample 2 Sample 3
Mean (mmol/L) 1.50 5.00 7.50
%CV 9.0 9.3 9.4


Recovery

Take three samples of high concentration, middle concentration and low concentration to test the samples of each concentration for 6 times parallelly to get the average recovery rate of 105%.

Parameters Sample 1 Sample 2 Sample 3
Expected Conc. (mmol/L) 0.35 5.3 9.2
Observed Conc. (mmol/L) 0.4 5.7 9.4
Recovery rate (%) 105 108 102

 

Sensitivity

The analytical sensitivity of the assay is 0.14 mmol/L. This was determined by adding two standard deviations to the mean O.D. obtained when the zero standard was assayed 20 times, and calculating the corresponding concentration.