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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-K261-M-500

  • $ 30695



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

SKU # E-BC-K261-M
Detection Instrument Microplate reader (510 nm)
Detection method Colorimetric method


Product Details

Properties

Synonyms TG
Sample type Serum, plasma and tissue
Sensitivity 0.14 mmol/L
Detection range 0.14-10 mmol/L
Detection Method Colorimetric method
Assay type Quantitative
Assay time 30min
Precision Average inter-assay CV: 9.200% | Average intra-assay CV: 4.100%
Other instruments required Micropipettor, Water bath, Incubator, Vortex mixer, Centrifuge
Other reagents required Normal saline (0.9% NaCl), PBS (0.01 M, pH 7.4), Isopropanol(AR),Anhydrous ethanol
Storage 2-8℃
Valid period 12 months


Images

Y Gao et al developed a lipopeptide nanoplexes for atorvastatin transformation. Triglyceride (TG) level in mouse B16-F10 and CT-26 cell was determined using TG colorimetric assay kit (E-BC-K261-M).

E-BC-K261-M-CI.png (448×368)

Triglyceride level in cells were significantly reduced by atorvastatin treatment (***P<0.001)

 

Dilution of Sample

It is recommended to take 2~3 samples with expected large difference to do pre-experiment before formal experiment and dilute the sample according to the result of the pre-experiment and the detection range (0.14-10 mmol/L).

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

 

Note: The diluent is normal saline (0.9% NaCl) or PBS (0.01 M, pH 7.4) for serum (plasma) samples;   The diluent is anhydrous ethanol for tissue samples.

 

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.


Kit Components & Storage

Item Component Size 1 (96 T) Size 2 (500 Assays) Storage
Reagent 1 Enzyme Working Solution 25 mL ×1 vial 50 mL ×3 vials 2-8°C, 12 months
shading light
Reagent 2 2.26 mmol/L Glycerinum Standard 0.1 mL × 1 vial 0.1 mL × 5 vials 2-8°C, 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) 0.50 2.60 7.40
%CV 4.6 4.1 3.6


Inter-assay Precision

Three human serum samples were assayed 17 times in duplicate by three operators to determine precision between assays.

Parameters Sample 1 Sample 2 Sample 3
Mean (mmol/L) 0.50 2.60 7.40
%CV 9.1 8.5 10.0


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) 1.6 3.7 8.5
Observed Conc. (mmol/L) 1.7 3.8 9.3
Recovery rate (%) 104 102 109


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.


Standard Curve

As the OD value of the standard curve may vary according to the conditions of the actual assay performance (e.g. operator, pipetting technique or temperature effects), so the standard curve and data are provided as below for reference only:

Concentration
(mmol/L)
0 1 2 4 5 6 8 10
Average OD 0.084 0.219 0.332 0.635 0.752 0.874 1.144 1.375
Absoluted OD 0 0.135 0.248 0.551 0.669 0.790 1.060 1.292