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Total Antioxidant Capacity (T-AOC) Colorimetric Assay Kit– MSE Supplies LLC

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Total Antioxidant Capacity (T-AOC) Colorimetric Assay Kit

SKU: E-BC-K136-M-500

  • $ 42595



Total Antioxidant Capacity (T-AOC) Colorimetric Assay Kit

SKU # E-BC-K136-M
Detection Instrument Microplate reader (500-520 nm, optimum wavelength: 520 nm)
Detection method Colorimetric method


Product Details

Properties

Synonyms T-AOC
Sample Type Serum, plasma, whole blood, tissue, cells, cell culture supernatant
Sensitivity 0.62 U/mL
Detection Range 0.62-190.43 U/mL
Detection Method Colorimetric method
Assay type Enzyme Activity
Assay time 50 min
Precision Average inter-assay CV: 5.600% | Average intra-assay CV: 4.800%
Other instruments required Micropipettor, Centrifuge, Incubator, Vortex mixer
Other reagents required Normal saline (0.9% NaCl), PBS (0.01 M, pH 7.4)
Storage 2-8℃
Valid period 12 months

 

Images

D-A Dumitras et al investigate the antioxidant capacity of rhodoxanthin that can inhibit tumor growth. Total antioxidant capacity (T-AOC) in mouse plasma was determined using T-AOC colorimetric assay kit (E-BC-K136-M).

The capacity of antioxidant was significantly increased by rhodoxanthin 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 (0.62-190.43 U/mL).

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

Sample type Dilution factor
Human serum 1
Human urine 1-2
10% Rat liver tissue homogenate 1
10% Epipremnum aureum tissue homogenate 1
HepG2 cells 1
HepG2 cell culture supernatant 1

 

Note: The diluent is normal saline (0.9% NaCl) or PBS (0.01 M, pH 7.4).

 

Detection Principle

A variety of antioxidant macromolecules, antioxidant molecules and enzymes in a system can eliminate all kinds of reactive oxygen species and prevent oxidative stress induced by reactive oxygen species. The total level reflect the total antioxidant capacity in the system. Many antioxidants in the body can reduce Fe3+ to Fe2+ and Fe2+ can form stable complexes with phenanthroline substance. The antioxidant capacity (T-AOC) can be calculated by measuring the absorbance at 520 nm.

 

Kit Components & Storage

Item Component Size 1(48 T) Size 2(96 T) Storage
Reagent 1 Buffer Solution 6 mL × 1 vial 12 mL × 1 vial 2-8°C, 12 months
Reagent 2 Chromogenic Agent Powder ×1 vial Powder × 2 vials 2-8°C, 12 months, shading light
Reagent 3 Ferric Salt Stock Solution 0.2 mL × 1 vial 0.4 mL × 1 vial 2-8°C, 12 months, shading light
Reagent 4 Ferric Salt Diluent 4 mL × 1 vial 8 mL × 1 vial 2-8°C, 12 months
Reagent 5 Stop Solution 1.25 mL × 1 vial 1.25 mL × 2 vials 2-8°C, 12 months
Reagent 6 Clarificant 1.25 mL × 1 vial 1.25 mL × 2 vials 2-8°C, 12 months
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 (U/mL) 3.50 64.50 138.50
%CV 5.1 4.7 4.6


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 (U/mL) 3.50 64.50 138.50
%CV 5.3 5.7 5.8

 

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 96%.

Standard 1 Standard 2 Standard 3
Expected Conc. (U/L) 22.5 84.6 164.5
Observed Conc. (U/L) 22.3 80.4 154.6
Recovery rate (%) 99 95 94

 

Sensitivity

The analytical sensitivity of the assay is 0.62 U/mL. 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.