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Uric Acid (UA) Colorimetric Assay Kit

  • $ 45995
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Uric Acid (UA) Colorimetric Assay Kit

SKU # E-BC-K016-M
Detection Instrument Microplate reader (680-700 nm, optimum wavelength: 690 nm)
Detection Method Colorimetric method


Product Details

Properties

Synonyms UA
Sample Type Serum, plasma, urine
Sensitivity 1.30 mg/L
Detection Range 1.30-80 mg/L
Detection Method Colorimetric method
Assay type Quantitative
Assay time 35 min
Precision Average inter-assay CV: 4% | Average intra-assay CV: 2%
Other instruments required Micropipettor, Centrifuge, Vortex mixer
Other reagents required Normal saline (0.9% NaCl), PBS (0.01 M, pH 7.4)
Storage 2-8℃
Valid period 12 months

 

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 (1.30-80 mg/L).

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

Sample type Dilution factor
Mouse serum 1-2
Rat serum 1
Human serum 1
Porcine serum 1
Dog serum 1-2
Human urine 8-10

 

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

 

Detection Principle

Uric Acid in protein-free filtrate reduce phosphotungstic acid to form tungsten blue, allantoin and carbon dioxide, the depth of blue color is proportional to the concentration of uric acid. Uric acid content can be calculated by measuring the OD value at 690 nm.

 

Kit Components & Storage

Item Component Size 1(48 T) Size 2(96 T) Storage
Reagent 1 1 g/L Uric Acid Standard 1 mL ×1 vial 1 mL ×1 vial 2-8℃, 12 months
Reagent 2 Protein Precipitator 15 mL ×1 vial 30 mL × 1 vial 2-8℃, 12 months
Reagent 3 Alkali Reagent 3 mL ×1 vial 6 mL × 1 vial 2-8℃, 12 months
Reagent 4 Phosphotungstic Acid Reagent 3 mL ×1 vial 6 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 (mg/L) 2.40 35.00 60.00
%CV 2.3 1.8 1.9


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 (mg/L) 0.10 0.40 0.76
%CV 4.4 2.1 0.7


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. (mg/L) 15 35 55
Observed Conc. (mg/L) 14.4 34.3 51.7
Recovery rate (%) 96 98 94


Sensitivity

The analytical sensitivity of the assay is 1.30 mg/L UA. 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 (mg/L) 0 10 20 30 40 50 60 80
Average OD 0.037 0.043 0.053 0.064 0.076 0.086 0.095 0.123
Absoluted OD 0 0.006 0.017 0.027 0.039 0.049 0.059 0.086