Dojindo,DPPH抗氧化剂检测试剂盒/500/D678,基于 Shimamura 等人报告的微孔板方法

身体抗氧化能力的变化与各种疾病和健康问题的发展有关。 因此,这增加了对具有抗氧化活性的食物(抗氧化食物)的期望。 高知大学的 Shimamura 等人。 开发了一种使用 DPPH(2,2-二苯基-1-苦基肼)评估抗氧化活性的方法,测量设备之间的差异很小 1)。 本产品使用基于 Shimamura 等人报告的微孔板方法。 通过手动 DPPH 测量方法和生产质量稳定的试剂盒,我们能够减少数据的可变性和试剂制备的复杂性,这是迄今为止遇到的问题。1) T. Shimamura 等人,肛门。 科学, 2014, 30, 717 – 721

Simple ProcedureDPPH and Trolox are unstable in solution. Please prepare immediately before using.DPPH content needs to be checked by measuring absorbance.Reagents necessary for measurement are inlcuded and subdivided. Begin experiments immediately with simple preparation before measurement.(Please use sonication to dissolve the DPPH Reagent.)


Measuring methodAfter preparing the reagent, add the reagent and sample to the 96-well microplate and react for 30 minutes.


Comparison with a conventional methodWhen measuring antioxidant activity with DPPH, the pH and solvent concentration in the solution affect the measurement. This product uses protocols and analysis methods to minimize these effects.

Effect of pHThe assay buffer provided with the product allows measurement at a certain pH.

Effect of sample solventThe sample volume is set to 1/10 (20 μL) of the total reaction solution. The kit is optimized so that there is no difference in the measured value even if the sample is dissolved in water or ethanol.

IC50 Value VariationIf the antioxidant capacity of a sample is analyzed using only IC50 values, the data will vary slightly in the different measurement conditions. By measuring the sample and standard substance (Trolox) simultaneously and calculating the antioxidant capacity as the Trolox equivalent activity value (TEAC), highly reproducible measurement values can be obtained.TEAC (μg TE/μg) = Trolox IC50 (μg/mL)/ Sample IC50 (μg/mL)”


Measurement ExampleConfirming differences between facilitiesAt three facilities, antioxidants were measured by the DPPH method.Gallic acid, catechin, and morin (known antioxidants) were measured with a spectrophotometer using a cuvette and calculated as a Trolox equivalent activity value (TEAC).There was nearly no difference in measured values between three facilities.Reference: T. Shimamura et al., NipponShokuhin Kagaku Kogaku Kaishi, 2007, 54, 482 – 487.

Comparison between microplate and cuvetteSimilar to the above experiment, three antioxidants were measured using a microplate and calculated as Trolox equivalent activity values. As a result, almost the same measurement results were obtained. This kit uses a microplate for measurement.

IC50 values vary, are there any precautions?
(1) Please make sure that all of the DPPH is dissolved.Please use sonication to dissolve the DPPH Reagent because it is difficult to dissolve.Transfer ethanol to the tube several times as described in the instruction manual. Confirm that the ethanol is no longer colored before use.(2) IC50 values may fluctuate greatly when the sample dilution interval is wide or when measured at the point where the inhibition curve is saturated (see below).Therefore, it is recommended that the optimal concentration range be confirmed in a preliminary experiment.
Can I dissolve DPPH by vortexing or pipetting?
Since DPPH is difficult to dissolve, it cannot be dissolved using vortex and pipetting.Be sure to use an ultrasonic cleaner because undissolved parts may cause variations in IC50.”
How many samples can I measure?

This depends on the kit size:

100 tests 500 tests
This kit contains enough reagents to measure one 96-well microplate (1 set of DPPH)Analyzing samples and standards in triplicate is recommended for accuracy.Therefore, the number of measurable samples is calculated as follows, assuming that measurement was performed at n: 3.DPPH Reagent per 1 kit is sufficient for 100 tests.Use for 1 sampleOne sample can be measured with the 100 test size kit.Number of wells used during preliminary experiment: Confirmation of optimum concentration range

Sample: 8 (dilution series of 8 points) X 3 (n: 3) = 24 wellBlank: 1 (Blank1) X 3 (n: 3) = 3 well

Number of wells used when calculating the IC50 value

Sample: 8 (dilution series of 8 points) X 3 (n: 3) = 24 well

Trolox: 4 (dilution series of 4 points) X 3 (n: 3) = 12 well

Blank: 1 (Blank1) X 3 (n: 3)= 3 well*If there is no require preliminary experiments, the additional sample measurement is possible.

This kit contains enough reagents to measure 5 96-well microplates (5 sets of DPPH)Choose the quantity used based on your experiment (ex. 500 test x1 or 100 test x5)Up to 8 samples8 samples can be measured with the 500 test size kit.Number of wells during the preliminary experiment: Confirmation of optimum concentration rangeSample: 8 (dilution series of 8 points) X 3 (n: 3) X 8 (8 samples) = 192 wellBlank: 1 (Blank1) X 3 (n: 3) X 3 (3 plates) = 9 wellNumber of wells when calculating IC50 value

Sample: 8 (dilution series of 8 points) X 3 (n: 3) X 8 (8 samples) = 192 welll

Trolox: 4 (dilution series of 4 points) X 3 (n: 3) X 5 (5 plates) = 60 well

Blank: 1 (Blank1) X 3 (n: 3) X 3 (3 plates) = 9 well

IC50 value is known: 3 samples・If the IC50 value has already been measured with our kit, 3 samples can be measured with one kit.・If the IC50 value is not measured with our kit, it is recommended to perform a preliminary experiment as an unknown sample.

Number of wells when calculating the IC50 valueSample: 8(dilution series of 8 points) X 3 (n: 3) X 3 (Sample number) = 72 wellTrolox: 4 (dilution series of 4 points) X 3 (n: 3) = 12 wellBlank: 1 (Blank1) X 3 (n: 3) = 3 well

If the reaction time until measurement is increase, will the measured value be affected?
Longer reaction times can change the readings.In order to get the good results with reproducibility, measure immediately after incubation (25 ° C, 30 minutes, dark place) as described in the manual.When measuring multiple plates, please unify the measurement time for each plate.
What should I do if my sample is opaque?
If the sample is clear after the pretreatment described in the manual, measurement is possible.