CLIA Kit for 8-Hydroxydeoxyguanosine (8-OHdG) Pan-species (General) Competition CLIA

8OHdG; 7,8-Dihydro-8-Oxo-2'-Deoxyguanosine; 7,8-Dihydro-8-Oxodeoxyguanosine; 8-Hydroxy-2'-Deoxyguanosine; 8-Oxo-DG

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  • CLIA Kit for 8-Hydroxydeoxyguanosine (8-OHdG) Packages (Simulation)
  • CLIA Kit for 8-Hydroxydeoxyguanosine (8-OHdG) Packages (Simulation)
  • CLIA Kit for 8-Hydroxydeoxyguanosine (8-OHdG) Results demonstration
  • CCA660Ge.jpg Typical Standard Curve
  • Certificate ISO9001: 2008, ISO13485: 2003 Registered


Matrices listed below were spiked with certain level of 8-Hydroxydeoxyguanosine (8-OHdG) and the recovery rates were calculated by comparing the measured value to the expected amount of 8-Hydroxydeoxyguanosine (8-OHdG) in samples.

Matrix Recovery range (%) Average(%)
serum(n=5) 87-101 91
EDTA plasma(n=5) 89-103 96
heparin plasma(n=5) 93-103 101


Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level 8-Hydroxydeoxyguanosine (8-OHdG) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level 8-Hydroxydeoxyguanosine (8-OHdG) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%


The linearity of the kit was assayed by testing samples spiked with appropriate concentration of 8-Hydroxydeoxyguanosine (8-OHdG) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Sample 1:2 1:4 1:8 1:16
serum(n=5) 85-101% 86-95% 79-97% 85-101%
EDTA plasma(n=5) 88-95% 79-94% 81-99% 80-96%
heparin plasma(n=5) 98-105% 87-98% 87-99% 79-94%


The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.

Reagents and materials provided

Reagents Quantity Reagents Quantity
Pre-coated, ready to use 96-well strip plate 1 Plate sealer for 96 wells 4
Standard 2 Standard Diluent 1×20mL
Detection Reagent A 1 Assay Diluent A 1×12mL
Detection Reagent B 1×120µL Assay Diluent B 1×12mL
Reagent Diluent 1×300µL Substrate B 1×2mL
Substrate A 1×10mL Instruction manual 1
Wash Buffer (30 × concentrate) 1×20mL

Assay procedure summary

1. Prepare all reagents, samples and standards;
2. Add 50µL standard or sample to each well.
    And then add 50µL prepared Detection Reagent A immediately.
    Shake and mix. Incubate 1 hour at 37°C;
3. Aspirate and wash 3 times;
4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
5. Aspirate and wash 5 times;
6. Add 100µL Substrate Solution. Incubate 10 minutes at 37°C;
7. Read RLU value immediately.

CLIA Kit for 8-Hydroxydeoxyguanosine (8-OHdG)

Test principle

The microplate provided in this kit has been pre-coated with a monoclonal antibody specific to 8-Hydroxydeoxyguanosine (8-OHdG). A competitive inhibition reaction is launched between biotin labeled 8-Hydroxydeoxyguanosine (8-OHdG) and unlabeled 8-Hydroxydeoxyguanosine (8-OHdG) (Standards or samples) with the pre-coated antibody specific to 8-Hydroxydeoxyguanosine (8-OHdG). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of 8-Hydroxydeoxyguanosine (8-OHdG) in the sample. Then the mixture of substrate A and B is added to generate glow light emission kinetics. Upon plate development, the intensity of the emitted light is reverse proportional to the 8-Hydroxydeoxyguanosine (8-OHdG) level in the sample or standard.


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