This assay has high sensitivity and excellent specificity for detection of X-Ray Repair Cross Complementing 2 (XRCC2).
No significant cross-reactivity or interference between X-Ray Repair Cross Complementing 2 (XRCC2) and analogues was observed.

Matrices listed below were spiked with certain level of recombinant X-Ray Repair Cross Complementing 2 (XRCC2) and the recovery rates were calculated by comparing the measured value to the expected amount of X-Ray Repair Cross Complementing 2 (XRCC2) in samples.

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level X-Ray Repair Cross Complementing 2 (XRCC2) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level X-Ray Repair Cross Complementing 2 (XRCC2) 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 X-Ray Repair Cross Complementing 2 (XRCC2) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

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.

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to X-Ray Repair Cross Complementing 2 (XRCC2). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to X-Ray Repair Cross Complementing 2 (XRCC2). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain X-Ray Repair Cross Complementing 2 (XRCC2), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of X-Ray Repair Cross Complementing 2 (XRCC2) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

ELISA / CLIA Experiment Service

Single-component Reagents of Assay Kit
Lysis Buffer Specific for ELISA / CLIA
Quality Control of Kit
ELISA Kit Customized Service
Disease Model Customized Service
Serums Customized Service
TGFB1 Activation Reagent
Real Time PCR Experimental Service
Streptavidin
Fast blue Protein Stain solution
Single-component Reagents of FLIA Kit
Streptavidin-Agarose Beads