Description
Product Name: | T (Testosterone) ELISA Kit |
Product Code: | AEES00014 |
Assay Type: | Competitive |
Format: | 96T |
Assay Time: | 2.0h |
Detection Range: | 0.31-20 ng/mL |
Sensitivity: | 0.17 ng/mL |
Sample Type & Sample Volume: | Serum, plasma, urine, saliva, 50μL |
Specificity: | This kit recognizes T in samples. No significant cross-reactivity or interference between T and analogues was observed. |
Reproducibility: | Both intra-CV and inter-CV are < 10%. |
Application: | This ELISA kit applies to the in vitro quantitative determination of T concentrations in serum, plasma, urine, saliva. |
This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with T. During the reaction, T in the sample or standard competes with a fixed amount of T on the solid phase supporter for sites on the Biotinylated Detection Ab specific to T. Excess conjugate and unbound sample or standard are washed away, and Avidin-Horseradish Peroxidase (HRP) conjugate are added to each micro plate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns from blue to yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of T in tested samples can be calculated by comparing the OD of the samples to the standard curve.
Kit Components: | An unopened kit can be stored at 2-8℃ for 1 month. If the kit is not supposed to be used within 1 month, store the components separately according to the following conditions once the kit is received.
|
1. | Add 50μL standard or sample to the wells, immediately add 50μL Biotinylated Detection Ab working solution to each well. Incubate for 45 min at 37°C |
2. | Aspirate and wash the plate for 3 times |
3. | Add 100μL HRP conjugate working solution. Incubate for 30 min at 37°C. Aspirate and wash the plate for 5 times |
4. | Add 90μL Substrate Reagent. Incubate for 15 min at 37°C |
5. | Add 50μL Stop Solution |
6. | Read the plate at 450nm immediately. Calculation of the results |