Bovine/Horse/Sheep E2 (Estradiol) ELISA Kit
- SKU:
- AEES00012
- Product Type:
- ELISA Kit
- ELISA Type:
- Competitive
- Size:
- 96 Assays
- Reactivity:
- Bovine
- Reactivity:
- Horse
- Reactivity:
- Sheep
- Sensitivity:
- 5.63 pg/mL
- Range:
- 9.37-600 pg/mL
- Sample Type:
- Serum
Description
| Product Name: | Bovine/Horse/Sheep E2 (Estradiol) ELISA Kit |
| Product Code: | AEES00012 |
| Assay Type: | Competitive |
| Format: | 96T |
| Assay Time: | 2.0h |
| Reactivity: | Bovine, Horse, Sheep |
| Detection Range: | 9.37-600 pg/mL |
| Sensitivity: | 5.63 pg/mL |
| Sample Type & Sample Volume: | Serum, plasma, 50μL |
| Specificity: | This kit recognizes E2 in samples. No significant cross-reactivity or interference between E2 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 E2 concentrations in serum, plasma. |
This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with E2. During the reaction, E2 in the sample or standard competes with a fixed amount of E2 on the solid phase supporter for sites on the Biotinylated Detection Ab specific to E2. 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 E2 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 |
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