Description
Rat MIF (Macrophage Migration Inhibitory Factor) ELISA Kit
The Rat MIF (Macrophage Migration Inhibitory Factor) ELISA Kit is a cutting-edge assay meticulously developed for the accurate quantification of MIF levels in various rat biological samples. Macrophage Migration Inhibitory Factor (MIF) is a key regulatory cytokine implicated in numerous physiological and pathophysiological processes, including inflammation, immunity, and cell migration. This state-of-the-art ELISA kit offers researchers a powerful tool to investigate the role of MIF in modulating immune responses, inflammatory pathways, and disease progression.
With exceptional sensitivity and specificity, our ELISA kit ensures precise and reproducible results, enabling a deeper understanding of MIF's functions in health and disease. Trust in Assay Genie's high-quality ELISA kit for robust performance and reliable measurements in your research studies.
| Product Name: | Rat MIF (Macrophage Migration Inhibitory Factor) ELISA Kit |
| Product Code: | AEES00475 |
| Assay Type: | Sandwich |
| Format: | 96T |
| Assay Time: | 3.5h |
| Reactivity: | Rat |
| Detection Range: | 1.56-100 ng/mL |
| Sensitivity: | 0.94 ng/mL |
| Sample Type & Sample Volume: | Serum, plasma and other biological fluids, 100?L |
| Specificity: | This kit recognizes Rat MIF in samples. No significant cross-reactivity or interference between Rat MIF 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 Rat MIF concentrations in Serum, plasma and other biological fluids. |
This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat MIF. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Rat MIF and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Rat MIF, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat MIF. You can calculate the concentration of Rat MIF in the samples by comparing the OD of the samples to the standard curve.
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level Rat MIF were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level Rat MIF were tested on 3 different plates, 20 replicates in each plate.
| Intra-assay Precision | Inter-assay Precision | |||||
| Sample | 1 | 2 | 3 | 1 | 2 | 3 |
| n | 20 | 20 | 20 | 20 | 20 | 20 |
| Mean (ng/mL) | 5.36 | 12.21 | 34.78 | 5.20 | 12.74 | 32.86 |
| Standard deviation | 0.30 | 0.54 | 1.14 | 0.33 | 0.70 | 1.56 |
| CV (%) | 5.60 | 4.42 | 3.28 | 6.35 | 5.49 | 4.75 |
Recovery
The recovery of Rat MIF spiked at three different levels in samples throughout the range of the assay was evaluated in various matrices.
| Sample Type | Range (%) | Average Recovery (%) |
| Serum(n=8) | 91-105 | 97 |
| EDTA plasma (n=8) | 94-105 | 99 |
| Cell culture media (n=8) | 85-98 | 92 |
| 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 100?L standard or sample to the wells. Incubate for 90 min at 37°C |
| 2. | Discard the liquid, immediately add 100?L Biotinylated Detection Ab working solution to each well. Incubate for 60 min at 37°C |
| 3. | Aspirate and wash the plate for 3 times |
| 4. | Add 100?L HRP conjugate working solution. Incubate for 30 min at 37°C. Aspirate and wash the plate for 5 times |
| 5. | Add 90?L Substrate Reagent. Incubate for 15 min at 37°C |
| 6. | Add 50?L Stop Solution |
| 7. | Read the plate at 450nm immediately. Calculation of the results |
