Rat MYO (Myoglobin) ELISA Kit
- SKU:
- AEES00309
- Product Type:
- ELISA Kit
- ELISA Type:
- Sandwich
- Size:
- 96 Assays
- Reactivity:
- Rat
- Sensitivity:
- 0.38 ng/mL
- Range:
- 0.63-40 ng/mL
- Sample Type:
- Serum, plasma and other biological fluids
Description
Rat MYO (Myoglobin) ELISA Kit
The Rat Myoglobin (MYO) ELISA Kit is a cutting-edge assay designed for the precise and quantitative detection of myoglobin levels in various rat biological samples. Myoglobin, a vital protein found in muscle cells, plays a crucial role in storing and transporting oxygen to tissues. It serves as an indicator of muscle damage and is particularly relevant in conditions involving skeletal or cardiac muscle injuries. This advanced ELISA kit provides researchers with a reliable tool to explore myoglobin dynamics, offering insights into muscle health, injury, and disease.
With exceptional sensitivity and specificity, this kit ensures accurate and reproducible results, enabling thorough investigations into myoglobin-related processes. Manufactured under rigorous quality control standards, this kit delivers robust performance and user-friendly operation, making it an ideal choice for high-quality research applications.
Product Name: | Rat MYO (Myoglobin) ELISA Kit |
Product Code: | AEES00309 |
Assay Type: | Sandwich |
Format: | 96T |
Assay Time: | 3.5h |
Reactivity: | Rat |
Detection Range: | 0.63-40 ng/mL |
Sensitivity: | 0.38 ng/mL |
Sample Type & Sample Volume: | Serum, plasma and other biological fluids, 100μL |
Specificity: | This kit recognizes Rat MYO in samples. No significant cross-reactivity or interference between Rat MYO 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 MYO 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 MYO. 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 MYO 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 MYO, 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 MYO. You can calculate the concentration of Rat MYO 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 MYO were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level Rat MYO 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) | 2.20 | 4.40 | 14.10 | 2.10 | 4.80 | 13.70 |
Standard deviation | 0.10 | 0.20 | 0.80 | 0.10 | 0.20 | 0.50 |
CV (%) | 4.55 | 4.55 | 5.67 | 4.76 | 4.17 | 3.65 |
Recovery
The recovery of Rat MYO 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) | 88-103 | 95 |
EDTA plasma (n=8) | 87-104 | 95 |
Cell culture media (n=8) | 87-101 | 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 100μL standard or sample to the wells. Incubate for 90 min at 37°C |
2. | Discard the liquid, immediately add 100μL 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 100μL HRP conjugate working solution. Incubate for 30 min at 37°C. Aspirate and wash the plate for 5 times |
5. | Add 90μL Substrate Reagent. Incubate for 15 min at 37°C |
6. | Add 50μL Stop Solution |
7. | Read the plate at 450nm immediately. Calculation of the results |