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QuicKey Human AMH(Anti-Mullerian Hormone) ELISA Kit
SKU: E-TSEL-H0018
QuicKey Human AMH(Anti-Mullerian Hormone) ELISA Kit
| Detection Range | 0.31-20 ng/mL |
| Sensitivity | 0.19 ng/mL |
Product Details
Properties
| Format | 96T |
| Assay time | 2.5h |
| Sample type | serum and plasma |
| Sample volume | 100μL |
| Sample size | Run up to 46 samples in duplicate and 30 samples in triplicate |
| Storage | 2-8℃ |
| Interpretation | Detection range: 0.31-20 ng/mL Sensitivity: 0.19 ng/mL |
| Application | Quantitative determination of Human AMH concentrations in human serum, plasma and other biological fluids |
| Reproducibility | Both intra-CV and inter-CV are < 10% |
Test Principle
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 Human AMH. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Human AMH 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 Human AMH, 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 Human AMH. You can calculate the concentration of Human AMH in the samples by comparing the OD of the samples to the standard curve.
Kit Components and Storage
An unopened kit can be stored at 2-8℃ for six months. After test, the unused wells and reagents should be stored according to the table below.
| Item | Specifications | Storage conditions after test |
|---|---|---|
| Micro ELISA Plate (Dismountable) | 96T: 8 wells ×12 strips 48T: 8 wells ×6 strips |
2-8℃, 1 month |
| Reference Standard | 96T: 2 vials 48T: 1 vial |
Discard unused reconstituted standard and dilutions |
| Reference Standard & Sample Diluent | 1 vial, 20 mL | 2-8℃ |
| Biotinylated Detection Ab Working Solution | 1 vial, 6 mL | |
| HRP Conjugate Diluent | 1 vial, 14 mL | |
| Concentrated Wash Buffer (25×) | 1 vial, 30 mL | |
| Concentrated HRP Conjugate (100×) | 96T: 1 vial, 120 μL 48T: 1 vial, 60 μL |
2-8℃ (Protect from light) |
| Substrate Reagent | 1 vial, 10 mL | |
| Stop Solution | 1 vial, 10 mL | 2-8℃ |
| Plate Sealer | 5 pieces | |
| Product Description | 1 copy | |
| Certificate of Analysis | 1 copy |
Technical Data:
Precision
Intra-assay Precision: 3 samples with low, mid range and high level Human AMH were tested 20 times on one plate, respectively.
Inter-assay Precision: 3 samples with low, mid range and high level Human AMH were tested on 3 different plates, 20 replicates in each plate, respectively.
| Intra-assay Precision | Inter-assay Precision | |||||
|---|---|---|---|---|---|---|
| Sample | 1 | 2 | 3 | 1 | 2 | 3 |
| n | 20 | 20 | 20 | 20 | 20 | 20 |
| Mean (ng/mL) | 0.93 | 1.81 | 8.21 | 0.99 | 1.77 | 7.99 |
| Standard deviation | 0.06 | 0.1 | 0.43 | 0.05 | 0.07 | 0.3 |
| CV (%) | 6.84 | 5.79 | 5.26 | 5.09 | 4.18 | 3.71 |
Recovery
The recovery of Human AMH 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) | 90-102 | 96 |
| EDTA plasma(n=8) | 91-103 | 98 |
Target Information
Background
1. van Disseldorp J, Faddy M J, Themmen A P N, et al. Relationship of Serum Antimüllerian Hormone Concentration to Age at Menopause [J]. Obstetrical & Gynecological Survey, 2008, 63(10): 642-643.
2. Hampl R, Snajderova M, Mardesic T. Antimüllerian hormone (AMH) not only a marker for prediction of ovarian reserve [J]. Physiological research, 2011, 60(2): 217.
Assay Procedures
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1. Add 100μL standard or sample to the wells. Incubate for 90 min at 37°C |
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2. Discard the liquid, immediately add 100μL Biotinylated Detection Ab working solution to each well. Incubate for 60 min at 37°C |
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3. Aspirate and wash the plate for 3 times |
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4. Add 100μL HRP conjugate working solution. Incubate for 30 min at 37°C. Aspirate and wash the plate for 5 times |
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5. Add 90μL Substrate Reagent. Incubate for 15 min at 37°C |
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6. Add 50μL Stop Solution |
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7. Read the plate at 450nm immediately. Calculation of the results |