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QuicKey Human AMH(Anti-Mullerian Hormone) ELISA Kit

  • Cat.No.:E-TSEL-H0018

  • Reactivity: Human

To Purchase E-TSEL-H0018

Size:
  • 96T
  • 48T
  • 24T
  • 96T*5
Price: $390
Qty:

Properties

Format 24T, 48T, 96T, 96T*5, 96T*10
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.

Assay Procedures

elisa assay procedure 1

1. Add 100μL standard or sample to the wells. Incubate for 90 min at 37°C

elisa assay procedure 2

2. Discard the liquid, immediately add 100μL Biotinylated Detection Ab working solution to each well. Incubate for 60 min at 37°C

elisa assay procedure 3

3. Aspirate and wash the plate for 3 times

elisa assay procedure 4

4. Add 100μL HRP conjugate working solution. Incubate for 30 min at 37°C. Aspirate and wash the plate for 5 times

elisa assay procedure 5

5. Add 90μL Substrate Reagent. Incubate for 15 min at 37°C

elisa assay procedure 6

6. Add 50μL Stop Solution

elisa assay procedure 7

7. Read the plate at 450nm immediately. Calculation of the results

Citations

  1. ENDOCRINOLOGY (2022) IF: 4.736
    Scream sound induced chronic psychological stress results in diminished ovarian reserve in adult female rat

    DOI: 10.1210/endocr/bqac042

    Sample: serum
  2. TOXICOLOGY LETTERS (2020) IF: 3.569
    Possible role of n-hexane as an endocrine disruptor in occupationally exposed women at reproductive age

    DOI: 10.1016/j.toxlet.2020.04.022

    Sample: serum
  3. TOXICOLOGY AND APPLIED PHARMACOLOGY (2019) IF: 3.585
    High copper levels in follicular fluid affect follicle development in polycystic ovary syndrome patients: Population-based and in vitro studies

    DOI: 10.1016/j.taap.2019.01.008

    PMID: 30641075

    Sample: Serum,Cell culture medium
  4. International Journal of General Medicine (2021) IF: 2.466
    Correlation of Serum Anti-Mullerian Hormone (AMH) Level on Ovarian Volume in Women with Endometrioma

    DOI: 10.2147/IJGM.S272071

    Sample: serum
  5. European Journal of Obstetrics & Gynecology and Reproductive Biology (2016) IF: 1.662
    Serum anti-Müllerian hormone levels in euthyroid adolescent girls with Hashimoto's thyroiditis: relationship to antioxidant status

    DOI: 10.1016/j.ejogrb.2016.06.002

    Sample: Serum
  6. European Journal of Obstetrics & Gynecology and Reproductive Biology (2017) IF: 1.666
    Diminished ovarian reserve in women with transfusion-dependent beta-thalassemia major: Is iron gonadotoxic?

    DOI: 10.1016/j.ejogrb.2017.06.038

    PMID: 28732253

    Sample: Serum
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