Human FSH (Follicle Stimulating Hormone) ELISA Kit

SKU:BHE10303621
Research Validated
Overview
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FSH (Human) ELISA kit for quantitative measurement, in serum, plasma and other biological fluids (Sandwich format). HRP-colorimetric detection with standard-curve quantification. Sensitivity: 0.94 mIU/mL.
Assay Type Sandwich ELISA
Sample Type Serum
Sensitivity 0.94 mIU/mL
Detection Range 1.56-100 mIU/mL
Species Human
Assay Time 3 h 30 min
Detection Method Colorimetric (TMB/HRP)
Options selector
Catalog no. Size
E-EL-H1143_24T 24 T
E-EL-H1143_48T 48 T
E-EL-H1143_96T 96 T
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size (3) - 24 T, 48 T, 96 T
  • Lead time: varies by selected option.
  • Storage: 2-8℃,12 months
  • Shipping: cold-chain shipment (typically with ice packs).
  • Upon receipt: refrigerate upon receipt at 2–8°C.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
UniProt # P01225
Applications
  • ELISA
Sensitivity 0.94 mIU/mL
Detection range 1.56-100 mIU/mL
Detection method
  • Colorimetric method
  • ELISA
  • Sandwich
Assay time
  • 3 h 30 min
Storage 2-8℃,12 months
Shipping Ice packs
Catalog no. (Mfr.) E-EL-H1143
Main SKU BHE10303621

Scientific Background

This ELISA kit applies to the in vitro quantitative determination of Human FSH concentrations in serum, plasma and other biological fluids.

Assay 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 FSH. 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 FSH 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 FSH, 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 FSH. You can calculate the concentration of Human FSH in the samples by comparing the OD of the samples to the standard curve.

Performance Specifications

Sensitivity 0.94 mIU/mL
Detection Range 1.56-100 mIU/mL
Total Assay Time 3 h 30 min
Compatible Sample Types Serum, plasma and other biological fluids
Species Reactivity Human
Detection Method Sandwich
Precision (CV) Both intra-CV and inter-CV are < 10%.
Recovery Rate 80%-120%
Storage 2-8℃,12 months

✓ Research-Grade Validation

Specificity

This kit recognizes Human FSH in samples. No significant cross-reactivity or interference between Human FSH and analogues was observed

Safety & Regulatory

Research Use Only (RUO). This product is intended for research purposes only and is not approved for diagnostic, therapeutic, or clinical use.

Handle reagents in accordance with institutional biosafety guidelines. Refer to the Safety Data Sheet (SDS) for complete hazard and handling information. Contains components that may require special disposal procedures per local regulations.

What sample types are compatible with this FSH ELISA kit?

This kit is validated for use with Serum, plasma and other biological fluids. For unlisted matrices (e.g., tissue lysate, urine), perform a spike-and-recovery experiment to confirm assay performance before generating reportable data. Sample dilution in the kit's provided diluent is recommended to minimize matrix interference.

What is the detection limit for FSH?

The minimum detectable concentration (sensitivity) of this kit is 0.94 mIU/mL. Values below this threshold should be reported as below the limit of detection (<LOD) and should not be extrapolated from the standard curve.

How long does the complete assay take?

The total assay time from sample addition to absorbance reading is approximately 3 h 30 min, including all incubation, wash, and substrate steps. Hands-on time is typically 1–2 hours; most steps involve passive plate incubation. Plan the assay as a single uninterrupted session for best results.

What reagents and materials are included in the kit?

Standard components of this Sandwich ELISA Kit typically include: pre-coated microplate (96-well strip format), lyophilized or liquid recombinant FSH standard, detection antibody, streptavidin-HRP conjugate, TMB substrate, stop solution, wash buffer concentrate, and sample/standard diluent. Refer to the kit insert or datasheet for the exact component list and storage requirements.

What instrument is required to read the assay?

This kit uses colorimetric (TMB/HRP) detection and requires a standard microplate absorbance reader capable of measuring at 450 nm. A reference wavelength of 570 nm or 630 nm is recommended to reduce background. No specialized fluorescence or luminescence reader is needed. Ensure the instrument is calibrated and the plate is clean and free of condensation before reading.

Why is it necessary to add a protease inhibitor in tissue sample preparation during an Elisa experiment? Will it affect the detection significantly if there is no protease inhibitor?

Tissue samples may contain endogenous or exogenous proteases during processing, leading to degradation of extracted proteins. Therefore, it's necessary to add protease inhibitors during processing to ensure the integrity of target proteins. If customers can keep samples cold and handle them quickly during processing, omitting the protease inhibitor may not have a significant effect. After preparation, samples should be tested promptly or immediately aliquoted and frozen at -20°C or -80°C.

This kit is designed for the original strain of the new crown virus, and the omicron variant has not been verified. However, we have verified 26 recombinant variants of the SARS-CoV-2 spike protein through the kit. For more information, customers can refer to the kit instructions (https://file.elabscience.com/Manual/covid_19/E-EL-E605 .pdf).

What is the range of enzyme activity of your IL-2 freeze-dried powder

Currently our freeze-dried powder is a concentration unit with no information on the activity unit for the time being.

What is the principle of adding stop solution to stop color reaction in ELISA experiment?

Can’t Find What You’re Looking For? We can help you source the best match or customize an ELISA solution for your study. Options may include alternative target synonyms, different species reactivity, sample type/matrix compatibility (serum/plasma/lysate/supernatant), assay format (sandwich/competitive), sensitivity/range, detection chemistry (colorimetric/fluorescent/chemiluminescent), plate format (pre-coated/uncoated, strips vs full plate), and bulk or custom packaging. Click Talk to a Scientist to submit a request form, email us at support@biohippo.com, or explore our Research Services for additional support. Our team will be in contact with you shortly.

Activation of MT1/MT2 to Protect Testes and Leydig Cells against Cisplatin-Induced Oxidative Stress through the SIRT1/Nrf2 Signaling Pathway (2022) Cells. 10.3390/cells11101690

Identification and gene expression profiling of human gonadotrophic pituitary adenoma stem cells (2023) Acta Neuropathologica Communications. 10.1186/s40478-023-01517-w

A Standardized Asparagus Racemosus Root Extract Improves Hormonal Balance and Menstrual Health and Reduces Vasomotor Symptoms in Perimenopausal Women: A Randomized, Double-Blind, Placebo-Controlled Study (2025) Journal of the American Nutrition Association. 10.1080/27697061.2025.2510474

Assessment Between Follicular Fluid Multiple Element Concentrations and Hormonal Profiles of Women with Polycystic Ovary Syndrome (2023) Exposure and Health. 10.1007/s12403-023-00566-9

Personal exposure to particulate matter-bound toxic elements and ovarian reserve hormone levels (2025) Environmental Sciences Europe. 10.1186/s12302-025-01114-9

ANP promotes proliferation and inhibits apoptosis of ovarian granulosa cells by NPRA/PGRMC1/EGFR complex and improves ovary functions of PCOS rats (2017) Cell Death & Disease. 10.1038/cddis.2017.494

Effect of gestational exposure to arsenic on puberty in offspring female mice (2018) CHEMOSPHERE. 10.1016/j.chemosphere.2018.03.095

Evaluation of possible effects of Persea americana seeds on female reproductive hormonal and toxicity profile (2021) JOURNAL OF ETHNOPHARMACOLOGY. 10.1016/j.jep.2021.113870

Melatonin ameliorates ovarian dysfunction by regulating autophagy in PCOS via the PI3K-Akt pathway (2021) REPRODUCTION. 10.1530/REP-20-0643

High copper levels in follicular fluid affect follicle development in polycystic ovary syndrome patients: Population-based and in vitro studies (2019) TOXICOLOGY AND APPLIED PHARMACOLOGY. 10.1016/j.taap.2019.01.008

Prolonged administration of letrozole induces polycystic ovary syndrome leading to osteoporosis in rats: model development and validation studies (2025) NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY. 10.1007/s00210-025-03906-5

Folate deficiency mediates ovarian dysfunction through appetite and inflammatory pathways (2025) REPRODUCTIVE TOXICOLOGY. 10.1016/j.reprotox.2025.109016

The Effects of 8-Week Creatine Hydrochloride and Creatine Ethyl Ester Supplementation on Cognition, Clinical Outcomes, and Brain Creatine Levels in Perimenopausal and Menopausal Women (CONCRET-MENOPA): A Randomized Controlled Trial (2025) Journal of the American Nutrition Association. 10.1080/27697061.2025.2551184

The impact of dolutegravir-based combination antiretroviral therapy on the spermatozoa and fertility parameters of men living with human immunodeficiency virus (2022) ANDROLOGIA. 10.1111/and.14621

Plasminogen activator inhibitor 1 is a novel predictor in human serum/follicular fluid for diminished ovarian reserve (2025) BMC Womens Health. 10.1186/s12905-025-03710-6

A Combined Approach: Karyotyping and QF-PCR for Comprehensive Genetic Screening in Male Infertility (2026) BIOCHEMICAL GENETICS. 10.1007/s10528-026-11367-5

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