Follicle-Stimulating Hormone (FSH)

PDB ID: 9YXD. Source: RCSB Protein Data Bank. For illustration purposes only.

VeriLumenTM 促卵泡激素

The VeriLumenTM FSH Rapid Test is a fluorescence immunochromatographic assay for the quantitative detection of follicle-stimulating hormone (FSH) in human whole blood, plasma, or serum samples. FSH is a pituitary gonadotropin involved in the regulation of reproductive function, including follicular development in females and spermatogenesis in males. Its concentration is widely used in the clinical assessment of fertility status, ovarian reserve, and pituitary-gonadal axis function. The assay provides rapid quantitative results to support timely clinical evaluation in laboratory and point-of-care settings.

This test is mainly used in the clinical evaluation of reproductive and endocrine function, supporting assessment of infertility, menstrual disorders, menopause status, and testicular dysfunction. In children, it supports the evaluation of delayed or precocious puberty. Quantitative FSH measurement may assist healthcare professionals in hormonal evaluation when interpreted together with clinical findings and other laboratory data.

Ref. Code 808184
Analyte Follicle-Stimulating Hormone (FSH)
Format Fluorescence lateral flow immunoassay (cassette format)
Quantitative / Qualitative Quantitative
Time to Result 10 minutes
Measuring Range 0.7–100 mIU/mL
Reference Value
Sample Range (mIU/mL)
Male Normal 1.50–12.40
Female Follicular phase 4.46–12.43
Ovulatory period 4.86–20.96
Luteal phase 1.96–7.70
Climacterium 22.70–130.00
R2 ≥ 0.95
Storage Conditions 2–30°C
Shelf Life 18 months
Certificate CE
Sample Types Human whole blood, plasma or serum
Sample Volume 100μL
Collection Method Venous blood
Sample Stability Stable for testing within 1 hour at room temperature (as validated)
Acceptable Anticoagulants EDTA / Heparin / Citrate (as applicable)
Notes on Handling Specimens should be collected and handled using standard laboratory procedures. Use fresh samples when possible and avoid hemolyzed, lipemic, or contaminated specimens.
Detection Method Quantitative fluorescence immunochromatography
Antibody Format Monoclonal / sandwich
Signal Generation Fluorescence signal (fluorescent-labeled immunochromatography)
Reading Method Instrument-based
Mechanism The assay is based on a fluorescence immunochromatographic sandwich principle, in which follicle-stimulating hormone (FSH) present in the sample binds to specific fluorescently labeled anti-FSH antibodies during capillary migration along the membrane. The resulting antigen–antibody complexes are captured by immobilized antibodies at the test region, and the fluorescence signal is measured and correlated with the FSH concentration in the specimen.
Tests per Kit 10/25/50 Tests
Dimension of Kit Box 21 × 13.5 × 8 cm
Kits per Carton 48 Kits
Tests per Carton (Bulk) 1200 Tests
G.W. per Carton (Boxed) 23.2 kg
G.W. per Carton (Bulk) 26.2 kg
Carton Dimension 67 × 57.5 × 39 cm
Carton Volume 0.15 CBM
Packaging Format Individual sealed test kits / bulk configuration (as applicable)
Items Included - Test cassette
- Desiccant
- Sample diluent
- ID chip
- Instructions for Use
Storage & Shipping Conditions Standard ambient transport; store according to product label requirements

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