Estradiol (E2)

CID 5757. Source: PubChem. For illustration purposes only.

VeriLumenTM 雌二醇

The VeriLumenTM E2 Rapid Test is a fluorescence immunochromatographic assay for the quantitative detection of estradiol (E2) in human whole blood, plasma, or serum samples. Estradiol is a major estrogen hormone involved in the regulation of reproductive function, menstrual cycle activity, and ovarian physiology. Its concentration is widely used in the clinical assessment of ovarian function and endocrine status. 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 assessment and auxiliary diagnosis of ovarian disorders, supporting evaluation of ovarian function, menstrual irregularities, and reproductive health. Quantitative estradiol measurement may also assist in fertility evaluation and hormonal monitoring when interpreted together with clinical findings and other laboratory data.

Ref. Code 808180
Analyte Estradiol (E2)
Format Fluorescence lateral flow immunoassay (cassette format)
Diagnostic Readout Quantitative
Time to Result 10 minutes
Measuring Range 10–3000 pg/mL
Reference Value
Population Group E2 Reference Value (pg/mL)
Male Preadolescent 0–40.33
Adult 0–256.68
Female Preadolescent 0–32.97
Follicular phase 10.08–89.92
Ovulation period 100–500
Luteal phase 50.14–240.05
R2 ≥ 0.95
Storage Conditions 2–30°C
Shelf Life 18 months
Certificate CE, NMPA
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 / competitive
Signal Generation Fluorescence signal (fluorescent-labeled immunochromatography)
Reading Method Instrument-based
Mechanism The assay is based on a fluorescence immunochromatographic competitive principle, in which estradiol (E2) present in the sample competes with immobilized E2 analogs at the test region for binding to specific fluorescently labeled anti-E2 antibodies during capillary migration along the membrane. As the E2 concentration in the sample increases, fewer labeled antibodies bind at the test region, resulting in a fluorescence signal that is inversely proportional to the E2 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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