Diagnostic Kit for β-hCG (Immunofluorescence Assay) is intended for in-vitro quantitative determination of β-human chorionic gonadotropin (β-hCG) in human whole blood, serum, or plasma.
CE marked
For professional in vitro diagnostic use
Working only with MPQuanti® Immunofluorescence Analyzer
Linear working range: 2-200,000 mIU/mL, R≥0.990
Test results should be interpreted at 15 minutes
for the diagnosis of β-human chorionic gonadotropin (β-hCG) to evaluate
the pregnant in women
Product Description
Diagnostic Kit for β-hCG is based on fluorescence immunoassay technology.
The test cassette includes anti-β-hCG antibody conjugated fluorophores and capture reagents coated on the membrane.
The Specimen moves from Specimen pad to absorbent pad. If the specimen contains β-hCG, it attaches to the fluorescent microspheres-conjugated anti-β-hCG antibodies. Then the complex will be captured by the capture antibodies coated on the nitrocellulose membrane (Test line). The concentration of β-hCG in the Specimen correlates linearly with the fluorescence signal intensity captured on the T line. According to the fluorescence intensity of the test and standard curve, the concentration of β-hCG in the Specimen can be calculated by the MP Fluorescent Immunoassay Analyzer to show β-hCG concentration in specimen.
The β-hCG Test Cassette should only be used by approved medical professionals.
Usage Statement
For professional in vitro diagnostic use only.
Should not be used as the sole criterion for treatment decisions.
Usage Statement
For professional in vitro diagnostic use only