Diagnostic Kit for Progesterone (Immunofluorescence Assay) is intended for in-vitro quantitative determination of Progesterone in human serum, and plasma.
CE marked
For professional in-vitro diagnostic use
Working only with MPQuanti® Immunofluorescence Analyzer
Linear working range: 1.4 ̴60 ng/mL, R≥0.990
Test results should be interpreted at 15 minutes
Product Description
Diagnostic Kit for Progesterone is based on fluorescence immunoassay technology. The test includes anti-Progesterone antibody coated fluorophore and progesterone antigen coated on the membrane.
The specimen moves through the strip from sample pad to absorbent pad. Progesterone in the specimen will compete with the Progesterone antigen coated on the membrane with the progesterone antibody labeled with fluorescent microspheres. The less Progesterone in the specimen, the more chance that fluorescent microspheres-conjugated anti-Progesterone antibodies can be captured by the Progesterone antigen coated on the membrane (Test line). The concentration of Progesterone in the specimen is inversely related to the intensity of the fluorescent signal captured on the T line. According to the fluorescence intensity of the test and the standard curve, the concentration of Progesterone in the specimen can be calculated by the MP Fluorescent Immunoassay Analyzer to show Progesterone concentration in specimen.
Tests should be applied by professionally trained staff working in certified laboratories at some remove from the patient and clinic at which the sample(s) is taken by qualified medical personnel.
Usage Statement
For professional in vitro diagnostic use only.