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Prolactin (PRL) Quantitative Test Cassette (Quantum Dot Fluorescence Immunochromatography)
Hormone immunoassay purchasing depends less on a catalog name than on specimen type, pack configuration, and documentation. The listed PRL cassette is a Guoke Medical fluorescence lateral-flow test for professional laboratory workflows.
Reproductive hormone testing often moves through centralized or near-patient labs where reagent format and workflow compatibility matter. This product is listed under Testing for Reproductive Hormones and is intended for professional medical, diagnostic, or laboratory use.
The stated method is quantum dot fluorescence immunochromatography with a double antibody sandwich format. It quantitatively detects PRL concentration in human whole blood, serum, or plasma. That places it among lateral-flow immunoassays that require compatible fluorescence detection, though the input does not name a reader.
Catalog details are limited: product code GKPD062 and pack norm 25 T/box. The supplier lists whole blood, serum, and plasma as specimen types. Buyers should confirm sample volume, handling requirements, calibration, and controls, because those points are not specified in the supplied listing.
Availability, pack size or configuration, compatible options, documentation, minimum order quantity, lead time, shipping, and quotation require direct contact. For tenders, validation, and inventory planning, those commercial terms can matter as much as the assay format itself.
The listing does not identify an instrument platform. Labs should check whether existing fluorescence immunoassay analyzers can read this cassette and whether its documentation meets local registration or tender requirements.
In hormone testing, the cassette is only one component. The reader platform, validation record, and document trail together determine whether a product can be adopted into routine operations.
Why it matters:
Buyers should verify specimen acceptance, reader compatibility, regulatory documents, and pack economics before committing to a PRL immunoassay format.
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