Self Test Dengue Igg Igm Rapid Test Kits Average 99% Accuracy

Self-Test Dengue Igg Igm Rapid Test Kits

Description

The Dengue IgG/IgM Rapid Test Kit (Colloidal Gold) is a self-test kit, which is used alone to produce results without using the instrument. Intended use: This kit is applicable for in vitro qualitative tests of Dengue IgG/IgM antibody in the sample of human serum, plasma, and whole blood. Clinically, this kit is mainly applicable for auxiliary diagnosis of dengue fever. Intended users: The product is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in the techniques of in vitro diagnostic procedures.

Description of the components

rapid test kit.pdf

Picture details

Principle of the assay method or the principles of operation:

By the immunochromatographic technique, this kit tests the Dengue IgG/IgM antibody through the antibody-capturing method. At the test, the treated extract is dripped into the sample injection hole of the test card. When Dengue IgG/IgM antibody exists in the test sample and its concentration is higher than the minimum detection limit, Dengue IgG/IgM antibody first forms by labeling Dengue antigen into reaction complex.

Under the chromatographic action, the reaction complex moves forwards along the nitrocellulose membrane; it is separately captured by an anti-human IgG/IgM antibody pre-coated in the test area on the nitrocellulose membrane. In the test area, one red/pink reaction line is finally formed; at this time, a positive result is indicated. On the contrary, when Dengue IgG/IgM antibody does not exist in the test sample and its concentration is lower than the minimum detection limit, the red/pink reaction line will not appear in the test area; at this time, a negative result is indicated. No matter whether Dengue IgG/IgM antibody exists in the test sample, one red/pink reaction line will be formed in the quality control area (C). The red/pink reaction line displayed in the quality control area (C) is the judgment criteria for whether the chromatographic course is normal, and also the internal control standard for the kit.