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Lyme Disease IgM/IgG Antibody Detection Kit (Immunochromatography)

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Category:Infectious Diseases

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Lyme Disease IgM/IgG Antibody Detection Kit (Immunochromatography)

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Introduction

[Product Name]

Lyme Disease IgM/IgG Antibody Detection Kit(Immunochromatography)

[Packaging Size]

5 test/kit, 20 tests/kit

[Intended Use]

This kit is used for the qualitative detection of Lyme disease antibodies in vitro as an auxiliary diagnosis of Lyme disease infection.
Lyme disease (Lyme disease) is a zoonotic disease mainly caused by various genotypes of Borrelia burgdorferi (Bb) transmitted by hard ticks, causing multiple system and organ damage in humans and animals [1]. Human infection mainly causes clinical symptoms such as chronic erythema migrans, Lyme disease encephalitis, arthritis, chronic limb dermatitis and myocarditis [2]. Late infection can cause motor dysfunction and even death. This reagent adopts the principle of capture method and immunochromatography to qualitatively detect Lyme disease IgM/IgG antibodies in human whole blood (venous whole blood, fingertip whole blood), serum or plasma samples. It can be used for the auxiliary diagnosis of early Lyme disease infection. This reagent is for in vitro diagnostic use only.

This kit is suitable for Lyme disease antibody detection in patients with certain symptoms.

[Test Principles]

The Lyme disease IgM/IgG antibody detection kit uses the specific antigen of Lyme disease for tracer labeling and use anti-human IgM and anti-human IgG monoclonal antibodies to coat as the detection line. During detection, if there is a certain concentration of Lyme disease antibody (IgM/IgG) in the sample to be tested, the antibody to be tested binds to the specific antigen of Lyme disease virus labeled by the tracer to form a complex, and under the action of chromatography , the complex moves towards the detection line, and is captured by the coated antibody, resulting in a red band. When the sample to be tested does not contain Lyme disease antibodies, the antibody-antigen labeling complex will not be formed, nor will it be captured by the detection line to produce a red band. Regardless of whether the sample contains the antibody to be tested or not, a red band should appear at the quality control line(C line), as the internal control for whether the chromatography process is normal and whether the reagent is invalid.

[Storage Conditions and Shelf-life]

Storage Conditions: 4-30°C, protected from light.
Shelf-life: 12 months tentatively.
See label for production and expiry dates.
The test cassette should be used within 60 minutes after being taken out of the aluminum foil bag.

[ Requirements for Samples]

1. The test samples are human serum, plasma, venous whole blood and fingertip whole blood, including blood samples containing clinical anticoagulants (EDTA, heparin, citrate).
2. Samples should be collected according to conventional standard methods.

3. The collected fingertip whole blood should be used immediately. Serum, plasma and venous whole blood samples should be freshly collected or kept at 2-8°C for no more than 5 days after collection.

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