Human Monkeypox Virus Antibody Rapid Test Kits Blood Detection For Mpox IgG/IgM

Monkeypox Virus IgG/IgM Rapid Test Kit Manual

Rapid Test Introduction

Monkeypox virus is an orthopoxvirus, causing a zoonotic disease of monkeypox and a smallpox-like disease in human. The number of human monkeypox cases has been increasing since the 1970s, with the most dramatic increases occurring in the Democratic Republic of the Congo.  Import- and travel-related appearance of outbreaks beyond Africa highlights the global relevance of the disease. The cessation of smallpox vaccination may be just causing the disease to resurge. Detection of monkeypox cases is essential tool for understanding this resurging disease and clinical diagnosis of the disease.

The Monkeypox Virus IgM/IgG Antibody Rapid Test Kit is used for the qualitative detection of Monkeypox Virus IgM/IgG antibody in human serum, plasma or whole blood sample. It is intended for in vitro diagnostic use, and for professional use only.

Rapid Test Contents

• Rapid test cassette with desiccant

• Buffer

• Disposable pipettes

• Package insert

Rapid Test Features

1. Fast check Mpox Virus IgG/IgM antibodies in 15 mins.

2. Easy to use

3. High Accuracy

4. No need laboratory equipment or trainees

Rapid Test Operation

Bring tests, specimens, buffer and/or controls to room temperature (15- 30°C) before use.

1. Remove the test from its sealed pouch, and place it on a clean, level surface. Label the test with patient or control identification. For best results, the assay should be performed within one hour.

2. Transfer 1 drop of whole blood, serum or plasma specimen to the specimen well (S) of the device with the provided disposable pipette, then add 1 drops of buffer and start the timer.

3. Wait for colored line(s) to appear. Interpret the test results in 15 minutes.

Rapid Test Limitations

1. The positive results of this cassette cannot exclude theinfectionofother pathogens other than monkeypox virus.

2. This cassette can only qualitatively detect monkeypoxvirusantibodies in the specimen, and cannot indicate the content oftheantibody in the specimen.

3. This cassette is only used for preliminary screening. If it isnecessary to confirm the diagnosis, clinical symptoms or furtherlaboratory tests should be performed.

For further operation or performance details, please refer to final instruction manual.