Zika IgG/IgM/NS1 rapid test kit
Product: Zika IgG/IgM Rapid Test kit
Specimen: Whole blood,plasma,serum
Components: Individually packed test devices,Disposable pipettes, Buffer, Package insert
Storage: 2-30 celsius degree
Validity: 24 Months
Zika Virus IgG/IgM Test utilizes the principle of Immuno-chromatography. As the test sample flows through the membrane within the test device, the colored-Zika specific recombinant antigen-colloidal gold conjugate complexes with specific antibodies (IgM and/or IgG) of Zika virus, if present in the sample. This complex moves further on the membrane to the test region where it is captured by the anti-human IgM and/or human IgG antibodies coated on the membrane leading to formation of a colored band, which indicates a positive test results. Absence of this colored band in the test window indicates a negative test result. A built-in control line will always appear in the test window when the test has performed properly, regardless of the presence or absence of anti-Zika virus antibodies in the specimen.
Zika Virus IgG/IgM Test is a rapid immunochromatographic assay for the simultaneous detection of IgG and IgM antibodies to Zika virus in human whole blood, serum or plasma. The assay is used as screening test for zika viral infection.
Step 1 .Add two drop specimen into sample hole.
Step 2.Add one drop buffer into sample hole.
Step 3. Read the result in 10 minutes
1. Negative: ONLY one band in the control line (C). No zikavirus-specific IgG and IgM were detected.
2. IgG Positive: two bands are appeared in the test line (T) and control line (C) in the Zika IgG cassette.
3. IgM Positive: two bands are appeared in the test line (T) and control line (C) in the Zika IgM cassette.
4. IgG and IgM Positive: two bands are appeared in the test line (T) and control line (C). in the both of cassette.
5. Invalid: if at ~10 minutes, the red color band does not appear in the control line (C), even if any shade of a pink-to-red test line (T) appears, the result is considered invalid. If the test is invalid, a new test should be performed with a new patient sample and a new test device.
Winhope Technology Co., Ltd is a worldwide enterprise with R&D, production and trade. It was established in1998.
We are doing international trade with the export of the products manufactured by our factory. The company provides for the clients at home and abroad services of best quality and high efficiency. We sell the products to tens of the countries and areas around the world, and have established good business relationship with many leading brands and multinational corporations.