ZandCell COVID-19 Triple Antibody Test
The ZandCell COVID-19 IgA/IgG/IgM Antibody Test is a rapid test that qualitatively detects severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Using a rapid COVID-19 test provides an opportunity to identify more individuals who are unaware they have been infected. The antibody test of ZandCell is based upon the fact that after infection the body reacts
with the production of very specific antibodies to fight the disease. In the beginning, this will be IgM, and at later stages IgG antibodies. Those antibodies will be found in the peripheral blood. Therefore, the blood sample is collected after a fingerstick. After chromatography, the antibodies will form a complex and can be made visible with coloring techniques.
Sample size: 693
CE-certified for in vitro diagnostic use for symptomatic or asymptomatic individuals.
Instructions for use
Please read the kit instructions carefully before use
1. Open the test sample and unpack the aluminum foil bag, remove the test cassette and place it on a horizontal table
3. Add a drop of blood to the sample well of the test cassette
4. Immediately add 2 drops of sample dilution solution to the sample well
5. Incubate for 2-10 minutes to achieve results (note – reading beyond 30 minutes is invalid)
INTERPRETATION OF RESULTS
The control line is only visible on the test device and the absence of
any burgundy color in both G and M. No anti-Covid antibodies
2. IgM POSITIVE:
The control line (C) and IgM line (IgM) are visible on the test device.
The test indicates the presence of IgM anti-COVID-19 in the
specimen and The result is IgM anti-COVID-19 positive.
3. IgG POSITIVE:
The control line (C) and IgG line (IgG) are visible on the test device.
The test indicates the presence of IgG anti-COVID-19 in the
specimen and The result is IgG anti-COVID-19 positive.
4. IgG and IgM POSITIVE:
The control line (C), IgM (IgM) and IgG (IgG) are visible on the test
device. The test indicates the presence of both IgG and IgM anti-
COVID-19 in the specimen. The result is IgG and IgM anti-COVID-19
The control line fails to appear. Insufficient specimen volume or
incorrect procedural techniques may be the reasons for control line
failure. Repeat the test using a new test device.
We ship with express shipping worldwide
*Note: These kits are only available for sale to companies in the healthcare industry.
For in vitro diagnostic use only. For professional use only. Orders can only be placed by representatives and no consumers. All orders must be confirmed to be valid.
Package insert limited warranty and disclaimer
ZandCell.com makes no and expressly disclaims any representation or warranty, express or implied, regarding this kit or any information, method, process, procedure, chemical, or other material contained in this kit (the “material”), including without limiting the foregoing, any representation or warranty regarding the use of this kit or any results produced from its use, that this kit or any of the material will not infringe any third party rights or that the material is accurate or complete, or that this kit is of merchantable quality or is fit for any particular purpose. ZandCell.com expressly disclaims any and all liability whatsoever for any damages, whether direct, indirect, special, proximate, consequential, or otherwise, including injury to persons or property, death, contamination, and any other adverse consequences, resulting in any way from the use of this kit or any of the material, or from any errors or omissions in the material and any errors or defects in, or failure of, this kit, whether claimed in contract, negligence or any other cause of action. in no event will ZandCell.com’s liability exceed the amount paid for this kit. users are warned that this kit is intended only to be used by, and to supplement the informed judgment of, appropriately qualified medical personnel. users assume sole responsibility for the use of this kit, including all responsibility for determining the appropriateness of its use in any particular situation, for any conclusions drawn from the results of its use, and for any actions taken or not taken as a consequence of the results of this kit.
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