COVID-19 IgM and IgG antibody Rapid Test
Over 6 million tests currently available
Over 6 million currently available
When Speed and Precision are Essential
Our lateral flow immuno-assays rapid test provides a much easier and faster way to determine previous exposure to the virus that causes COVID-19. Unlike other antibody tests, our test does not require extensive laboratory operations and can be performed on site, under the supervision of a health care professional, consistent with the terms of our FDA Authorization for these tests (download FDA EUA letter of authorization here) .
Orders under 100,000 shipped next day from either our Pennsylvania or Nevada facilities.
Our organization strictly adheres to FDA policies and regulations covering the sale of diagnostic testing supplies for COVID-19. While personal protective equipment (PPE) may be purchased without restriction, our FDA EUA authorization indicates that these tests are intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. Emergency use of this test is limited to authorized laboratories.
Always verify FDA Authorization Status Before Purchasing COVID-19 Testing Supplies. You may verify the current status of our products (and any other manufacturer’s products on the FDA website: FDA Listing for In Vitro Diagnostics EUA’s)
News and Research Updates
Main Mechanism of Antigen into Blood When SARS-CoV-2 invades the lung cells, it will express a large amount of self protein to reassemble the virus particles, causing cell damage and forming inflammation. The virus protein expressed in excess and the virus protein...
Beware Fake Covid Tests: How to tell the good from the ugly... As the world struggles to find the best way to deal with Covid-19, experts agree on one thing: the importance of good testing. Knowing if you have the virus or have had it, recovered and are carrying...
BioHit Healthcare's Rapid Antibody Test Granted EUA It’s official. Biohit’s Sars-CoV-2 IgM/IgG antibody test kit has just been authorized by FDA under a EUA (Emergency Use Authorization) for use in laboratories certified by CLIA (Clinical Laboratory Improvement...
Reinvigorating Society, One Test at a Time
In addition, RDTs help to prevent the spread of COVID-19 through early detection and highly sensitive and specific testing. Because of this, RDTs are ultimately able to decrease the uncertainty surrounding the lack of reliable testing, as well as the likelihood of a “false positive”.
How The COVID-19 Antibody Rapid Test Works
The One-Step SARS-CoV2 (COVID-19) IgG and IgM Antibody Rapid Test is a lateral flow immunochromatographic assay. This means that the test is easy to administer and does not require a lab, and can provide a positive, negative, or invalid result in a matter of minutes.
The test works by washing a sample of blood or serum (liquid part of blood) over a nitrocellulose strip that the antibodies can bind to. If the IgM and/or IgG antibodies are present, a burgundy-colored band(s) will appear. A colored line appearing in the control region (C) is an internal procedural control and confirms sufficient specimen volume as well as correct procedural technique. Absence of a colored band in the test region indicates a negative test result, while a complete absence of bands in the control line indicates that the test is invalid. For more detailed information, visit our FAQs.
Interpretation of Results:
POSITIVE: A test is positive when the control line and at least one test line appear on the test screen. The appearance of T1 test line indicates the presence of COVID-19 specific IgM antibodies, while the appearance of T2 test line indicates the presence of COVID-19 specific IgG antibodies. If both T1 and T2 lines appear, it indicates the presence of both COVID-19 specific IgG and IgM antibodies. The lower the antibody concentration is, the weaker the result line is*.
*The intensity of the color in the test line regions may vary depending on the concentration of SARSCoV-2 antibodies present in the specimen. Therefore, any shade of color in the test line region should be considered positive.
NEGATIVE: A test is negative if one colored line appears in the control region, while no apparent colored line(s) appear in the test line region.
INVALID: A test is considered invalid when the control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. If this happens, review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.
QUALITY CONTROL: A colored line appearing in the control region (C) is an internal procedural control. It confirms sufficient specimen volume and correct procedural technique.
We have been using Avriogenetics biohit Covid 19 rapid antibody test for a few months. We have found it to be accurate, sensitive and specific. This test can be used to assess IGM and IGG status on suspected patients. It can be used to assess recent exposure and allows rapid screening in a cost effective manner. This is not a replacement or in lieu of the PCR test. PCR testing has its place in the testing suspected Covid 19 patients. With this rapid test we have been able to screen large populations and we are very happy with the test. Sam Najmabadi M.D.
Accurate, Reliable COVID-19 Testing at Scale is Within Reach
Flexible order volumes and shipping terms available.