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Vibrant Wellness: Advanced COVID-19 Antibody Screening

What Dr. Jess Loves:

This is a dried blood antigen test for Covid-19 infection. Quantitative antibody assay for four antigens of the COVID-19 virus. The first FDA Emergency Use Authorized test on dried blood spot to test for the presence of COVID-19 antibodies.

The Vibrant COVID-19 Ab assay is a chemiluminescence immunoassay (CLIA) intended for the qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in human serum or Dry Blood Spot (DBS) using fingerstick blood specimen collected by the health care provider.

Markers measured:

  • SARS-CoV-2 Nucleoprotein
  • SARS-CoV-2 Spike Glycoprotein (S1)
  • SARS-CoV-2 Spike Glycoprotein (S2)
  • SARS-CoV-2 Receptor Binding Domain
Dr. Jess created a very special opportunity on her subscription platform where, as a member, you gain access to affordable and convenient lab testing when you need it, no questions asked. No interest financing over 2 months is available on purchases of $400 or more through After Pay during checkout.
Full testing is available in all 50 states.
Only saliva and urine testing are available in Denmark and Spain.
Testing isn’t available in Brazil, Croatia, Russia, Malaysia, Mexico, Sri Lanka, Serbia, Panama, and Peru.
Your results will also explain what these levels may indicate, as well as the next steps you may want to consider. The results of this test do not diagnose a disease or condition, nor do they recommend a specific medication or treatment. It is recommended you share positive results with your health care provider to discuss if additional screening is needed, as it is possible for a false positive test for Lyme disease to occur due to other bacterial infections mistakenly being reported as a positive Lyme antibody test. Also, if your symptoms persist but you tested negative for Lyme disease, you may have tested too soon after you were bitten for your body to have produced enough antibodies to be detectable. Your healthcare provider may recommend testing again if you are symptomatic.

Sample Type: Blood draw

Vibrant testing does not demonstrate absolute positive and negative predictive values for any disease state or condition. Its clinical utility has not been fully established. Vibrant validates the accuracy and precision of the testing but not of its clinical or diagnostic value. So these tests are for wellness and informational purpose only. Vibrant is actively doing clinical research on these samples, de-identified from patients under an IRB and will make research publications towards the same as and when the clinical utility is well established. These tests have been laboratory developed and their performance characteristics determined by Vibrant America LLC, a CLIA-certified laboratory performing the test CLIA#:05D2078809. The test has not been cleared or approved by the U.S. Food and Drug Administration (FDA). Although FDA does not currently clear or approve laboratory-developed tests in the U.S., certification of the laboratory is required under CLIA to ensure the quality and validity of the tests. The general wellness test intended uses relate to sustaining or offering general improvement to functions associated with a general state of health while making reference to diseases or conditions. Content provided for informational purposes only and should not be construed as medical advice. Content provided to help you make a healthy lifestyle, dietary, and treatment choices in consultation with your healthcare provider. It is intended to be used as a tool to encourage a general state of health and well-being. Please consult with your healthcare practitioner for diagnosis and treatment considerations. The Vibrant Wellness platform provides tools for you to track and analyze your general wellness profile.

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