Antibody Test for COVID
Results in 10 Minutes

For businesses, organizations, nursing homes, small clinics, schools, and more.

Why is Antibody Testing for COVID Important?

Our antibody test for COVID determines if someone was previously exposed to the virus or has had a past infection. For organizations large and small, regularly monitoring this status for individuals provides the science-based knowledge necessary to make informed decisions.
On-site results are ready in 10 minutes. 

Quick Overview

  • On-site testing; no lab analysis necessary
  • Small blood-sample collection required
  • Accurate results in 10 minutes
  • For U.S and International organizations

About the Product

  • Measures IgG and IgM antibodies to determine if participant has had a past COVID infection
  • FDA-authorized under EUA/CE-certified lateral-flow cartridge test
  • Complete instructions and testing materials included

Quick Overview

  • On-site testing; no lab analysis necessary
  • Small blood-sample collection required
  • Accurate results in 10 minutes
  • For U.S and International organizations

About the Product

  • Measures IgG and IgM antibodies to determine if participant has had a past COVID infection
  • FDA-authorized under EUA/CE-certified lateral-flow cartridge test
  • Complete instructions and testing materials included

How it Works

The antibody test uses a small amount of blood dropped into a lateral-flow cartridge to determine if the participant has had a past COVID infection.

Step 1: Draw small amount of blood from test participant

Step 2: Add 1 drop whole blood

Step 3: Add 2 drops of buffer

Step 4: Wait 10 minutes, and then read results

Important Information

  • This test does not determine if a person is currently infected with COVID
  • This test is for organizations large and small in the U.S.A and International

Fill out the form on this page to provide some preliminary information, and one of our COVID experts will follow up with you as soon as possible. 

This test has not been FDA cleared or approved; the test is authorized by FDA under an Emergency Use Authorization (EUA) for use by laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) of 1988, 42 U.S.C. §263a, that meet the requirements to perform high complexity tests. 

Reach Us

Have questions or need assistance? Contact our team.

DNA Technology Park
1 DDC Way
Fairfield, OH 45014

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