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COVID-19 IgM and IgG Antibody Screening and Viral Testing

Get two 10-minute antibody screenings plus  the Gold Standard viral culture . All 3  for highest accuracy. 

Our Doctor Explains

Luke B. Berry, MD

We offer a 3 step process -  COVID-19 IgM and IgG antibody screenings along with the Gold Standard viral culture test.  The antibody screens determine if you were exposed recently or in the past,  your body's response, and if you have viral particles in your secretions. The screening process requires a single drop of blood from a finger prick; results will be relayed to you in an informative packet giving you a comprehensive picture on your exposure to the COVID-19 virus. You will have your antibody results in 10 minutes! 

As always, check  our Facebook Page and the Centers for Disease and Control and Prevention (CDC) for the latest information.

Test your employeES!

Contact us for Business Rates

• COVID-19 Antibody testing is a great way to ensure your employees remain healthy and can return to a safe work environment.
• With onsite testing, we can come to your business or a site convenient for you.
• All results reviewed by our physician.
• Let's partner and get your workforce back to work safely.

Proud Partner of Livingston Med Lab

Livingston Med Lab is a high complexity laboratory, veteran owned locally based in San Antonio, Texas. Together we are dedicated to fight Covid-19.

Antibody screening and Viral Testing for Private Groups

Why wait 5 days when you can know in 10 minutes

COVID Drive Up Lab is prepared to take care of the community during the evolving pandemic. 

We not only  test for viral particles but we also offer ANTIBODY screening for the public.

• Testing Private Groups Onl
• Results in 10 minutes
• Simple Finger Prick Blood Test
• Drive Thru Screening
• Wait in Car for results 
• Insurance Not Accepted

Our Tests are Proudly Made in the USA!

Read more


Rapid test recipients will also have a confirmatory naso-pharyngeal swab sent off to a lab to confirm results. Considering that serology tests are less complex than molecular tests and are solely used to identify antibodies to the virus, FDA does not intend to object to the development and distribution by commercial manufacturers or development and use by laboratories of serology tests to identify antibodies to SARS-CoV-2, where the test has been validated, notification is provided to FDA, and information along the lines of the following is included in the test reports:
• This test has not been reviewed by the FDA.
• Results from antibody testing should not be used as the sole basis to diagnose or exclude SARS-CoV-2 infection or to inform infection status.
• Negative results do not rule out SARS-CoV-2 infection, as a recent exposure may not elicit an immune response early on (1-3 days). Follow-up testing with a molecular diagnostic should be considered to rule out infection in these individuals.
• Positive results may be due to past or present infections

Business Hours

Monday - Sunday


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