Coronavirus Antibody Test

[COVID-19 IgG/IgM Antibody Test]

Slow The Spread

Find out if you may have been infected by COVID-19.

The antibody test used by ARCpoint Labs (COVID-19 IgG/IgM) is a blood test that is designed to detect immune proteins called antibodies, which may indicate that your body has been exposed to COVID-19 (also known as coronavirus or SARS-CoV-2).

ARCpoint Labs uses a network of trusted third-party high complexity lab partners to conduct these antibody tests.

LEARN MORE COVID-19 FAQs

What is a COVID-19 antibody test?

This test is designed to detect the body’s immune response to the infections caused by the SARS-Co-V-2 virus.

NEGATIVE:

The test did not detect the presence of antibodies.

POSITIVE:

You have antibodies that likely resulted from a previous infection with SARS-CoV-2, or possibly a related coronavirus.

For more information, visit the CDC website.

Should I be Tested?

If you believe you have been exposed to COVID-19 or have had symptoms in the past, you may be a good candidate for this test. You must be asymptomatic (free of symptoms) for at least seven (7) days prior to testing.

Testing is Simple And Quick

Step 1

Schedule your appointment

Step 2

Come to your ARCpoint Labs and get your sample collected

Step 3

Get results via a secure email in 3-4 business days*

For more information about testing, fill out the form below and we’ll connect you with your local ARCpoint industry expert.

Contact Information

First Name *

Last Name *

Email *

Zip Code *

What COVID-19 Antibody Testing solutions are you interested in?

Testing for me and my family

Testing for my employees

Are you interested in COVID-19 Viral Testing?

Yes I am interested in Viral Testing

* Important Information

Please note that our tests have not been FDA cleared or approved, but they have been authorized by FDA under Emergency Use Authorizations (EUA’s) for use by authorized laboratories. Depending on the specific test type, these tests are authorized for the detection of SARS CoV-2, its proteins and/or its antibodies. These tests are only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.

Please click below to see the specific FDA disclaimers and additional manufacturer information for each test and device used by ARCpoint or our laboratory partners.

COVID Testing Disclaimers