COVID Test Kits Are Now Available
Protect Yourself. Protect Your Team. Protect Your Business.
Beeline Purchasing and STI are proud to assist in the distribution of Rapid Response COVID-19 test kits, both for active infection detection, and current IgG and IgM antibodies.
Rapid COVID-19 Antibody Test
Taken At Home, Shipping IncludedNo appointment needed! Easily administer the test yourself.
Results are provided within 48 hours of receiving your test kit.
Each test provides results regarding the presence of IgG and IgM antibodies.
Avoid long nasal swabs, a simple finger prick provides the sample.
RT-PCR Nasal Swab Test for COVID-19
Taken At Home, Shipping IncludedDetect current exposure to the virus that causes COVID-19.
Nasal Swab only needs to penetrate the nose by one inch and is self-collected.
No appointment needed! Easily administer the test yourself.
Results are provided within 48 hours of receiving your test kit.
Bulk Discounts Available
The EEOC has validated COVID-19 testing for employees returning to work. If you are interested in ordering test kits for your workforce or to have on hand for future preventative testing – contact our team today.
Orders starting at 50+ tests are subject to special pricing. Please call our sales team at 1-800-546-4451.
How It Works:
Order Your Test(s)
Your COVID-19 at home test kit ships quickly to your home or business.
Perform Your Test
Read your kit directions and quickly administer your test (finger prick or nasal swab) in minutes.
Return Your Sample
Use the supplied pre-paid shipment materials to send your sample to our lab.
Get Your Results
Your results will be emailed to you within 48 hours of our lab receiving your sample.
Order Your COVID-19 At-Home Test Kits
Test Kits are shipped directly to your home or business. Once you have administered your test, the lab must receive your results within 9 days to perform the analysis and provide you your results. Results are emailed to you within 48 hours.
*Shipping of tests is included, and each test kit contains a pre-paid return shipping form. Your sample must be received by the lab no later than 9 days after the sample was taken to ensure accurate results.
Our Trusted Lab Partner
Having performed over 51 million tests since 1978, Immuno Labs is a trusted laboratory partner for over 12,000 physicians. Immuno Labs is CAP (College of American Pathologists) proficient and is a federally licensed CLIA lab (Clinical Laboratory Improvement Amendments) in 49 US States (excluding New York). They also hold State Clinical Laboratory Licenses for California, Maryland, Florida, Pennsylvania, and Rhode Island.
Answers to Your Questions
How do I get my results?
Each kit includes pre-paid return mailing materials and directions to discreetly send your sample to our lab. Once we have received your sample, it will be processed and you will be emailed your results within 48 hours.
Will insurance cover my test kits?
FOI Laboratories will process your payment for test kits. You will be provided with an automatic itemized receipt of your order via email from FOI, which can be used for reimbursement from your health insurance provider or health coverage plan. We do not communicate with insurance providers directly.
Isn't free coronavirus testing available?
Yes. However, most free clinics require you to wait publicly in a long line around others who are believed to be sick with COVID-19. This form of testing tests for active infections. The results from these tests are not rapid, and by the time many receive their results, they have either infected others or have already improved from their prior symptoms.
Rapid COVID-19 Antibody Testing
RT-PCR Nasal Swab Test for COVID-19
How is the Rapid Antibody test taken?
Tests can be taken on your own, in the privacy of your home or place of business. Our test uses Serology to test for specific antibodies, this requires a quick finger prick and collection of a blood sample. Collecting a sample typically takes 3-5 minutes.
Will my results reveal an active infection of COVID-19?
Our COVID-19 Antibody testing detects both IgM and IgG antibodies. Our test is qualitative, meaning your report will provide a “Positive” or “Negative” result for each of these antibodies.
What is the finger prick like?
If you have questions about collecting a sample, you can watch our instructional video here.
Does the Rapid Antibody test prove 100% immunity?
If someone has a positive antibody test, they should then also have a molecular test performed to further validate their current COVID-19 status and viral load.
What is the difference between IgG and IgM antibodies?
IgM antibodies are first detectable 3-6 days after being exposed to the virus and are not detectable after 30 days. The highest level of IgM will be detected at 9 days after exposure to the virus.
IgG antibodies are first detectable 4-8 days after being exposed to the virus. The highest level of IgM will be detected at 17 days after exposure to the virus. It is not known how long IgG will be detectable; it is assumed it can be detected for 1-2 years, but current studies have proven detection up to 50 days.
What does the RT-PCR test provide?
The RT-PCR test has the earliest, most accurate detection of whether or not someone has the SARS-COV-2 virus and thus could be contagious to others whether they are symptomatic or not.
Will the RT-PCR test show me when I was infected?
The RT-PCR testing is valuable to detect right now if you have the SARS-CoV-2 virus that causes the COVID-19 disease. The detection window for RT-PCR is 2-3 days after you have been infected and detection continues until 14 days after infection.
How does the RT-PCR test work?
The RT-PCR test is collected via a nasal swab that has to be inserted about 1 inch into the nose, by the user. This is NOT the painful swab that goes deep into the nose. The collection kit and test analysis will be performed by our partner labs upon receiving your sample.
Are there instructions?
To download step-by-step instructions in both English and Spanish for a Nasal Collection Sample, click here.
Are COVID testing and results FDA-approved?
Yes, Immuno Labs is a fully licensed laboratory. They are federally licensed by CLIA; they are CAP Accredited; and they have FDA Emergency Use Authorization for the COVID-19 testing they are performing.
Is this nasal swab testing accurate?
Due to the high demand for COVID-19 testing there has been a lot of innovation and validation to prove new methods of collection. This test is fully comparable to the nasopharyngeal swab, which is the most popular test right now.
Stay Educated on SARS-CoV-2 Antibody Testing
Research continues to bring new information about the symptoms, spread, and testing of the SARS-CoV-2 Virus. Continue to check for updates for the latest information from the US Center for Disease Control, The FBI, and the US Government in regards to Serology Antibody Testing for COVID-19 and RT-PCR Nasal Swab Tests, some of which is included below.
FBI Warns of Potential Fraud in Antibody Testing for COVID-19
The Federal Bureau of Investigation is warning the public about potential fraud schemes related to antibody tests for COVID-19. Scammers are marketing fraudulent and/or unapproved COVID-19 antibody tests, potentially providing false results. In addition, fraudsters are seeking to obtain individuals’ personal information (names, dates of birth, Social Security numbers, etc.) and personal health information, including Medicare and/or private health insurance information, which can be used in future medical insurance or identity theft schemes.
False Positive Results with BD SARS-CoV-2 Reagents for the BD Max System
The U.S. Food and Drug Administration (FDA) is alerting clinical laboratory staff and health care providers of an increased risk of a false positive result with BD SARS-CoV-2 Reagents for the BD Max System test. In one study, the manufacturer found approximately three percent (3%) of results were false positive results. The test is designed to detect viral nucleic acid from the virus that causes COVID-19 in upper respiratory specimens, such as nasal swabs. The test received an Emergency Use Authorization on April 8, 2020.
Serology Testing for COVID-19 at CDC
The CDC test is not currently designed to test individuals who want to know if they have been previously infected with SARS-CoV-2. Commercial tests are available to provide test results to individuals.CDC’s serologic test has been designed and validated for surveillance and research purposes. It is designed to estimate the percentage of the U.S. population previously infected with the virus – information needed to guide the response to the pandemic and protect the public’s health.
CDC Releases Guidelines for Using Antibody Tests for COVID-19
CDC has developed interim guidance for how healthcare providers, laboratories, and public health staff should use antibody tests. These tests look for the presence of antibodies, which are proteins made in response to infections. Antibodies are detected in the blood of people who are tested after infection; they show the body’s efforts to fight off a specific infection. The virus that causes COVID-19 is new, and what we know about it changes rapidly. This guidance will be updated as more information becomes available.
How to Use Your Rapid COVID-19 Antibody At-Home Test Kit
Order Proccessing and Customer Support Performed by FOI Laboratories.
Collection Analysis Performed by Immuno Laboratories, Inc. | CLIA #: 10D0284781