Covid-19 Rapid Test Kit, Antibody Tests, Professional Use, box/25

Covid-19 Rapid Test Kit, Antibody Tests, Professional Use, box/25

$650.00 $470.00
(You save $180.00)
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4-6 weeks
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COVID-19 Rapid Test Kit (Box of 25) For Professional Use Only. All Chemical, Biological, Biochemical and other research facilities can order these kits for research and development purposes. All orders are evaluated due to FDA guidelines. If we deem your order as not for professional use, your order will not be processed. We are required to abide by Federally enforced rules.

Availability: In stock. Allow 3-7 days for UPS Ground delivery.

COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) is a solid phase immunochromatographic assay for the rapid, qualitative and differential detection of IgG and IgM antibodies to 2019 Novel Coronavirus in human whole blood, serum or plasma. This test provides only a preliminary test result. Therefore, any reactive specimen with the COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) must be confirmed with alternative testing method(s) and clinical findings.

The COVID-19 IgG/IgM (Whole Blood/Serum/Plasma) Rapid Test Device utilizes lateral flow technology that is used for the qualitative, differential detection of both anti-SARS-CoV-2 IgM and IgG antibodies. In general, antibodies can be detected 1-3 weeks after infection. This test is intended to screen patients
for COVID-19. Combining RNA and Antibody tests can significantly raise the sensitivity for detecting COVID-19 in infected individuals.

  • Available for professional Use or R&D purposes.
  • Time to Results: 10 minutes
  • Specimen: Whole Blood, Serum, Plasma
  • Buffer Included
  • Positive Percent Agreement (PPA): IgG 96.7%; IgM 86.7%; Overall 96.7%
  • Negative Percent Agreement (NPA): IgG 98.0%; IgM 99.0%; Overall 97.0%
  • Non-Refundable, Non-Returnable

Disclosure: The test has not been reviewed by the FDA and 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.

All clinical study reports and data have been completed and are pending FDA Approval.

Box of 25 Includes - 25 Test Cassettes, 25 Droppers, 1 Bottle of Buffer, Product Insert

*One bottle of buffer per box.  (Each test requires 2 drops of buffer.  A bottle of buffer contains 50 drops.)

*Lancets and Alcohol Prep Pads are not included

Instructions for Use:

  1. Remove the test cassette from the sealed foil pouch and use it as soon as possible.
  2. Lay device on flat surface and add specimen (see specific instructions for each specimen type below):
    • For Serum or Plasma Specimen: with the 5 μL plastic dropper provided, draw serum/plasma specimen to exceed the specimen line, as shown in the diagram below. Hold the dropper vertically and transfer drawn serum/plasma specimen into the sample well (S). Immediately add 2 drops (about 80 μL) of sample buffer to the buffer well (B) ensuring that buffer vial tip does not touch the sample. Avoid air bubbles.
    • For Whole Blood Specimen: Hold the 5 μL plastic dropper vertically and transfer 1 drop of whole blood (about 10 μL) to the sample well (S) of the test device. Immediately add 2 drops (about 80 μL) of sample buffer to the buffer well (B) ensuring that buffer vial tip does not touch the sample. Avoid air bubbles.
  3. Wait for the control line (C) to change from blue to a red color. If, after 2 minutes, the sample has not moved across the test window or if blood is still present in the sample well (S), add 1 additional drop of sample buffer to the buffer well (B).
  4. The results should be read in 10 minutes. Do not interpret the result after 15 minutes.


If you develop emergency warning signs for COVID-19 get medical attention immediately. Emergency warning signs include*:

  • Difficulty breathing or shortness of breath
  • Persistent pain or pressure in the chest
  • New confusion or inability to arouse
  • Bluish lips or face

*This list is not all inclusive. Please consult your medical provider for any other symptoms that are severe or concerning.

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