EDI™ Novel Coronavirus COVID-19 ELISA Kits

March 03, 2020

Enzyme Linked Immunosorbent Assays (ELISA) for the qualitative detection of IgM or IgG and the quantitative detection of IgG.

KT-1032

KT-1033

KT-1034

KT-1035

KT-1036

Overview & Statement on the Mutations

The 2019 Novel Coronavirus (COVID-19) is a single-stranded RNA coronavirus. Comparisons of the genetic sequences of this virus have shown similarities to SARS-CoV and other bat coronaviruses. In humans, coronaviruses cause respiratory infections.  Coronaviruses are composed of several proteins including the spike (S), envelope (E), membrane (M), and nucleocapsid (N). It has been suggested that the spike protein has sufficient affinity to the angiotensin converting enzyme 2 (ACE2) receptor to use it as a mechanism of cell entry. Human-to-human transmission of coronaviruses is primarily thought to occur among close contacts via respiratory droplets generated by sneezing and coughing. There are over 90,000 confirmed Coronavirus cases globally with over 3,000 deaths as a direct result of the infection.

Effective detection of the coronavirus is extremely critical. Currently, real-time polymerase chain reaction (RT-PCR) tests detect genetic material to perform coronavirus testing. However, these tests have low rates of specificity and sensitivity and pose risks related to specimen collection and sample handling. Epitope Diagnostics, Inc. has developed a solution to minimize these risks by using IgG and IgM ELISA kits. IgG is the most abundant immunoglobulin to be produced in response to an antigen and is maintained in the body after initial exposure for long term response. IgM is the first immunoglobulin to be produced in response to an antigen and is primarily detected during the early onset of disease.

Serological IgG and IgM test for COVID-19 B.1.1.7 and B.1.351 Lineages

The recent UK SARS-CoV-2 variant called VUI*202012/01 (B.1.1.7 lineage) has accumulated multiple gene mutations in the spike protein. Five are amino acid replacements (D614G, A222V, N439K, Y453F and N501Y), and one deletion (del). The South African variant called 501.V2 (B.1.351 lineage) also has gene mutations in the spike protein: D80A, D215G, E484K, N501Y and A701V. Although the full significance of these mutations is yet to be determined, experts believe that mutations in the receptor spike protein fit the virus invasion to the host.

Do these mutations affect Epitope Diagnostics’ serological IgG and IgM Coronavirus ELISAs (KT-1032, KT-1033 and KT-1034)?

Epitope Diagnostics’ Novel COVID-19 IgG and IgM assays are designed to identify human IgG and IgM reacting to multiple epitopes of SARS-CoV-2 full length Nucleocapsid protein, therefore the mutations in spike protein of the B.1.1.7 and the B.1.351 lineages variants do not impact the safety and effectiveness of Epitope Diagnostics’ COVID-19 IgG and IgM tests.

Epitope Diagnostics’ Proactive Risk Management Plan:
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Epitope Diagnostics informs its distributors and laboratories to analyze and report any suspect test results that do not meet clinical findings. EDI monitors SARS-CoV-2 variants databases in NCBI, GISAID and SARS-CoV-2 publications (PubMed). The information is used to perform thorough bioinformatics analysis quarterly. Based on in silico analysis, the performance of the kit is not impacted by the mutations.
Epitope Diagnostics COVID-19 Product LineupEpitope Diagnostics COVID-19 Product Lineup
Table of expected results for Epitope Diagnostics COVID-19 ProductsTable of expected results for Epitope Diagnostics COVID-19 Products

Technical Specifications

KT-1032 Novel Coronavirus COVID-19 IgG ELISA Kit Informational GraphKT-1032 Novel Coronavirus COVID-19 IgG ELISA Kit Informational Graph
KT-1032 Novel Coronavirus COVID-19 IgG ELISA KitKT-1032 Novel Coronavirus COVID-19 IgG ELISA Kit
KT-1033 Novel Coronavirus COVID-19 IgM ELISA Kit Informational GraphKT-1033 Novel Coronavirus COVID-19 IgM ELISA Kit Informational Graph
KT-1033 Novel Coronavirus COVID-19 IgM ELISA KitKT-1033 Novel Coronavirus COVID-19 IgM ELISA Kit
KT-1034 EDI COVID-19 Nucleocapsid IgG Quantitative ELISA Kit Informational GraphKT-1034 EDI COVID-19 Nucleocapsid IgG Quantitative ELISA Kit Informational Graph
KT-1034 EDI COVID-19 Nucleocapsid IgG Quantitative ELISA KitKT-1034 EDI COVID-19 Nucleocapsid IgG Quantitative ELISA Kit
KT-1035 EDI Quantitative SARC-CoV-2 Spike Protein IgG ELISA Kit Informational GraphKT-1035 EDI Quantitative SARC-CoV-2 Spike Protein IgG ELISA Kit Informational Graph
KT-1036 EDI Quantitative SARC-CoV-2 Neutralizing Antibody ELISA Kit Informational GraphKT-1036 EDI Quantitative SARC-CoV-2 Neutralizing Antibody ELISA Kit Informational Graph

Assay Protocols

Epitope Diagnostics COVID-19 Product Assay ProtocolsEpitope Diagnostics COVID-19 Product Assay Protocols

Instructions for Use

KT-1032 EDI™ Novel Coronavirus COVID-19 IgG ELISA Kit
KT-1033 EDI™ Novel Coronavirus COVID-19 IgM ELISA Kit
KT-1034 EDI™ COVID-19 Nucleocapsid IgG Quantitative ELISA Kit
KT-1035: Quantitative SARS-CoV-2 Spike Protein IgG ELISA
KT-1036: Quantitative SARS-CoV-2 Neutralizing Antibody ELISA

Publications

The following papers utilize the EDI™ Novel Coronavirus COVID-19  IgG or IgM ELISA Kits:

Ahn JY et al. Use of Convalescent Plasma Therapy in Two COVID-19 Patients with Acute Respiratory Distress Syndrome in Korea. J Korean Med Sci. 2020;35(14):e149. Published 2020 Apr 13. doi:10.3346/jkms.2020.35.e149

Ambroise Pare Hospital, Evaluation report of the EDI test at Ambroise Paré Hospital. Assistance Publique Hospitaux de Parix. Published 2020 May 14.

Alexander Krüttgen et al. Comparison of four new commercial serologic assays for determination of SARS-CoV-2 IgG. Journal of Clinical Virology. 2020;128:104394. Published 2020 Apr 22. doi:10.1016/2020.104394

Charlton, C. L., et al. (2020). Evaluation of six commercial mid to high volume antibody and six point of care lateral flow assays for detection of SARS-CoV-2 antibodies. Journal of Clinical Microbiology. doi:10.1128/jcm.01361-20

Christian Bundschuh et al. Evaluation of the EDI enzyme linked immunosorbent assays for the detection of SARS-CoV-2 IgM and IgG antibodies in human plasma. Clinica Chimica Acta. Published 2020 June 8. doi.org/10.1016/j.cca.2020.05.047

Jeffrey D. Whitman, et al. Test performance evaluation of SARS-CoV-2 serological assays. MedRXiv. Published 2020 Apr 29.  doi:10.1101/2020.04.25.20074856 [Not certified by peer review]Margo Egger, et al. Comparison of the Elecsys® Anti-SARS-CoV-2 immunoassay with the EDITM enzyme linked immunosorbent assays for the detection of SARS-CoV-2 antibodies in human plasma. Clinica Chimica Acta. Published 2020 May 28. doi/10.1016/j.cca.2020.05.049

Renata Varnaite, et al. Expansion of SARS-CoV-2-specific Antibody-secreting Cells and Generation of Neutralizing Antibodies in Hospitalized COVID-19 Patients. BioRXiv. Published 2020 May 29. doi/10.1101/2020.05.28.118729
The following article features the EDI™ Novel Coronavirus COVID-19 IgG or IgM ELISA Kits:

Denise Roland. HEALTH Blood of Recovered Covid-19 Patients Is Becoming a Hot Commodity. Wall Street Journal. Published 2020 May 29.

Information for US Customers

At this time, the KT-1032 EDI™ Novel Coronavirus COVID-19 IgG ELISA Kit, KT-1033 EDI™ Novel Coronavirus COVID-19 IgM ELISA Kit, and the KT-1034 EDI™ COVID-19 Nucleocapsid IgG Quantitative ELISA Kit, KT-1035 Quantitative SARS-CoV-2 Spike Protein IgG ELISA kit, KTR-1036 Quantitative SARS-CoV-2 Neutralizing Antibody ELISA kit are available for research use only in the United States. updated 12/4/2020
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It is important to note the following:
  • This test has not been reviewed by the FDA.
  • Negative results do not rule out SARS-CoV-2 infection, particularly in those who have been in contact with the virus.
  • Follow-up testing with a molecular diagnostic should be considered to rule out infection in these individuals.
  • 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.
  • Positive results may be due to past or present infection with non-SARS-CoV-2 coronavirus strains, such as coronavirus HKU1, NL63, OC43, or 229E.

Information for EU Customers

The products are CE-marked. Please refer to the following for our certificate: updated 12/4/2020
CE Certificate

Our facility is ISO 13485:2016 Certified. Please refer to the following for our certificate: updated 12/4/2020
ISO Certificate

Frequently Asked Questions

  1. What type of test is this?
    This is an enzyme linked immunosorbent assay (ELISA) test. It is a serological plate-based assay technique designed for detecting and quantifying substances such as peptides, proteins, antibodies and hormones. This test is not the same as PCR or Rapid Test.
  2. Why not use PCR and Rapid Tests?
    Polymerase Chain Reaction (PCR) is a diagnostic test designed to confirm a clinical disease through the amplification of DNA and RNA. However, PCR can only achieve a sensitivity of 50 to 79%, presents issues during the isolation of the virus from clinical specimen, and requires biosafety level 3 laboratory facilities. Rapid Test Diagnostics (RTD) are lateral-flow assays, that use a dipstick or cassette format to perform a qualitative detection of a disease. However, due to the format of the assay, they can only achieve a sensitivity of 30%. For these reasons, Epitope Diagnostics, Inc. does not offer either of these tests for the detection of COVID-19.
  3. How do I use your tests?
    The kit contains a 96-well ELISA microtiter plate and all the reagents and control materials required to run the test. Each kit can run up to 92 patient samples in singlet, or 46 in duplicate depending on the preference of the laboratory. Tests can be performed manually with any spectrophotometric microplate reader capable of reading absorbance at 450 nm and a ELISA multichannel wash bottle or automatic (semi-automatic) washing system. Assays can be performed on automated instruments with additional validation.
  4. What Biosafety Level should I be using and what guidelines should I be following?
    The Centers for Disease Control and Prevention (CDC) has recommended using BSL-2. Please refer to their guidance Interim Laboratory Biosafety Guidelines for Handling and Processing Specimens Associated with Coronavirus Disease 2019 (COVID-19) for more information.
  5. I am not a healthcare professional, how can I get tested using your kits?
    Epitope Diagnostics, Inc. recommends contacting your healthcare provider directly to request testing with the kits. Please note that we do not perform testing at our facility and cannot disclose which locations are conducting our tests.
  6. How do I place an order for your COVID-19 kits?
    Due to the overwhelming amount of responses, we request that all orders be placed through our customer service in order to ensure traceability. If you are interested in purchasing, please email your appropriate credentials, kit quantity, and forecasting to cs@epitopediagnostics.com. Please note that we are not accepting orders over the phone at this time.
  7. Which automated instruments have your COVID-19 kits been validated on?
    Please refer to the following list of vendors with available protocols:
    Dynex: techservice@dynex.com or 1-800-288-2354.
    Tecan: helpdesk-us@tecan.com or 1- 800-832-2687.

The EDI™ Novel Coronavirus COVID-19 IgG ELISA Kit, EDI™ Novel Coronavirus COVID-19 IgM ELISA Kit, and EDI™ COVID-19 Nucleocapsid IgG Quantitative ELISA Kit are available now!

For more information, contact the Epitope Diagnostics customer service department:
cs@epitopediagnostics.com
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+1 (858) 693-7877