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Related Concept Videos

Enzyme-Linked Immunosorbent Assay01:33

Enzyme-Linked Immunosorbent Assay

In 1971, Peter Perlman and Eva Engvall developed an Enzyme-linked immunosorbent assay (ELISA or EIA). ELISA differs from western blot in that the assays are conducted in microtiter plates or in vivo rather than on an absorbent membrane.
There are many different types of ELISAs, but they all involve an antibody molecule whose constant region binds an enzyme, leaving the variable region free to bind its specific antigen.  Enzyme-substrate reaction allows the antigen to be visualized or quantified.

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Related Experiment Video

Updated: May 12, 2026

A Protein Microarray Assay for Serological Determination of Antigen-specific Antibody Responses Following Clostridium difficile Infection
09:12

A Protein Microarray Assay for Serological Determination of Antigen-specific Antibody Responses Following Clostridium difficile Infection

Published on: June 15, 2018

Specific serology for emerging human coronaviruses by protein microarray.

C Reusken1, H Mou, G J Godeke

  • 1Centre for Infectious Disease Control, Division Virology, National Institute for Public Health and the Environment, Bilthoven, The Netherlands. chantal.reusken@rivm.nl

Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin
|April 19, 2013
PubMed
Summary
This summary is machine-generated.

A new protein microarray assay detects IgM and IgG antibodies for human coronavirus EMC (hCoV-EMC) and SARS-CoV. This validated method distinguishes between emerging and known coronaviruses using spike protein antigens.

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Area of Science:

  • Immunology
  • Virology
  • Biotechnology

Background:

  • Emerging human coronaviruses (hCoVs) pose significant public health threats.
  • Accurate serological assays are crucial for diagnosing and understanding coronavirus infections.
  • Distinguishing between different hCoV infections, including SARS-CoV and hCoV-EMC, is clinically important.

Purpose of the Study:

  • To develop and validate a specific serological assay for detecting IgM and IgG antibodies against hCoV-EMC and SARS-CoV.
  • To utilize protein microarray technology for sensitive and specific viral antibody detection.
  • To differentiate antibodies against emerging hCoV-EMC from those against SARS-CoV and common hCoVs.

Main Methods:

  • Development of a protein microarray assay employing the S1 receptor-binding subunit of the spike protein of hCoV-EMC and SARS-CoV as antigens.
  • Extensive validation of the assay using serum samples.
  • Testing of sera from patients exposed to common hCoVs to assess cross-reactivity.
  • Testing of sera from convalescent patients infected with hCoV-EMC or SARS-CoV to confirm specificity.

Main Results:

  • The protein microarray assay demonstrated specific detection of IgM and IgG antibodies against hCoV-EMC and SARS-CoV.
  • The assay showed minimal cross-reactivity with sera from individuals exposed to common hCoVs.
  • High specificity was confirmed using convalescent sera from confirmed hCoV-EMC and SARS-CoV infections.

Conclusions:

  • A novel and specific protein microarray assay for detecting hCoV-EMC and SARS-CoV antibodies has been successfully developed.
  • The assay provides a reliable tool for distinguishing between infections caused by emerging and known human coronaviruses.
  • This technology holds promise for improved diagnostics and epidemiological studies of coronavirus outbreaks.