AbC-19 rapid antibody test

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AbC-19 rapid antibody test

The AbC-19 rapid antibody test is a diagnostic tool designed to detect the presence of antibodies against the SARS-CoV-2 virus, which causes COVID-19. This test is intended to identify individuals who have been previously infected with the virus and have developed an immune response.

Development and Approval[edit | edit source]

The AbC-19 rapid antibody test was developed by Abingdon Health, a UK-based company specializing in rapid diagnostic tests. The test received regulatory approval from the Medicines and Healthcare products Regulatory Agency (MHRA) in the United Kingdom.

Mechanism[edit | edit source]

The test uses a small blood sample, typically obtained via a finger prick, to detect the presence of IgG antibodies specific to the SARS-CoV-2 virus. The test employs a lateral flow immunoassay technique, similar to that used in pregnancy tests, to provide results within 20 minutes.

Usage[edit | edit source]

The AbC-19 rapid antibody test is primarily used for seroprevalence studies to understand the spread of the virus within a population. It is also used in clinical settings to identify individuals who have developed an immune response following infection or vaccination.

Accuracy[edit | edit source]

Clinical evaluations have shown that the AbC-19 rapid antibody test has a high degree of sensitivity and specificity. Sensitivity refers to the test's ability to correctly identify individuals with antibodies, while specificity refers to its ability to correctly identify those without antibodies.

Advantages[edit | edit source]

  • Rapid results within 20 minutes
  • Easy to administer with minimal training
  • Useful for large-scale seroprevalence studies

Limitations[edit | edit source]

  • Not suitable for diagnosing active COVID-19 infections
  • The presence of antibodies does not necessarily indicate immunity

Related Pages[edit | edit source]

Categories[edit | edit source]

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Contributors: Prab R. Tumpati, MD