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ABSTRACT: Background
The coronavirus, SARS-CoV-2, is the causative agent for COVID-19, first registered in Wuhan, China and responsible for more than 6 million deaths worldwide. Currently, RT-PCR is the gold-standard method for diagnosing COVID-19. However, serological tests are needed for screening acute disease diagnosis and screening large populations during the COVID-19 outbreak.Objectives
Herein, we described the development and validation of an in-house enzyme-linked immunosorbent assay (ELISA) for detecting the levels of anti-spike-1-RBD IgM antibody (CovIgM-ELISA) in well-defined serum/plasma panel for screening and identifying subjects infected with SARS-CoV-2 in a Latin population.Method
In-house CovIgM-ELISA has the format of an indirect ELISA. It was optimized by
SUBMITTER: Espino AM
PROVIDER: S-EPMC11475847 | biostudies-literature | 2024 Oct
REPOSITORIES: biostudies-literature