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Development and application of an enzyme immunoassay for coronavirus OC43 antibody in acute respiratory illness
1994
Journal of Clinical Microbiology
Study of coronavirus OC43 infections has been limited because of the lack of sensitive cell culture systems and serologic assays. To improve this circumstance, we developed an indirect enzyme immunoassay (ETA) to detect serum antibody to OC43. Antigen (100 ng) prepared by polyethylene glycol precipitation provided optimal results without a postcoat procedure. Evaluation of intraplate variation indicated that a 22.5-fold increase in serum titer was significant. Sixteen of 18 (89%) paired serum
doi:10.1128/jcm.32.10.2372-2376.1994
fatcat:66vs27cgufb57f4625mtlem4xa