Qualitative and Quantitative Determination of MERS-CoV S1-Specific Antibodies Using ELISA
Identifieur interne : 002458 ( Ncbi/Merge ); précédent : 002457; suivant : 002459Qualitative and Quantitative Determination of MERS-CoV S1-Specific Antibodies Using ELISA
Auteurs :Source :
- MERS Coronavirus ; 2019.
Abstract
Indirect enzyme-linked immunosorbent assay (ELISA) enables detection and quantification of antigen-specific antibodies in biological samples such as human or animal sera. Most current MERS-CoV serological assays such as neutralization, immunofluorescence, or protein microarray rely on handling of live MERS-CoV in high containment laboratories, highly trained personnel as well as the need for expensive and special equipment and reagents representing a hurdle for most laboratories especially when resources are limited. In this chapter, we describe a validated and optimized indirect ELISA protocol based on recombinant S1 subunit (amino acids 1–725) of MERS-CoV for qualitative and quantitative determination of MERS-CoV-binding antibodies.
Url:
DOI: 10.1007/978-1-0716-0211-9_11
PubMed: 31883093
PubMed Central: 7122216
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<front><div type="abstract" xml:lang="en">Indirect enzyme-linked immunosorbent assay (ELISA) enables detection and quantification of antigen-specific antibodies in biological samples such as human or animal sera. Most current MERS-CoV serological assays such as neutralization, immunofluorescence, or protein microarray rely on handling of live MERS-CoV in high containment laboratories, highly trained personnel as well as the need for expensive and special equipment and reagents representing a hurdle for most laboratories especially when resources are limited. In this chapter, we describe a validated and optimized indirect ELISA protocol based on recombinant S1 subunit (amino acids 1-725) of MERS-CoV for qualitative and quantitative determination of MERS-CoV-binding antibodies.</div>
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