PropertyValue
?:abstract
  • Aim: Coronavirus disease 2019 antibody testing often relies on venous blood collection, which is labor-intensive, inconvenient and expensive compared with finger-stick capillary dried blood spot (DBS) collection. The purpose of our work was to determine if two commercially available anti-severe acute respiratory syndrome coronavirus 2 enzyme-linked immunosorbent assays for IgG antibodies against spike S1 subunit and nucleocapsid proteins could be validated for use with DBS. Materials & methods: Kit supplied reagents were used to extract DBS, and in-house DBS calibrators were included on every run. Results: Positive/negative concordance between DBS and serum was 100/99.3% for the spike S1 subunit assay and 100/98% for the nucleocapsid assay. Conclusion: Validation of the DBS Coronavirus disease 2019 IgG antibody assays demonstrated that serum and DBS can produce equivalent results with minimal kit modifications.
is ?:annotates of
?:creator
?:doi
?:doi
  • 10.4155/bio-2020-0289
?:journal
  • Bioanalysis
?:license
  • cc-by-nc-nd
?:pdf_json_files
  • document_parses/pdf_json/6c6e2a4544e5b5a4f8873dff8cae2fc53261da4a.json
?:pmc_json_files
  • document_parses/pmc_json/PMC7739400.xml.json
?:pmcid
?:pmid
?:pmid
  • 33319585.0
?:publication_isRelatedTo_Disease
?:sha_id
?:source
  • Medline; PMC
?:title
  • Validation of dried blood spot sample modifications to two commercially available COVID-19 IgG antibody immunoassays
?:type
?:year
  • 2020-12-15

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