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Analysis of COVID-19 convalescent plasma for SARS-CoV-2 IgG using two commercial immunoassays
Coronavirus Disease 2019 (COVID-19) convalescent plasma (CCP) was approved by the FDA for use in severe cases of COVID-19 under an emergency Investigational New Drug (IND) protocol. Eligibility criteria for CCP donors includes documentation of evidence of COVID-19 either by viral RNA detection at th...
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| Vydáno v: | J Immunol Methods |
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| Hlavní autoři: | , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Elsevier B.V.
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7438987/ https://ncbi.nlm.nih.gov/pubmed/32828791 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jim.2020.112837 |
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