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10.3791/62487

http://scihub22266oqcxt.onion/10.3791/62487
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33900295!ä!33900295

suck abstract from ncbi


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pmid33900295      J+Vis+Exp 2021 ; ä (170): ä
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  • A Rapid, Multiplex Dual Reporter IgG and IgM SARS-CoV-2 Neutralization Assay for a Multiplexed Bead-Based Flow Analysis System #MMPMID33900295
  • Angeloni S; Cameron A; Pecora ND; Dunbar S
  • J Vis Exp 2021[Apr]; ä (170): ä PMID33900295show ga
  • The COVID-19 pandemic has underscored the need for rapid high-throughput methods for sensitive and specific serological detection of infection with novel pathogens, such as SARS-CoV-2. Multiplex serological testing can be particularly useful because it can simultaneously analyze antibodies to multiple antigens that optimizes pathogen coverage, and controls for variability in the organism and the individual host response. Here we describe a SARS-CoV-2 IgG 3-plex fluorescent microsphere-based assay that can detect both IgM and IgG antibodies to three major SARS-CoV-2 antigens-the spike (S) protein, spike angiotensin-converting enzyme-2 (ACE2) receptor-binding domain (RBD), and nucleocapsid (Nc). The assay was shown to have comparable performance to a SARS-CoV-2 reference assay for IgG in serum obtained at >/=21 days from symptom onset but had higher sensitivity with samples collected at
  • |Antibodies, Neutralizing/*blood[MESH]
  • |Antibodies, Viral/blood/immunology[MESH]
  • |COVID-19 Serological Testing/*methods[MESH]
  • |COVID-19/blood/*diagnosis/immunology[MESH]
  • |Flow Cytometry/*methods[MESH]
  • |Humans[MESH]
  • |Immunoglobulin G/*blood[MESH]
  • |Immunoglobulin M/*blood[MESH]
  • |SARS-CoV-2/*immunology[MESH]


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