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enzyme linked immunosorbent 10.1128/JCM.00290-21

In this study, a high-throughput SARS-CoV-2 multiplex microsphere immunoassay (MMIA) was developed for the receptor binding domain (RBD) and nucleocapsid (N) that was more sensitive than enzyme-linked immunosorbent assay (ELISA) (98% versus 87%).

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enzyme linked immunosorbent 10.21203/RS.3.RS-248589/V1

NiV antibodies were detected using enzyme-linked immunosorbent assay or multiplex microsphere immunoassay.

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Multiplex Microsphere Immunoassay 10.1186/s12879-021-06482-0

This acute DENV infection occurred in the presence of a remote ZIKV infection as determined by antibodies to ZIKV NS1 envelope by multiplex microsphere immunoassay and an exceptionally high plaque reduction neutralization titer to ZIKV.

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Multiplex Microsphere Immunoassay 10.1128/JCM.00290-21

In this study, a high-throughput SARS-CoV-2 multiplex microsphere immunoassay (MMIA) was developed for the receptor binding domain (RBD) and nucleocapsid (N) that was more sensitive than enzyme-linked immunosorbent assay (ELISA) (98% versus 87%).

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Fluorescent Microsphere Immunoassay 10.1155/2021/6613162

In USP21fl/flFOXP3Cre mice, levels of IFN-gamma, IL-4, anti-soluble egg antigen (SEA) IgG and anti-soluble worm antigen preparation (SWAP) IgG increased in blood, as determined using ELISAs and multiplex fluorescent microsphere immunoassays, while the levels of IL-10, lL-17A, IL-23, IL-9, and anti-SEA IgM decreased.

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Fluorescent Microsphere Immunoassay 10.1101/2021.06.07.21258375

Serum samples were tested for the presence of antibodies using a fluorescent microsphere immunoassay (FMIA), neutralization of SARS-CoV-2 Spike-pseudotyped particles (SARS-CoV-2pp) assay, and serum virus neutralization (SVN) assay.

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Multiplex Microsphere Immunoassay Fluorescent Microsphere Immunoassay Fluorescence Microsphere Immunoassay Luminex Microsphere Immunoassay Explore More

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Fluorescence Microsphere Immunoassay 10.1016/J.MICROC.2021.106024

A rapid lateral flow fluorescence microsphere immunoassay test strip (FM-ICTS) for the detection of deoxynivalenol (DON) residues in different agricultural products was established based on competitive immunoreactivity.

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Fluorescence Microsphere Immunoassay 10.1016/j.jviromet.2019.04.011

We evaluated a multiplexing fluorescence microsphere immunoassay (FMIA) for the detection of IgG and IgM antibodies in ruminant sera against the RVFV nucleocapsid Np, glycoprotein Gn, and non-structural protein NSs.

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Microsphere Immunoassay sentence examples within Luminex Microsphere Immunoassay

Luminex Microsphere Immunoassay 10.1111/tbed.14219

Serum samples were screened for the presence of anti‐SARS‐CoV‐2 IgG antibodies using a Luminex microsphere immunoassay (MIA).

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Luminex Microsphere Immunoassay 10.1101/2021.03.06.433708

Serum samples were screened for the presence of anti-SARS-CoV-2 IgG antibodies using a Luminex microsphere immunoassay (MIA).

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10.3390/v13071299

All serum samples were tested for IgG antibodies against DENV, CHIKV, ZIKV and MAYV using a recombinant antigen-based microsphere immunoassay with a subset further evaluated through anti-ZIKV microneutralization tests.

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10.1002/vms3.638

In this study, SARS-CoV-2 infection was evaluated in two cats by clinical observation, molecular biology (qPCR and NGS), and serology (microsphere immunoassay and seroneutralization).

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10.1101/2021.03.24.436830

In this report, SARS-CoV-2 infection was evaluated in two cats by clinical observation, molecular biology (qPCR and NGS), and serology (Microsphere immunoassay and seroneutralization).

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Microsphere Immunoassay

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Sep 14, 2024

What is/are Microsphere Immunoassay?

Microsphere Immunoassay - All serum samples were tested for IgG antibodies against DENV, CHIKV, ZIKV and MAYV using a recombinant antigen-based microsphere immunoassay with a subset further evaluated through anti-ZIKV microneutralization tests. ^[1] In this study, SARS-CoV-2 infection was evaluated in two cats by clinical observation, molecular biology (qPCR and NGS), and serology (microsphere immunoassay and seroneutralization). ^[2] In this report, SARS-CoV-2 infection was evaluated in two cats by clinical observation, molecular biology (qPCR and NGS), and serology (Microsphere immunoassay and seroneutralization). ^[3]

enzyme linked immunosorbent

In this study, a high-throughput SARS-CoV-2 multiplex microsphere immunoassay (MMIA) was developed for the receptor binding domain (RBD) and nucleocapsid (N) that was more sensitive than enzyme-linked immunosorbent assay (ELISA) (98% versus 87%). ^[1] NiV antibodies were detected using enzyme-linked immunosorbent assay or multiplex microsphere immunoassay. ^[2] NiV antibodies were detected using enzyme-linked immunosorbent assay or multiplex microsphere immunoassay. ^[3]

Multiplex Microsphere Immunoassay

This acute DENV infection occurred in the presence of a remote ZIKV infection as determined by antibodies to ZIKV NS1 envelope by multiplex microsphere immunoassay and an exceptionally high plaque reduction neutralization titer to ZIKV. ^[1] In this study, a high-throughput SARS-CoV-2 multiplex microsphere immunoassay (MMIA) was developed for the receptor binding domain (RBD) and nucleocapsid (N) that was more sensitive than enzyme-linked immunosorbent assay (ELISA) (98% versus 87%). ^[2] NiV antibodies were detected using enzyme-linked immunosorbent assay or multiplex microsphere immunoassay. ^[3] NiV antibodies were detected using enzyme-linked immunosorbent assay or multiplex microsphere immunoassay. ^[4] Building on this premise, we have previously developed a flavivirus multiplex microsphere immunoassay (MIA) for the serologic diagnosis of ZIKV and DENV infections. ^[5]

Fluorescent Microsphere Immunoassay

In USP21fl/flFOXP3Cre mice, levels of IFN-gamma, IL-4, anti-soluble egg antigen (SEA) IgG and anti-soluble worm antigen preparation (SWAP) IgG increased in blood, as determined using ELISAs and multiplex fluorescent microsphere immunoassays, while the levels of IL-10, lL-17A, IL-23, IL-9, and anti-SEA IgM decreased. ^[1] Serum samples were tested for the presence of antibodies using a fluorescent microsphere immunoassay (FMIA), neutralization of SARS-CoV-2 Spike-pseudotyped particles (SARS-CoV-2pp) assay, and serum virus neutralization (SVN) assay. ^[2] We describe the development and validation of a duplex fluorescent microsphere immunoassay (FMIA) to simultaneously detect and differentiate antibodies to BTV and EHDV in a single bovine serum sample. ^[3] Serum samples were tested for the presence of antibodies using a fluorescent microsphere immunoassay (FMIA), neutralization of SARS‐CoV‐2 spike‐pseudotyped particles (SARS‐CoV‐2pp) assay, and serum virus neutralization (SVN) assay. ^[4]

Fluorescence Microsphere Immunoassay

A rapid lateral flow fluorescence microsphere immunoassay test strip (FM-ICTS) for the detection of deoxynivalenol (DON) residues in different agricultural products was established based on competitive immunoreactivity. ^[1] We evaluated a multiplexing fluorescence microsphere immunoassay (FMIA) for the detection of IgG and IgM antibodies in ruminant sera against the RVFV nucleocapsid Np, glycoprotein Gn, and non-structural protein NSs. ^[2] Previously, we developed an 11‐plex magnetic fluorescence microsphere immunoassay (MAGPIX) by using globular head domain recombinant hemagglutinins (rHAs) with serum adsorption using two ectodomain rHAs. ^[3]

Luminex Microsphere Immunoassay

Serum samples were screened for the presence of anti‐SARS‐CoV‐2 IgG antibodies using a Luminex microsphere immunoassay (MIA). ^[1] Serum samples were screened for the presence of anti-SARS-CoV-2 IgG antibodies using a Luminex microsphere immunoassay (MIA). ^[2]