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The V-PLEX SARS-CoV-2 384 Panel 1 (IgG) Kit is a multiplex serology assay that can be used to measure IgG antibodies to three (3) important antigens related to SARS-CoV-2. The three (3) antigens include: SARS-CoV-2 N, SARS-CoV-2 S1 RBD, and SARS-CoV-2 Spike.
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Specifications
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Kit Contents
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Documentation
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References
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Analyte(s)
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SARS-CoV-2 N, SARS-CoV-2 S1 RBD, SARS-CoV-2 Spike
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Species
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Human
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Instrument(s)
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MESO SECTOR S 600
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SECTOR Imager 6000
,
MESO SECTOR S 600MM
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Plate Type
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384-well
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Sample Type
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Serum, Plasma, Saliva, Upper Respiratory Sample
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Usage Statement
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For Research Use Only. Not for use in diagnostic procedures.
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Storage Condition
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Multi-Component
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Schedule B Code
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3822.19.0000
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Product Description
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Storage
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Quantity per Kit
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Serology Control 1.1
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≤-70 °C
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1 vial
(1 mL)
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Serology Control 1.2
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≤-70 °C
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1 vial
(1 mL)
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Serology Control 1.3
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≤-70 °C
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1 vial
(1 mL)
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Reference Standard 1
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≤-70 °C
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1 vial
(1 mL)
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2-8 °C
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2 vial
(5 plate size)
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SARS-CoV-2 384 Plate 1
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2-8 °C
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5 each
(1 each)
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2-8 °C
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2 bottle
(1000 mL)
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RT
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1 bottle
(90 mL)
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RT
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2 bottle
(100 mL)
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MSD Blocker A
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RT
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1 bottle
(250 mL)
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MSD Phosphate Buffer
5X
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RT
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1 bottle
(50 mL)
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Product Description
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Storage
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Quantity per Kit
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Serology Control 1.1
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≤-70 °C
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5 vial
(1 mL)
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Serology Control 1.2
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≤-70 °C
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5 vial
(1 mL)
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Serology Control 1.3
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≤-70 °C
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5 vial
(1 mL)
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Reference Standard 1
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≤-70 °C
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5 vial
(1 mL)
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2-8 °C
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10 vial
(5 plate size)
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SARS-CoV-2 384 Plate 1
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2-8 °C
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25 each
(1 each)
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2-8 °C
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10 bottle
(1000 mL)
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RT
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5 bottle
(90 mL)
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RT
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10 bottle
(100 mL)
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MSD Blocker A
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RT
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5 bottle
(250 mL)
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MSD Phosphate Buffer
5X
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RT
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5 bottle
(50 mL)
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Product Inserts
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Certificate of analysis
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View More
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SDS
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Title
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Journal
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Year
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Diagnostic accuracy of the ultrasensitive S-PLEX SARS-CoV-2 N electrochemiluminescence immunoassay
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IgG Anti-Spike Antibodies and Surrogate Neutralizing Antibody Levels Decline Faster 3 to 10 Months After BNT162b2 Vaccination Than After SARS-CoV-2 Infection in Healthcare Workers
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Immune responses after omicron infection in triple-vaccinated health-care workers with and without previous SARS-CoV-2 infection
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Performance and validation of an adaptable multiplex assay for detection of serologic response to SARS-CoV-2 infection or vaccination
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SARS-CoV-2 Nucleocapsid Plasma Antigen for Diagnosis and Monitoring of COVID-19
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View All
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