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Rapid 2019-nCoV IgG/IgM Combo Test

Rapid 2019-nCoV IgG/IgM Combo Test

Key features and details

Designed for the rapid qualitative determination of IgG and IgM antibodies to 2019 novel coronavirus (2019-nCoV, SARS-CoV-2) in human serum, plasma or whole blood.

SKU: 07RDCOV19

Sample Volume:
2 uL
Packaging size:
25 Tests
Ships in one Business Day
Product Description

MP Bio now offers a rapid diagnostic test detecting IgG and IgM antibodies of COVID-19. MP Rapid 2019-nCoVIgG/IgM Combo Test Card is an immunochromatography based one-step in vitro test. It is designed for the rapid qualitative determination of IgG and IgM antibodies to 2019 novel coronavirus (2019-nCoV,SARS-CoV-2) in human serum, plasma, or whole blood. MP Rapid 2019-nCoV IgG/IgM Combo Test Card is a supplementary detection for COVID-19 infected suspected individuals besides nucleic acid testing, which could greatly raise the accuracy of the detection for COVID-19.

  • RAPID AND CONVENIENT: Results in 10 minutes. Requires no instruments.
  • DETECTION OF DIFFERENT CLINICAL STAGES: Infection time can be roughly judges by detecting IgG or IgM.
  • OPTIMIZED DETECTION: Can detect specific antibodies to both N and S virus proteins for improved serological detection rates.
  • SPECIMENS: Easy sampling, only 2 μL of serum, plasma or whole blood is needed.
  • STORAGE: Room temperature, 18 month shelf life.

Usage Statement

This product is CE-IVD marked for professional use and complies with the European In-Vitro Diagnostic Devices Directive (98/79/EC). Not for sale in the USA.

Specifications
SKU 07RDCOV19
Analyte / Target IgG and IgM antibodies to COVID-19
Base Catalog Number RDCOV19
Components Rapid 2019-nCov IgG/IgM Combo Test Card x 25, sample buffer, capillary pipettes and instructions for use.
Disease Screened Coronavirus disease 2019 (COVID-19)
Pack Size 25 Tests
Sample Type Plasma, Serum, Whole Blood
Sample Volume 2 uL
Sensitivity 94.74%
Species Reactivity Human
Specificity 97.06%
Storage Store the kit and it's components at 2 °C - 30 °C.
Usage Statement This product is CE-IVD marked for professional use and complies with the European In-Vitro Diagnostic Devices Directive (98/79/EC). Not for sale in the USA.
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