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Kits and products designed to test an individual for the SARS-CoV-2 virus that is known to cause COVID-19; includes rapid tests, reagents, controls, stock, culture fluid, and other products.
Applied Biosystems TaqMan SARS-CoV-2 Control Dilution Buffer is used to dilute the TaqMan SARS-CoV-2 RNA Control (Cat. No. 956118), which is used with the TaqMan SARS-CoV-2 Pooling Assay Kit (Cat. No. A50790).
Fisher Scientific Edge Order by 2 p.m. for same-day shipping. Learn More
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Assess the performance of serological assays for SARS-CoV-2 infections using the Thermo Scientific MAS SARS-CoV-2 Serology Quality Controls. These third-party controls include positive controls for SARS-CoV-2 and a negative control for accuracy.
Nucleic acid test for use on cobas Liat system is the first real-time RT-PCR test authorized for use in screening and testing asymptomatic/symptomatic individuals for SARS-CoV-2 at the point of care, for running a control test/lot validation for the assay
Validate and monitor the performance of molecular diagnostic tests for detecting COVID-19 using the Thermo Scientific™ AcroMetrix™ Coronavirus 2019 (COVID-19) RNA Control (RUO).
Validate and monitor the performance of molecular diagnostic tests for detecting COVID-19 using the Thermo Scientific™ AcroMetrix™ SARS-CoV-2 Control (RUO)
The cobas SARS-CoV-2 & Influenza A/B nucleic acid test is a multiplex real-time polymerase chain reaction (PCR) test that detects and differentiates SARS-CoV-2, Influenza A, and Influenza B. This control kit is for running a control test/lot validation for the assay.
OSOM Flu SARS-CoV-2 Combo Control Kit is intended for use in external quality control with the OSOM Flu SARS-CoV-2 Combo Antigen Test Kit. For Emergency Use Authorization Only.
Used for the qualitative measurement of total antibody (including IgG and IgM) to SARS-CoV-2 in human serum and plasma (K2 EDTA) samples from patients suspected of COVID-19 by a healthcare provider, using VITROS™ ECi/ECiQ/3600 Immunodiagnostic Systems and the VITROS™ 5600/XT 7600 Integrated Systems.