Introduction
BGI’s Real-Time Fluorescent RT-PCR kit for detecting 2019-nCoV(SARS-CoV-2) is a qualitative in vitro nucleic acid amplification assay used to detect SARS-CoV-2 using reverse transcription PCR from a throat swab and Bronchoalveolar Lavage Fluid（BALF） samples. The kit is widely used for rapid detection and outbreak control of COVID-19 in China. BGI is distributing its RT-PCR kits to more than 180 countries and regions around the world. With its high specificity, sensitivity, and rapid response, it can effectively assist the diagnosis of disease and improve the diagnosis efficiency.
Product Features
- NMPA Certified / CE Marked / FDA Authorized / PMDA Approved
- Results issued in 90 minutes
- One Step-Reaction
- High Sensitivity and Specificity
LOD of 100 copies/mL
No cross-reactivity with the human genome and other pathogens including 54 pathogens, such as human coronavirus OC43, 229E, HKU1, and NL63(HCoV-OC43, HCoV-229E, HCoV-HKU1, HCoV-NL63), etc.
Whole-Process Quality Control
Internal control was set to monitor the laboratory procedures including nucleic acid extraction, reverse transcription, and amplification in each reaction.
- Compatible to Universal Real-time PCR system
- Over 1.2 Million Tests kits have been produced
The kits are internationally available and are currently being distributed to more than 50 countries and regions worldwide. Each kit provides reagents sufficient for 50 reactions.
