Ezplex SARS-CoV-2 G Kit
US FDA Emergency Use Authorization (EUA)
For in vitro diagnostics use only.
For prescription use only.
The Ezplex SARS-CoV-2 G kit is a Real-Time PCR in vitro diagnostic test intended for the qualitative detection of nucleic acid from SARS-CoV-2 (RdRp and N genes) in individuals suspected of COVID-19 by their healthcare provider (nasopharyngeal and oropharyngeal swabs and sputum). The test can be quickly and accurately completed through PCR with extracted RNA, and the results can be conveniently viewed using Genetree Viewer assay software.
Compatible with most RT-PCR analyzers
Shelf life of 12 months at -20°C with opened/unopened status.
FDA Emergency Use Authorization (EUA)
Features and Benefits
Fast Results-Produces test results with 2.5 hours post-extraction.
Real-Time PCT- Detection and identification of target genes (RdRP, N) specific for COVID-19 in a single tube.
Specimen Pooling Capability-Five times as many tests can be conducted within the same time period. (FDA EUA and CE IVD).
Sensitivity-Reference material was repeatedly tested through serial dilution to show high analytical sensitivity. FDA SAR-CoV-2 Reference Panel detection limit of 1200 NDU/mL.
Accessibility- Test results can be easily analyzed with dedicated user-friendly Genetree Viewer software.
Targets-COVID-19 (N gene) and COVID-19 (RdRp gene)
Cookies are small text files that can be used by websites to make a user's experience more efficient. The law states that we can store cookies on your device if they are strictly necessary for the operation of this site. For all other types of cookies we need your permission. This site uses different types of cookies. Some cookies are placed by third party services that appear on our pages.
Marketing cookies are used to track visitors across websites. The intention is to display ads that are relevant and engaging for the individual user and thereby more valuable for publishers and third party advertisers.