The InviScreen® SARS-CoV-2 RT-LAMP kit is an in vitro diagnostic test that uses RT-LAMP technology for the qualitative detection of two specific regions of SARS-CoV-2 RNA in specimens collected from the upper respiratory tract (nasopharyngeal and oropharyngeal swabs). This kit should be used as a screening method for individuals with and without suspicion of COVID-19 disease, and as an alternative to the reference method for diagnosis of COVID-19 (real-time RT-PCR). The test is particularly suitable for detecting SARS-CoV-2 in people who are in the infectious phase. The RT-LAMP reaction takes between 30-40 minutes, depending on the chosen analysis method (fluorescence or colorimetry). This test is indicated to be performed using native samples (without prior RNA extraction) or extracted RNA. Sample collection must be performed by qualified healthcare professionals, and the kit must be used by properly trained healthcare.
Specifications | |
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Sample preparation |
Compatible with native samples without RNA extraction Optional: for RNA extraction the use of RTP® Pathogen Kit (Art. No. 1050100300) or InviSorb® Spin Universal Kit (Art. No. 1040500300) is recommended |
LOD (Detection Limit) | 10 copies/μL |
Specificity | SARS-CoV-2 (Nsp3 and N genes) |
No. of tests | 100 |
Technology | RT-LAMP |
Instrument compatibility | Applied Biosystems™ 7500, Agilent AriaMx™, Bio Rad CFX96 Touch™ and CFX96 Touch™ Deep Well |
Dyes | Channels Target: FAM/SYBR Green |
Certification | CE-IVD (in compliance with EU Directive 98/79/EC on in vitro medical devices) |
Product Name | Package Size | Catalogue No. |
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InviScreen® SARS-CoV-2 RT-LAMP | 100 reactions | 6010003200 |