SureFast® Hepatitis A PLUS
Art. No. F7125
Product info
Intended use
The test is a real-time RT-PCR for the direct and qualitative detection of hepatitis A virus. The test contains an Internal Control RNA (ICR) as an internal control of sample preparation procedure and to determine possible PCR-inhibition.
For RNA-preparation the use of SureFast® PREP DNA/RNA Virus is recommended.
General Information
The real-time PCR assay can be used with established real-time PCR instruments, equipped for detection of two fluorescence emissions at 522 nm and 553 nm (FAM and VIC) at the same time (Rotor-Gene Q, Stratagene Agilent MxSeries, Roche LightCycler® 480/2.0*/1.5* etc.).
Accessories
Dear customers,
we now provide the documents for our products in an electronic format which include the Instructions for Use (IFU), Safety Data Sheets (SDS), Application notes and the Certificate of Analysis (CoA). For batches placed on the market after 1st of January 2024, you can find our documents on the eIFU portal congen.de/information.
| Specifications | |
|---|---|
| Art. No | F7125 |
| Test format | 100 reactions |
| LOD (Detection Limit) | The SureFast® VIRUS Hepatitis A PLUS real-time RT-PCR has a limit of detection of ≤ 50 RNA copies. The assay limit of detection depends on RNA preparation and RNA content. |
| Files | |
|---|---|
| Instructions | German/English |
| MSDS | Statement-MSDS-12-22-NG.pdf (English) |
