FTD Hepatitis E RNA
One tube multiplex for detection AND quantification of hepatitis E virus and internal control
Multiplex real-time PCR for detection of pathogen genes by TaqMan® technology
One tube multiplex PCR:
- Hepatitis E virus
- internal control
The quantitative validation of FTD Hepatitis E RNA was done with extracted nucleic acid from human EDTA plasma with NucliSENS® easyMag® and ABI® 7500.
In clinical performance evaluation studies the test was also successfully qualitatively used with human EDTA blood, serum, stool, ascites and CPDA (citrate phosphate dextrose adenine) blood.
In case EDTA blood, serum, stool, ascites and CPDA (citrate phosphate dextrose adenine) blood are intended to use for quantitative analysis, the procedure has to be validated by the user. Be aware that in stool samples the sensitivity of the test is reduced.
6 months minimum
To find out if the extraction method or qPCR thermocycler available in your facility is compatible with FTD assays, please see our full and detailed compatibility list under the “Resources” area or contact email@example.com
Product availability may vary from country to country and is subject to varying regulatory requirements. Please contact your FTD organization for further details.