A panel of ten purified respiratory viruses pooled that have been inactivated to render them non‐infectious and formulated in viral transport medium.
- External quality control for nucleic acids detection
- Validation of the complete analytical process: extraction & amplification
- Complete inactivated microorganism in a matrix
- Quantified controls (low positive)
- 10 single-use lyophilized vials
> Further information available for the design of primers and probes:
· Complete genome:
Adenovirus 4 AY594253.1
Novel influenza A H1N1 FJ966976.1, FJ969531.1, FJ969529.1, FJ969540.1, FJ969536.1,
FJ984386.1, FJ969537.1, FJ969528.1
Parainfluenza 2 AF533012.1
RSV subtype A AY911262.1
RSV subtype B AY353550.1
· Partial sequences:
Coronavirus EF198679.1
Influenza A H3 GQ293082.1, GQ293081.1, KJ609209, KJ609203, KJ609210
Influenza B CY073893.1, CY073894.1, FJ766839.1, KC866602.1, KC866603.1,
KC866605.1
Parainfluenza 3 EU346887.1
Adenovirus 4, Coronavirus, Influenza A H3, Influenza B, Novel influenza A H1N1, Parainfluenza 1, Parainfluenza 2, Parainfluenza 3, RSV (subtype A), RSV (subtype B)
The use of AmpliRun® Total Controls will enable your lab to:
- Enhance the quality of the whole testing process: extraction and amplification.
- Monitor all aspects of sample testing and instrument performance in the long term.
- Monitor variations in laboratory procedures, including batches of assay reagents.
- Validate and verify new assays.
- Obtain reliable and comparable results.
- Train laboratory personnel/ trial purposes.
- Take corrective actions prior assay failure and detect and troubleshoot suspect results.
- Comply with lab accreditation requirements.
Adenovirus 4, Coronavirus, Influenza A H3, Influenza B, Novel influenza A H1N1, Parainfluenza 1, Parainfluenza 2, Parainfluenza 3, RSV (subtype A), RSV (subtype B)
The use of AmpliRun® Total Controls will enable your lab to:
- Enhance the quality of the whole testing process: extraction and amplification.
- Monitor all aspects of sample testing and instrument performance in the long term.
- Monitor variations in laboratory procedures, including batches of assay reagents.
- Validate and verify new assays.
- Obtain reliable and comparable results.
- Train laboratory personnel/ trial purposes.
- Take corrective actions prior assay failure and detect and troubleshoot suspect results.
- Comply with lab accreditation requirements.