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
Coronavirus: PP810610
RSV subtype B PP034516
· Partial sequences:
Influenza A H3 PP815005, PP815006, PP815007, PP815008, PP815009, PP815010, PP815011, PP815012
Influenza B PP815638, PP815639, PP815640, PP815641, PP815642, PP815643, PP815644, PP815645
Novel Influenza A H1N1: OR565313, OR565314, OR565315, OR565316, OR565317, OR565318, OR565319, OR565320, OR565321
Parainfluenza 3: PP101994
Parainfluenza 1: OR571883
Parainfluenza 2: PP101995
RSV subtype A: PP922776
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.