0
AMPLIRUN® Total Respiratory Viral Panel Control (Swab), 10 x 200 µL
Catalog No :
CAS Number :
Brand :
In Stock
Specifications:
| Application | molecular biology, Quality Control | ||
| Storage Temperature | -20°C | ||
| Product Type | Nucleic acid controls | Forms | Lyophilized |
| Product Brand | VIRCELL | ||
| Product Grade | Molecular Biology | ||
The Vircell AMPLIRUN® Total Respiratory Viral Panel Control is an external quality control panel designed for nucleic acid detection of ten common respiratory viruses. This panel contains inactivated viruses formulated in a swab transport medium to mimic clinical respiratory specimens, ensuring non-infectious, safe, and reliable use across molecular diagnostic platforms.
By incorporating complete viral genomes, this control validates both nucleic acid extraction and amplification, enhancing reproducibility and compliance with laboratory accreditation standards.
Available Control
| Product Reference | Description | Volume | Nº Vials | Class |
|---|---|---|---|---|
| MBTC020 | AMPLIRUN® Total Respiratory Viral Panel Control (Swab) | 200 µL | 10 single-use vials | CE |
Panel Composition
- Adenovirus 4
- Coronavirus
- Influenza A H3
- Influenza B
- Novel Influenza A H1N1
- Parainfluenza 1
- Parainfluenza 2
- Parainfluenza 3
- Respiratory Syncytial Virus (RSV) subtype A
- Respiratory Syncytial Virus (RSV) subtype B
Key Features
- Complete inactivated microorganisms – includes ten respiratory viruses.
- External quality control – verifies both extraction and amplification steps.
- Respiratory swab matrix – mimics real clinical samples for realistic assay validation.
- Quantified controls – ensures consistent and reproducible results.
- Non-infectious & lyophilized – safe, stable, and reduces transportation costs.
- Single-use vials – 10 lyophilized vials for ease of handling.
- Sequencing data available – supports probe and primer design.
Applications
- External quality control for respiratory viral molecular testing.
- Validation and verification of laboratory-developed and commercial PCR/qPCR assays.
- Long-term monitoring of extraction and amplification processes.
- Reagent and batch-to-batch performance verification.
- Training and competency assessment for laboratory staff.
- Troubleshooting assay failures or suspect results.
- Compliance with laboratory accreditation and regulatory requirements.
Product Details
| Property | Value |
|---|---|
| Volume per vial | 200 µL |
| Nº Vials | 10 single-use lyophilized vials |
| Format | Inactivated whole microorganisms in transport medium |
| Infectivity | Non-infectious |
| Class | CE |
| Pathogens | Adenovirus 4, Coronavirus, Influenza A H3, Influenza B, Novel Influenza A H1N1, Parainfluenza 1, Parainfluenza 2, Parainfluenza 3, RSV subtype A, RSV subtype B |
Sequence data | Influenza A H3 Influenza B Novel Influenza A H1N1 Parainfluenza 3 Parainfluenza 1 Parainfluenza 2 RSV subtype A: PP922776 Adenovirus 4 AY594253.1 Coronavirus: PP810610 RSV subtype B PP034516
|
| Storage | Stable at ambient temperature until reconstituted |
The AMPLIRUN® Total Respiratory Viral Panel Control provides laboratories with a comprehensive, standardized external quality control for molecular detection of ten clinically relevant respiratory viruses. With inactivated microorganisms formulated in a respiratory swab matrix, quantified genomes, and lyophilized stability, this panel is an essential tool for assay validation, quality assurance, and compliance with accreditation standards in clinical virology and molecular diagnostics.