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AMPLIRUN® Total CMV Control (Plasma), 10 x 200 µL
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Specifications:
| Application | Quality Control | ||
| Storage Temperature | -20°C | ||
| Product Type | Nucleic acid controls | Forms | Lyophilized |
| Product Brand | VIRCELL | ||
| Product Grade | Molecular Biology | ||
The Vircell AMPLIRUN® Total Cytomegalovirus (CMV) Control is an external quality control designed for nucleic acid detection of Cytomegalovirus. This panel contains inactivated CMV formulated in human plasma, providing a clinically relevant sample matrix that mimics real diagnostic specimens.
As a complete, quantified, and non-infectious control, it validates the entire molecular workflow — from nucleic acid extraction to amplification — ensuring reliability and reproducibility in CMV testing.
Available Control
| Product Reference | Description | Volume | Nº Vials | Class |
|---|---|---|---|---|
| MBTC018-R | AMPLIRUN® Total CMV Control (Plasma) | 200 µL | 10 single-use vials | RUO |
Key Features
- Complete inactivated microorganism – CMV formulated in human plasma matrix.
- External quality control – verifies both nucleic acid extraction and amplification.
- Quantified low-positive controls – supports reliable sensitivity testing.
- Plasma formulation – mimics real clinical diagnostic specimens.
- Non-infectious & lyophilized – safe, stable, and eliminates cold-chain shipping requirements.
- Sequencing data available – facilitates probe and primer design.
- Single-use format – 10 lyophilized vials for ease of use and reproducibility.
Applications
- Quality control for CMV molecular diagnostics (PCR/qPCR).
- Validation and verification of in-house and commercial CMV assays.
- Sensitivity, specificity, LoD, and reproducibility testing.
- Long-term monitoring of extraction and amplification workflows.
- Training and competency evaluation for laboratory personnel.
- Troubleshooting assay inconsistencies.
- Supporting compliance with accreditation and regulatory requirements.
Product Details
| Property | Value |
|---|---|
| Volume per vial | 200 µL |
| Nº Vials | 10 single-use lyophilized vials |
| Format | Inactivated CMV in plasma |
| Infectivity | Non-infectious |
| Class | RUO – Research Use Only |
| Sequencing Data | Cytomegalovirus genome |
| Storage | Stable at ambient temperature until reconstituted |
The AMPLIRUN® Total CMV Control provides laboratories with a reliable, standardized external control for validating the complete molecular workflow in cytomegalovirus testing. With a plasma-based matrix, quantified genome copies, and a safe lyophilized format, this control is an essential tool for assay validation, diagnostic accuracy, and quality assurance in clinical virology and molecular diagnostics.