AMPLIRUN® Total ZIKV/DENV/CHIKV Control (Plasma), 10 x 200 µL

The Vircell AMPLIRUN® Total ZIKV/DENV/CHIKV Control is an external quality control panel designed for nucleic acid detection of Zika virus, Dengue virus (serotypes 1–4), and Chikungunya virus. This panel consists of six inactivated arboviruses formulated in human plasma to render them non-infectious, enabling safe use across a wide range of molecular diagnostic workflows.

By incorporating the complete microorganism in a clinically relevant matrix, this panel provides robust verification of both nucleic acid extraction and amplification, ensuring reliability and reproducibility in arbovirus diagnostics.

Available Control

Key Features

• Complete inactivated microorganisms – Zika virus, Dengue virus (1–4), and Chikungunya virus formulated in human plasma.
• External quality control – designed to validate the entire analytical workflow, from extraction to amplification.
• Quantified controls – ensure reliable assay calibration and reproducibility.
• Non-infectious & lyophilized – safe, stable, and eliminates cold chain transport costs.
• Sequencing data available – supports probe and primer design.
• Single-use vials – 10 lyophilized vials per kit, ready for reconstitution.

Applications

• Validation and verification of arbovirus nucleic acid extraction and amplification.
• Long-term monitoring of sample preparation and assay performance.
• Quality assurance in diagnostic laboratories handling Zika, Dengue, and Chikungunya testing.
• Reagent and batch performance verification.
• Training and competency assessment of laboratory personnel.
• Troubleshooting suspect results and implementing corrective actions.
• Compliance with laboratory accreditation and regulatory standards.

Product Details

The AMPLIRUN® Total ZIKV/DENV/CHIKV Control provides laboratories with a comprehensive, standardized external control for arbovirus molecular diagnostics. By combining inactivated Zika, Dengue (1–4), and Chikungunya viruses in plasma, this panel ensures accurate validation of the entire analytical process, strengthens laboratory quality assurance, and supports compliance with international accreditation requirements.