Influenza A/B Detection Kit
£560.00
The geneMAP™ Influenza A/B Detection Kit is a sophisticated diagnostic tool designed to rapidly and accurately detect Influenza virus types A and B using one-step multiplex real-time PCR technology. Certified by CE-IVD and compatible with FAM, VIC/HEX, and Cy5 three-color real-time PCR instruments, this kit offers superior analytical sensitivity and specificity. It plays a crucial role in the prompt diagnosis of influenza, facilitating early therapeutic intervention and aiding in the identification and management of influenza outbreaks, particularly in vulnerable populations such as the elderly and immunocompromised individuals.
- High Sensitivity and Specificity: Ensures reliable detection of Influenza A and B viruses, minimizing false positives and negatives.
- One-Step Multiplex Real-Time PCR Technology: Simplifies the testing process, allowing for the simultaneous detection of both influenza types in a single assay.
- Three-Color Compatibility: Designed for use with real-time PCR instruments that support FAM, VIC/HEX, and Cy5, enhancing assay flexibility.
- CE-IVD Certification: Meets the highest European standards for in vitro diagnostic medical devices.
- Diagnosis of Influenza: Critical for the detection of Influenza A and B viruses in individuals presenting with symptoms of influenza-like illness.
- Public Health Surveillance: Supports health authorities in monitoring influenza activity and implementing control measures during the flu season.
- Technology: Utilizes one-step multiplex real-time PCR for the concurrent detection of Influenza A and B viruses.
- Compatibility: Suitable for real-time PCR instruments supporting FAM, VIC/HEX, and Cy5 detection channels.
- Certification: Carries the CE-IVD mark, indicating compliance with EU regulations for in vitro diagnostic use.
- High Sensitivity and Specificity: Ensures reliable detection of Influenza A and B viruses, minimizing false positives and negatives.
- One-Step Multiplex Real-Time PCR Technology: Simplifies the testing process, allowing for the simultaneous detection of both influenza types in a single assay.
- Three-Color Compatibility: Designed for use with real-time PCR instruments that support FAM, VIC/HEX, and Cy5, enhancing assay flexibility.
- CE-IVD Certification: Meets the highest European standards for in vitro diagnostic medical devices.
- Diagnosis of Influenza: Critical for the detection of Influenza A and B viruses in individuals presenting with symptoms of influenza-like illness.
- Public Health Surveillance: Supports health authorities in monitoring influenza activity and implementing control measures during the flu season.
- Technology: Utilizes one-step multiplex real-time PCR for the concurrent detection of Influenza A and B viruses.
- Compatibility: Suitable for real-time PCR instruments supporting FAM, VIC/HEX, and Cy5 detection channels.
- Certification: Carries the CE-IVD mark, indicating compliance with EU regulations for in vitro diagnostic use.
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