The Flu A B Influenza Virus Ag Diagnostic Rapid Test Kit is a professional-grade lateral flow immunoassay designed for the rapid and accurate detection of Influenza A and B antigens. Utilizing highly specific monoclonal antibodies, this diagnostic tool provides a critical first line of defense in differentiating seasonal flu strains from other respiratory infections, ensuring timely clinical intervention and patient management.
Engineered for versatility and precision, the kit supports multiple specimen types including nasal swabs, throat swabs, and nasal aspirates. With an accuracy rate exceeding 99%, it is an essential asset for healthcare providers, clinics, and diagnostic laboratories seeking a reliable, high-sensitivity solution for rapid influenza screening without the need for complex laboratory infrastructure.
Detailed Parameters
| Product Name | Influenza A/B Rapid Test | Accuracy | >99% |
|---|---|---|---|
| Specimen Types | Nasal Swab / Throat Swab / Nasal Aspirate | Shelf Life | 24 Months |
| Storage Temp | 2-30°C (36-86°F) | Flu A Sensitivity | 3.5×10⁴ TCID₅₀/ml |
| Flu B Sensitivity | 1.5×10⁵ TCID₅₀/ml | Analytical LOD (A H1N1) | 2.075 ngHA/mL |
| Analytical LOD (A H3N2) | 5.5 ngHA/mL | Analytical LOD (B) | 78 ng/mL |
Key Advantages
High Precision
Achieves over 99% accuracy using specialized monoclonal antibodies for pinpoint detection of viral antigens.
Rapid Results
Delivers fast diagnostic outcomes, allowing for immediate clinical decisions and reduced patient waiting times.
Multi-Specimen Use
Flexible sampling via nasal swabs, throat swabs, or nasal aspirates to suit various patient needs.
Clear Readout
Easy-to-interpret visual results on the plastic cassette, minimizing the risk of human error during reading.
Strong Sensitivity
Highly sensitive detection limits for H1N1, H3N2, and Influenza B strains for early-stage detection.
Stable Storage
Long-term stability of 24 months when stored at 2-30°C, simplifying supply chain management.
Product Gallery
Management Platforms
Complete Kit Provision
Includes test devices, extraction buffers, sterilized swabs, and filter caps for end-to-end testing.
Quality Control
Strict adherence to manufacturing standards ensuring each batch meets high sensitivity and specificity.
Rapid Turnaround
Optimized workflow from specimen collection to result reading to accelerate patient throughput.
Sterile Packaging
Individual foil pouches ensure contamination-free components and prolonged shelf-life.
Bulk Supply Options
Available in flexible packaging including 25 pcs per inner bag or box for scalable procurement.
Protocol Support
Comprehensive Instructions for Use (IFU) included to ensure standardized operation across clinics.
Investment Return Comparison
| Feature | Rapid Test Kit | Traditional Lab PCR |
|---|---|---|
| Turnaround Time | 15-30 Minutes | 24-72 Hours |
| Cost per Test | Low / Affordable | High / Expensive |
| Equipment Needed | None / Point-of-Care | Complex Thermal Cyclers |
| Operational Skill | Basic Training | Specialized Technician |
| Patient Throughput | Very High | Limited by Batching |
Frequently Asked Questions
Our rapid test offers over 99% accuracy for antigen detection, providing immediate results. While PCR is the gold standard for viral load, this kit is highly effective for rapid screening and immediate clinical triage.
The kit is validated for nasal swabs, throat swabs, and nasal aspirates. The choice depends on the clinician's preference and the patient's current symptomatic presentation.
The kits should be stored in their sealed foil pouches at temperatures between 2-30°C (36-86°F). It is critical not to freeze the product to maintain reagent integrity.
Yes, the test uses specific monoclonal antibodies to independently identify antigens for both Influenza Type A and Type B, providing a clear differential diagnosis.
The product has a shelf life of 24 months from the date of manufacture, provided it is stored according to the specified temperature guidelines.
Yes, the kit includes professional-grade sterilized swabs for sample collection to ensure that the results are not compromised by external contamination.
