Influenza A (Flu A)

PDB ID: 2IQH. Source: RCSB Protein Data Bank. For illustration purposes only.

VeriGoldTM Flu A

The VeriGoldTM Influenza A Rapid Diagnostic Test is an in vitro immunochromatographic assay for the qualitative detection of Influenza type A viral antigen in nasal swab, throat swab, or nasal wash/aspirate specimens. This test is intended to aid in the rapid differential diagnosis of Influenza A infections, providing results within minutes to support early clinical decision-making during flu season or suspected outbreaks.

The test is intended for professional and laboratory use only. Negative results should be interpreted in conjunction with clinical findings and may require confirmation by additional methods, as they do not exclude Influenza A infection and should not be used as the sole basis for treatment or other management decisions.

Ref. Code 808049
Analyte Influenza A virus nucleoprotein antigen
Format POCT rapid test (cassette / cartridge)
Diagnostic Readout Qualitative
Reading Time 15 minutes
Measuring Range Not applicable
Cut-off Value Not applicable
Sensitivity / Specificity 97.5% / 99.5%
Storage Conditions 2–30°C
Shelf Life 18 months
Certificate CE
Sample Types Nasal swab, throat swab, or nasal wash/aspirate specimens
Sample Volume 100 µL (3 drops) of extraction mixture
Collection Method Nasal swab, throat swab, or nasal wash/aspirate specimen collection
Sample Stability Stable for testing within 1 hour at room temperature (as validated)
Acceptable Anticoagulants EDTA / Heparin / Citrate (as applicable)
Notes on Handling Specimens should be collected and handled using standard laboratory procedures. Use fresh samples when possible and avoid hemolyzed, lipemic, or contaminated specimens.
Detection Method Immunochromatography
Antibody Format Monoclonal / sandwich
Signal Generation Colloidal gold
Reading Method Visual
Mechanism The assay is based on an immunochromatographic lateral flow principle, in which Influenza A viral antigens present in the respiratory specimen bind to specific labeled antibodies during migration along the membrane by capillary action. The resulting antigen–antibody complexes are captured by immobilized antibodies at the test line, producing a visible signal indicating the presence of Influenza A antigen in the sample.
Tests per Kit 10/20/50/100 Tests
Dimension of Kit Box 21 × 13.5 × 8cm
Boxes per Carton 48 Kits
Tests per Carton (Bulk) 960 Tests
G.W. per Carton (Boxed) 23.2 kg
G.W. per Carton (Bulk) 26.2 kg
Carton Dimension 67 × 57.5 × 39 cm
Carton Volume 0.15 CBM
Packaging Format Individual sealed test kits / bulk configuration (as applicable)
Items Included - 20 test cassettes
- Extraction solution
- Instructions for Use
Storage & Shipping Conditions Standard ambient transport; store according to product label requirements

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深圳市康生保
生物技术有限公司

深圳市宝安区

福海 街道

新和 社区 安达

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518103

 

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