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
电子厂区3栋2楼
518103
+86 0755 27417763
info@ksbbiotech.com