

Isothermal Amplification · Respiratory Infections
Influenza A Virus Nucleic Acid Detection Kit (Isothermal Amplification)
This kit is intended for the qualitative detection of Influenza A virus nucleic acid in human pharyngeal swab specimens. It aids in the diagnosis of Influenza A infection.
- SKU Code
AENE-RT049A- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
This kit is intended for the qualitative detection of Influenza A virus nucleic acid in human pharyngeal swab specimens. It aids in the diagnosis of Influenza A infection.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Isothermal Amplification |
| Application area | Respiratory Infections |
Certificate
CE
Epidemiology
Influenza virus, a key member of Orthomyxoviridae, poses a severe threat to human health and infects a broad range of hosts. Seasonal epidemics impact roughly 600 million individuals globally each year and result in 250,000 to 500,000 deaths, with influenza A virus being the primary cause of both infection and mortality. Influenza A virus possesses a single-stranded negative-sense RNA genome. Based on surface hemagglutinin (HA) and neuraminidase (NA), HA subtypes are classified into 16 types and NA into 9 types. Among influenza A viruses, the subtypes capable of direct human infection include A H1N1, H3N2, H5N1, H7N1, H7N2, H7N3, H7N7, H7N9, H9N2, and H10N8. Of these, the H1, H3, H5, and H7 subtypes are highly pathogenic, with H1N1, H3N2, H5N7, and H7N9 being particularly noteworthy. The antigenicity of influenza A virus is prone to variation, allowing new subtypes to emerge and trigger global pandemics. Starting in March 2009, a novel H1N1 influenza A outbreak began in Mexico and the United States and subsequently spread worldwide. Influenza A virus can be transmitted through multiple routes, including the digestive and respiratory tracts, damaged skin, and the eyes and conjunctiva. Post-infection symptoms mainly include high fever, cough, runny nose, and myalgia, often accompanied by severe pneumonia. In severe cases, organ failure of the heart, kidneys, and other organs can lead to death, resulting in a high fatality rate. Consequently, there is an urgent clinical need for a simple, accurate, and rapid diagnostic method for influenza A virus to guide medication and diagnosis.
Work Flow
Option 1: The recommended extraction process uses a Viral DNA/RNA Kit paired with an automatic nucleic acid extractor.
Option 2: Alternatively, employ a nucleic acid extraction or purification reagent (YDP302).
| SKU code | AENE-RT049A |
|---|---|
| Storage | Liquid: ≤-18℃ In dark; Lyophilized: ≤30℃ In dark |
| Shelf-life | Liquid: 9 months; Lyophilized: 12 months |
| Specimen Type | Freshly collected throat swabs |
| CV | ≤10.0% |
| Tt | ≤40 |
| LoD | 1000C opies/ mL |
| Specificity | T here is no cross-reactivity with Influenza B, Staphylococcus aureus, Streptococcus (including Streptococcus pneumoniae), Adenovirus, Mycoplasma pneumoniae, Respiratory Syncytial Virus, Mycobacterium tuberculosis, Measles, Haemophilus influenzae, Rhinovirus, Coronavirus, Enteric Virus, swab of healthy person. |
| Applicable Instruments | : Applied Biosystems 7500 Real-Time PCR Systems SLAN ® -96P Real-Time PCR Systems LightCycler® 480 Real-Time PCR system Easy Amp Real-time Fluorescence Isothermal Detection System() |
| Approval | On request |
|---|---|
| Documents | Datasheet, IFU, SDS, COA / conformance, origin, and export documents where available |
FAQ
What should be confirmed before quotation?
Sample context, collection method, and extraction workflow should be confirmed before final kit selection.
Which documents can be requested?
Datasheet, IFU, SDS, COA / conformance, origin, insurance, and export documents can be checked where available.
Can the format be adjusted for different workflows?
Liquid or lyophilized format options should be confirmed together with instrument compatibility and shipment requirements.
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