Colloidal Gold · Respiratory Infections
SARS-CoV-2, Respiratory Syncytial Virus, and Influenza A/B Antigen Combined Detection Kit (Colloidal Gold)
For in vitro qualitative detection of SARS-CoV-2, respiratory syncytial virus, and influenza A/B antigens to aid in the differential diagnosis of COVID-19, RSV, and influenza infections.
- SKU Code
AENE-RT152- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
For in vitro qualitative detection of SARS-CoV-2, respiratory syncytial virus, and influenza A/B antigens to aid in the differential diagnosis of COVID-19, RSV, and influenza infections.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Colloidal Gold |
| Application area | Respiratory Infections |
Certificate
CE
Epidemiology
The illness known as COVID-19 (originally called novel coronavirus pneumonia in 2019) is a respiratory disease caused by the SARS-CoV-2 virus.
Respiratory syncytial virus (RSV) often causes upper and lower respiratory infections and is the primary cause of bronchiolitis and pneumonia in infants.
Influenza viruses are categorized into types A, B, C, and D based on antigenic differences in the nucleoprotein (NP) and matrix protein (M). Types A and B are the main human influenza pathogens, characterized by widespread epidemics and high infectivity, and they can lead to serious, life-threatening infections in children, the elderly, and people with weakened immune systems.
Work Flow
Acceptable specimen types:
- Nasopharyngeal swab samples
- Oropharyngeal swab sample
- Nasal swab samples
Precautions: 1. Do not interpret results after 20 minutes. 2. Use the product within 1 hour of opening. 3. Add samples and buffers strictly per the instructions.
| SKU code | AENE-RT152 |
|---|---|
| Target region | SARS-CoV-2, Respiratory Syncytium, Influenza A&B Antigen |
| Storage temperature | 4-30 ℃ sealed and dry for storage |
| Sample type | Nasopharyngeal swab、Oropharyngeal swab、Nasal swab |
| Shelf life | 24 months |
| Auxiliary instruments | Not required |
| Extra Consumables | Not required |
| Detection time | 15-20 mins |
| 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.
Inquiry
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