Fluorescence PCR · Respiratory Infections
Influenza A Virus H3N2 Nucleic Acid Detection Kit (Fluorescence PCR)
This kit provides qualitative detection of influenza A virus H3N2 nucleic acid in nasopharyngeal swab specimens, aiding in the diagnosis of influenza caused by H3N2 strains.
- SKU Code
AENE-RT007- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
This kit provides qualitative detection of influenza A virus H3N2 nucleic acid in nasopharyngeal swab specimens, aiding in the diagnosis of influenza caused by H3N2 strains.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Fluorescence PCR |
| Application area | Respiratory Infections |
Work Flow
For sample extraction, a Viral DNA/RNA Kit (compatible with an Automatic Nucleic Acid Extractor) is suggested. All subsequent steps should be followed exactly as described in the kit's Instructions for Use (IFU).
| SKU code | AENE-RT007 |
|---|---|
| Storage | ≤-18℃ |
| Shelf-life | 9 months |
| Specimen Type | nasopharyngeal swab samples |
| Ct | ≤38 |
| CV | ≤5.0% |
| LoD | 500Copies/mL |
| Specificity | Repeatability: test the repeatability references by the kit, repeat the test for 10 times and CV≤5.0% is detected. Specificity: test the company negative references by the kit, and the test result meets the requirements. |
| Applicable Instruments | Applied Biosystems 7500 Real-Time PCR Systems Applied Biosystems 7500 Fast Real-Time PCR Systems QuantStudio ® 5 Real-Time PCR Systems SLAN-96P Real-Time PCR Systems (Hongshi Medical Technology Co. Ltd.) LightCycler ® 480 Real-Time PCR system LineGene 9600 Plus Real-Time PCR Detection Systems (FQD-96A, Hangzhou Bioer technology) MA-6000 Real-Time Quantitative Thermal Cycler (Suzhou Molarray Co. Ltd.) BioRad CFX96 Real-Time PCR System BioRad CFX Opus 96 Real-Time PCR 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.
Inquiry
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