Fluorescence PCR · Respiratory Infections
Rubella Virus Nucleic Acid Detection Kit (Fluorescence PCR)
Qualitative detection of rubella virus nucleic acid in oropharyngeal swabs and herpes fluid samples. Aids in the diagnosis of rubella infection, crucial for screening during pregnancy to prevent congenital rubella syndrome.
- SKU Code
AENE-RT027- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative detection of rubella virus nucleic acid in oropharyngeal swabs and herpes fluid samples. Aids in the diagnosis of rubella infection, crucial for screening during pregnancy to prevent congenital rubella syndrome.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Fluorescence PCR |
| Application area | Respiratory Infections |
Epidemiology
Rubella virus is the sole species within the Rubivirus genus, belonging to the Togaviridae family. Infection during early pregnancy can lead to congenital rubella syndrome (CRS) in the fetus, resulting in malformations and abnormal functional development across multiple organs.
Work Flow
The procedure uses a Viral DNA/RNA Kit compatible with automated nucleic acid extractors, as well as a Viral DNA/RNA Kit for manual processing. The sample extraction volume is 200 µL, and the recommended elution volume is 150 µL.
| SKU code | AENE-RT027 |
|---|---|
| Storage | ≤-18℃ |
| Shelf-life | 12 months |
| Specimen Type | herpes fluid，oropharyngeal swabs |
| Ct | ≤38 |
| CV | 5.0% |
| LoD | 500 Copies/μL |
| Applicable Instruments | Applicable to type I detection reagent: Applied Biosystems 7500 Real-Time PCR Systems, QuantStudio ® 5 Real-Time PCR Systems, SLAN-96P Real-Time PCR Systems (Hongshi Medical Technology Co. Ltd.), 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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