Fluorescence PCR · Meningitis
Yellow Fever Virus Nucleic Acid Detection Kit (Fluorescence PCR)
Qualitative detection of Yellow Fever virus nucleic acid in human serum samples to aid in the clinical diagnosis and management of Yellow Fever virus infection.
- SKU Code
AENE-FE012- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative detection of Yellow Fever virus nucleic acid in human serum samples to aid in the clinical diagnosis and management of Yellow Fever virus infection.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Fluorescence PCR |
| Application area | Meningitis |
Certificate
CE
Epidemiology
Yellow fever virus is classified under Togavirus Group B and is an RNA virus. It is spherical with a size of approximately 20–60 nm. Following entry into the human body, the virus travels to regional lymph nodes, where it undergoes replication. After a few days, it enters the bloodstream, causing viremia, and primarily affects the liver, spleen, kidneys, lymph nodes, bone marrow, and striated muscles. Subsequently, the virus becomes undetectable in the blood but may still be found in the spleen, bone marrow, and lymph nodes.
| SKU code | AENE-FE012 |
|---|---|
| Storage | Liquid: ≤-18℃ In dark; Lyophilized: ≤30℃ In dark |
| Shelf-life | Liquid: 9 months; Lyophilized: 12 months |
| Specimen Type | fresh serum |
| CV | ≤5.0% |
| Ct | ≤38 |
| LoD | 500Copies/mL |
| Specificity | Use the kit to test the company negative control and the results should meet the corresponding requirements. |
| Applicable Instruments | : Applied Biosystems 7500 Real-Time PCR Systems Applied Biosystems 7500 Fast Real-Time PCR Systems SLAN ®-96P Real-Time PCR Systems QuantStudio™ 5 Real-Time PCR Systems LightCycler®480 Real-Time PCR system LineGene 9600 Plus Real-Time PCR Detection System MA-6000 Real-Time Quantitative Thermal Cycler 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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