

Fluorescence PCR · Others
Francisella tularensis Nucleic Acid Detection Kit (Fluorescence PCR)
Qualitative detection of Francisella tularensis nucleic acid in blood, lymph fluid, cultured isolates, and other specimens. For in vitro diagnostic use, aiding in the diagnosis of tularemia.
- SKU Code
AENE-OT017- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative detection of Francisella tularensis nucleic acid in blood, lymph fluid, cultured isolates, and other specimens. For in vitro diagnostic use, aiding in the diagnosis of tularemia.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Fluorescence PCR |
| Application area | Others |
Epidemiology
Francisella tularensis is a gram-negative coccus capable of causing tularemia, an acute infectious disease affecting both humans and animals. Owing to its high virulence and ease of transmission, the US CDC classifies it as a Class A bioterrorism pathogen.
Work Flow
A general DNA/RNA kit and an automatic nucleic acid extractor are used. Follow the manufacturer's instructions strictly. The recommended elution volume is 80 μL.
| SKU code | AENE-OT017 |
|---|---|
| Storage | -18℃ |
| Shelf-life | 12 months |
| Specimen Type | blood, lymph fluid, cultured isolates and other specimens |
| CV | ≤5.0% |
| LoD | 103 CFU/mL. |
| 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.
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