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 typeAssay / Kit
Technology platformFluorescence PCR
Application areaOthers

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 codeAENE-OT017
Storage-18℃
Shelf-life12 months
Specimen Typeblood, lymph fluid, cultured isolates and other specimens
CV≤5.0%
LoD103 CFU/mL.
Applicable InstrumentsApplicable 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.
ApprovalOn request
DocumentsDatasheet, 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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