Freeze-dried Zaire and Sudan Ebolavirus Nucleic Acid Detection Kit (Fluorescence PCR)

For detecting and typing Zaire and Sudan Ebolavirus RNA in serum or plasma from individuals with suspected infection.

SKU Code
AENE-FE035
Approval
On request
Product Type
Assay / Kit
Status
Available

For detecting and typing Zaire and Sudan Ebolavirus RNA in serum or plasma from individuals with suspected infection.

Product typeAssay / Kit
Technology platformFluorescence PCR
Application areaFebrile Encephalitis

Epidemiology

Ebolavirus is a member of the Filoviridae family, characterized as an unsegmented, single-stranded, negative-sense RNA virus. Virions are filamentous, averaging 1000 nm in length and approximately 100 nm in diameter. The viral genome is a single, negative-sense RNA strand of 18.9 kb that codes for seven structural and one non-structural protein. Species include Zaire, Sudan, Bundibugyo, Tai Forest, and Reston. The Zaire and Sudan species are known to cause fatal human outbreaks. Ebola hemorrhagic fever (EHF) is a severe, often fatal illness. Transmission to humans occurs through direct contact with bodily fluids, secretions, or excretions from infected individuals or animals. Clinically, it presents with abrupt fever, hemorrhage, and multiorgan failure. Case fatality rates range from 50% to 90%. Laboratory diagnosis relies on etiological and serological methods. Etiological testing includes ELISA for viral antigens in blood, nucleic acid amplification (e.g., RT-PCR), and virus isolation in cell lines such as Vero and HeLa. Serological testing involves capture ELISA for serum-specific IgM antibodies, and ELISA or immunofluorescence for serum-specific IgG antibodies.

Work Flow

A viral DNA/RNA extraction kit is used together with an automated nucleic acid extractor. Follow the kit instructions for the procedure: use a sample volume of 200 µL and an elution volume of 80 µL.

SKU codeAENE-FE035
Storage≤30℃
Shelf-life12 months
Specimen Typeserum,pla sma samples
CV≤5.0%
LoD500 Copies/μL
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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