Enterovirus Universal, EV71, and CoxA16 Nucleic Acid Detection Kit (Fluorescence PCR)

For in vitro qualitative detection of enterovirus, EV71, and CoxA16 nucleic acids in oropharyngeal swabs and herpes fluid samples, aiding diagnosis of hand-foot-mouth disease.

SKU Code
AENE-EV010
Approval
On request
Product Type
Assay / Kit
Status
Available

For in vitro qualitative detection of enterovirus, EV71, and CoxA16 nucleic acids in oropharyngeal swabs and herpes fluid samples, aiding diagnosis of hand-foot-mouth disease.

Product typeAssay / Kit
Technology platformFluorescence PCR
Application areaGastrointestinal

Epidemiology

Hand-foot-mouth disease is an infectious illness triggered by enteroviruses. There are 108 known serotypes, classified into four groups: A, B, C, and D. The primary pathogens are enterovirus EV71 and CoxA16. The condition predominantly affects children under 5 years, causing vesicular lesions on hands, feet, and oral cavity. A minority may develop severe complications such as myocarditis, pulmonary edema, and aseptic meningoencephalitis.

Work Flow

Extraction is performed using a Viral DNA/RNA Kit and an Automatic Nucleic Acid Extractor, following the manufacturer’s instructions. The sample input volume is 200μl, and the suggested elution volume is 80μl.

SKU codeAENE-EV010
Storage-18℃
Shelf-life9 months
Specimen TypeO ropharyngeal swabs,H erpes fluid 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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