Monkeypox Virus Nucleic Acid Detection Kit (Fluorescence PCR)

This kit is used for in vitro qualitative detection of monkeypox virus nucleic acid in human rash fluid, nasopharyngeal swabs, throat swabs and serum samples.

SKU Code
AENE-OT071
Approval
On request
Product Type
Assay / Kit
Status
Available

This kit is used for in vitro qualitative detection of monkeypox virus nucleic acid in human rash fluid, nasopharyngeal swabs, throat swabs and serum samples.

Product typeAssay / Kit
Technology platformFluorescence PCR
Application areaOthers

Certificate

CE

Epidemiology

Monkeypox (MP) is an acute zoonotic infection caused by the Monkeypox Virus (MPV). Transmission predominantly occurs from animals to humans through bites or direct exposure to the blood, body fluids, or pox lesions of infected animals. Human-to-human spread happens via respiratory droplets during extended close face-to-face contact, or by touching a patient's body fluids or contaminated items.

The clinical presentation resembles smallpox, with an incubation period typically around 12 days. Initial signs include fever, headache, muscle and back pain, swollen lymph nodes, fatigue, and malaise. A rash emerges 1 to 3 days after fever onset, often starting on the face and then appearing elsewhere. The illness lasts 2 to 4 weeks, with a case fatality rate between 1% and 10%. Lymphadenopathy is a key clinical feature that differentiates monkeypox from smallpox.

SKU codeAENE-OT071
StorageLiquid: ≤-18℃ In dark; Lyophilized: ≤30℃ In dark
Shelf-life12 months
Specimen TypeRash Fluid, Nasopharyngeal Swab, Throat Swab, Serum
Ct≤38
CV≤5.0 %
LoD200Copies/mL
SpecificityNo cross-reactivity with Smallpox virus, Cowpox virus, Vaccinia virus, Herpes simplex virus, etc. No cross-reactivity with other pathogens that cause rash disease. No cross-reactivity with human genomic DNA.
Applicable InstrumentsIt can match the mainstream fluorescent PCR instruments on the market. ABI 7500 Real-Time PCR Systems QuantStudio® 5 Real-Time PCR Systems SLAN-96P 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
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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