Measles Virus Nucleic Acid Detection Kit (Fluorescence PCR)

Qualitative detection of measles virus (MeV) nucleic acid in oropharyngeal swabs and herpes fluid samples. For in vitro diagnostic use in the diagnosis of measles.

SKU Code
AENE-RT028
Approval
On request
Product Type
Assay / Kit
Status
Available

Qualitative detection of measles virus (MeV) nucleic acid in oropharyngeal swabs and herpes fluid samples. For in vitro diagnostic use in the diagnosis of measles.

Product typeAssay / Kit
Technology platformFluorescence PCR
Application areaRespiratory Infections

Epidemiology

Measles is an acute respiratory illness caused by the measles virus, marked by fever, inflammation of the upper respiratory tract, conjunctivitis, a characteristic skin rash of red macules, and Koplik spots on the buccal mucosa. Infected individuals are the sole reservoir of the virus, which spreads via respiratory droplets; the general population is universally susceptible. The virus's high infectivity and rapid transmission can lead to outbreaks, making measles a significant threat to childhood health and survival.

Work Flow

The procedure uses a Viral DNA/RNA Kit that is compatible with an Automatic Nucleic Acid Extractor. A sample volume of 200 µL is extracted, and the recommended elution volume is 150 µL.

SKU codeAENE-RT028
Storage-18℃
Shelf-life12 months
Specimen Typeherpes fluid,oropharyngeal swabs
Ct≤38
CV5.0%
LoD500Copies/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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