EBV Nucleic Acid Detection Kit (Fluorescence PCR)

This qualitative fluorescence PCR kit detects Epstein-Barr virus (EBV) DNA in human whole blood, plasma, and serum, aiding in the diagnosis of EBV-related conditions such as infectious mononucleosis.

SKU Code
AENE-OT061
Approval
On request
Product Type
Assay / Kit
Status
Available

This qualitative fluorescence PCR kit detects Epstein-Barr virus (EBV) DNA in human whole blood, plasma, and serum, aiding in the diagnosis of EBV-related conditions such as infectious mononucleosis.

Product typeAssay / Kit
Technology platformFluorescence PCR
Application areaRespiratory Infections

Certificate

CE

Epidemiology

Epstein-Barr virus (EBV), or human herpesvirus 4, is a widely prevalent herpesvirus. A growing body of evidence confirms that EBV contributes to the development and progression of multiple cancers, such as nasopharyngeal carcinoma, Hodgkin’s disease, T/natural killer cell lymphoma, Burkitt’s lymphoma, breast cancer, and gastric cancer. The virus is also intimately connected to post-transplant lymphoproliferative disorders, post-transplant smooth muscle tumors, AIDS-associated lymphoma, multiple sclerosis, primary central nervous system lymphoma, and leiomyosarcoma.

SKU codeAENE-OT061
Storage≤-18℃ In dark
Shelf-life12 months
Specimen TypeWhole blood, Plasma, Serum
Ct≤38
CV≤5.0%
LoD500Copies/mL
SpecificityIt has no cross-reactivity with other pathogens (such as human herpesvirus 1, 2, 3, 6, 7, 8, hepatitis B virus, cytomegalovirus, influenza A, etc.) or bacteria (Staphylococcus aureus, Candida albicans, etc.)
Applicable InstrumentsIt can match the mainstream fluorescent PCR instruments on the market. SLAN-96P Real-Time PCR Systems ABI 7500 Real-Time PCR Systems QuantStudio®5 Real-Time PCR Systems LightCycler®480 Real-Time PCR Systems LineGene 9600 Plus Real-Time PCR Detection Systems 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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