Hepatitis B Virus Nucleic Acid Detection Kit (Fluorescence PCR)

This kit is used for in vitro quantitative detection of hepatitis B virus (HBV) nucleic acid in human serum samples, aiding in the diagnosis and monitoring of HBV infection, which can lead to liver cirrhosis or hepatocellular carcinoma.

SKU Code
AENE-HP001
Approval
On request
Product Type
Assay / Kit
Status
Available

This kit is used for in vitro quantitative detection of hepatitis B virus (HBV) nucleic acid in human serum samples, aiding in the diagnosis and monitoring of HBV infection, which can lead to liver cirrhosis or hepatocellular carcinoma.

Product typeAssay / Kit
Technology platformFluorescence PCR
Application areaHepatitis

Epidemiology

Hepatitis B, caused by the hepatitis B virus (HBV), is a contagious illness that damages the liver and may affect multiple organs. Common symptoms include profound tiredness, loss of appetite, swelling of the legs or entire body, and enlargement of the liver. Among adults infected, 5% are unable to clear the virus effectively, leading to chronic infection; this figure rises to 95% for children infected by their mothers. Persistent HBV infection can result in liver cirrhosis or hepatocellular carcinoma.

SKU codeAENE-HP001
Storage≤-18℃ In dark
Shelf-life12 months
Specimen TypeVenous blood
Ct≤33
CV≤5.0%
LoD25IU/mL
SpecificityThere is no cross-reactivity with Cytomegalovirus, EB virus, HIV, HAV, Syphilis, Human Herpesvirus-6, HSV-1/2, Influenza A, Propionibacterium Acnes, Staphylococcus Aureus and Candida albican
Applicable InstrumentsIt can match the mainstream fluorescent PCR instruments on the market. ABI 7500 Real-Time PCR Systems ABI 7500 Fast Real-Time PCR Systems SLAN-96P 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 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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