Influenza B Virus Nucleic Acid Quantitative Detection Kit (Fluorescence PCR)

Quantitative detection of Influenza B virus nucleic acid in human oropharyngeal swab samples for in vitro diagnostic use, aiding in the diagnosis of Influenza B infections.

SKU Code
AENE-RT140
Approval
On request
Product Type
Assay / Kit
Status
Available

Quantitative detection of Influenza B virus nucleic acid in human oropharyngeal swab samples for in vitro diagnostic use, aiding in the diagnosis of Influenza B infections.

Product typeAssay / Kit
Technology platformFluorescence PCR
Application areaRespiratory Infections

Epidemiology

Influenza, often called the flu, is an acute respiratory infection caused by the influenza virus. It is highly transmissible, primarily spreading through coughs and sneezes, and typically peaks during spring and winter. The virus has three types—Influenza A, B, and C—all members of the Orthomyxoviridae family. Types A and B are the main causes of human illness and consist of single-stranded, negative-sense, segmented RNA. Influenza B is further classified into two main lineages: Yamagata and Victoria. This type only undergoes antigenic drift, using mutations to escape immune detection and elimination. Its rate of evolution is slower than that of Influenza A, yet it can still trigger respiratory infections and lead to epidemics.

Work Flow

For sample extraction, a viral DNA/RNA kit (compatible with an automatic nucleic acid extractor) should be used, and all subsequent steps must be performed in strict accordance with the kit’s instructions for use.

SKU codeAENE-RT140
Storage≤-18℃
Shelf-life12 months
Specimen TypeOropharyngeal swab sample
CV5.0%
LoD500Copies/mL
SpecificityCross-reactivity: there is no cross reactivity between this kit and influenza A virus, adenovirus type 3, 7, human coronavirus SARSr-CoV, MERSr-CoV, HCoV-OC43, HCoV-229E, HCoV-HKU1, and HCoV-NL63, cytomegalovirus, enterovirus, parainfluenza virus, measles virus, human metapneumovirus, mumps virus, respiratory syncytial virus type B, rhinovirus, bordetella pertussis,chlamydia pneumoniae, corynebacterium, escherichia coli, haemophilus influenzae, jactobacillus, moraxella catarrhalis, avirulent mycobacterium tuberculosis, mycoplasma pneumoniae, neisseria meningitidis, neisseria gonorrhoeae, pseudomonas aeruginosa, staphylococcus aureus, staphylococcus epidermidis, streptococcus pneumoniae, streptococcus pyogenes, streptococcus salivarius and human genomic DNA.
Applicable InstrumentsApplied Biosystems 7500 Real-Time PCR System, Applied Biosystems 7500 Fast Real-Time PCR Systems, QuantStudio ® 5 Real-Time PCR Systems, SLAN-96P Real-Time PCR Systems(Hongshi Medical Technology Co. Ltd.), LightCycler ® 480 Real-Time PCR system, LineGene 9600 Plus Real-Time PCR Detection System (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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