Helicobacter pylori Nucleic Acid Detection Kit (Fluorescence PCR)

For in vitro qualitative detection of Helicobacter pylori nucleic acid in gastric mucosal biopsy tissue or saliva samples from patients suspected of infection, serving as an auxiliary diagnostic tool for H. pylori-related disease.

SKU Code
AENE-OT075
Approval
On request
Product Type
Assay / Kit
Status
Available

For in vitro qualitative detection of Helicobacter pylori nucleic acid in gastric mucosal biopsy tissue or saliva samples from patients suspected of infection, serving as an auxiliary diagnostic tool for H. pylori-related disease.

Product typeAssay / Kit
Technology platformFluorescence PCR
Application areaGastrointestinal

Certificate

CE

Epidemiology

Helicobacter pylori (Hp) is a Gram-negative, spiral-shaped, microaerophilic bacterium. It has a worldwide presence and is strongly associated with numerous upper gastrointestinal disorders. Hp is a key pathogenic contributor to chronic gastritis, gastric and duodenal ulcers, and upper gastrointestinal cancers; the World Health Organization categorizes it as a Class I carcinogen. Deeper investigations reveal that Hp infection extends beyond the digestive system, playing a role in cardiovascular, cerebrovascular, and hepatobiliary diseases, chronic bronchitis, iron-deficiency anemia, and other systemic conditions, and it may even provoke tumor development.

SKU codeAENE-OT075
Storage≤-18℃ In dark
Shelf-life12 months
Specimen TypeHuman gastric mucosa tissue samples, Saliva
Ct≤38
CV≤5.0%
LoD500Copies/mL
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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