Helicobacter pylori Antigen Detection Kit (Colloidal Gold)

For in vitro qualitative detection of Helicobacter pylori antigen in human stool specimens, supporting auxiliary diagnosis of H. pylori infection in gastric diseases.

SKU Code
AENE-OT058
Approval
On request
Product Type
Assay / Kit
Status
Available

For in vitro qualitative detection of Helicobacter pylori antigen in human stool specimens, supporting auxiliary diagnosis of H. pylori infection in gastric diseases.

Product typeAssay / Kit
Technology platformColloidal Gold
Application areaGastrointestinal

Certificate

CE

Epidemiology

Globally, Helicobacter pylori (Hp) is a primary cause of gastritis, peptic ulcers, and gastric cancer. This Gram-negative bacterium is a member of the Helicobacter family. Carriers shed H. pylori in their feces, and transmission occurs via fecal-oral, oral-oral, and pet-to-human pathways. Once inside the host, the bacterium multiplies in the gastric mucosa of the pyloric region, disrupting the gastrointestinal tract and leading to ulcer formation.

Work Flow

● Read the result (10-15 mins)

SKU codeAENE-OT058
Target regionHelicobacter pylori
Storage temperature4℃-30℃
Sample typeStool
Shelf life24 months
Auxiliary instrumentsNot required
Extra ConsumablesNot required
Detection time10-15 mins
SpecificityThere is no cross-reactivity with Campylobacter, Bacillus, Escherichia, Enterobacter, Proteus, Candida albicans, Enterococcus, Klebsiella, human infection with other Helicobacter, Pseudomonas, Clostridium, Staphylococcus, Streptococcus, Salmonella, Acinetobacter, Fusobacterium, Bacteroides.
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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