

Colloidal Gold · Gastrointestinal
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 type | Assay / Kit |
|---|---|
| Technology platform | Colloidal Gold |
| Application area | Gastrointestinal |
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 code | AENE-OT058 |
|---|---|
| Target region | Helicobacter pylori |
| Storage temperature | 4℃-30℃ |
| Sample type | Stool |
| Shelf life | 24 months |
| Auxiliary instruments | Not required |
| Extra Consumables | Not required |
| Detection time | 10-15 mins |
| Specificity | There 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. |
| Approval | On request |
|---|---|
| Documents | Datasheet, 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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