

Colloidal Gold · Gastrointestinal
Clostridium difficile Glutamate Dehydrogenase (GDH) and Toxin A/B Detection Kit (Colloidal Gold)
For qualitative detection of Clostridium difficile glutamate dehydrogenase (GDH) and toxins A/B in stool specimens to aid in the diagnosis of C. difficile infection.
- SKU Code
AENE-EV030A- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
For qualitative detection of Clostridium difficile glutamate dehydrogenase (GDH) and toxins A/B in stool specimens to aid in the diagnosis of C. difficile infection.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Colloidal Gold |
| Application area | Gastrointestinal |
Certificate
CE
Epidemiology
Clostridium difficile (CD) is a gram-positive, obligate anaerobic bacillus that normally resides in the human body. When high-dose antibiotics suppress competing flora, CD can proliferate extensively. The species includes both toxigenic and non-toxigenic strains. All CD strains produce glutamate dehydrogenase (GDH) during replication, but only those that produce toxins are disease-causing. Toxigenic strains secrete two exotoxins: toxin A and toxin B. Toxin A, an enterotoxin, induces intestinal wall inflammation, cellular infiltration, increased permeability, hemorrhage, and necrosis. Toxin B, a cytotoxin, disrupts the cytoskeleton, causes cellular pyknosis and necrosis, and directly injures intestinal parietal cells, leading to diarrhea and pseudomembranous colitis.
| SKU code | AENE-EV030A |
|---|---|
| Target region | Glutamate Dehydrogenase(GDH) and Toxin A/B |
| Storage temperature | 4℃-30℃ |
| Sample type | stool |
| Shelf life | 24 months |
| Auxiliary instruments | Not required |
| Extra Consumables | Not required |
| Detection time | 10-15mins |
| 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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