Colloidal Gold · Pregnancy & Fertility
Human Chorionic Gonadotropin (HCG) Detection Kit (Colloidal Gold Immunochromatography)
This product is an in vitro qualitative test for detection of human chorionic gonadotropin (HCG) in human urine. It is intended to aid in the early detection of pregnancy.
- SKU Code
AENE-PF003- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
This product is an in vitro qualitative test for detection of human chorionic gonadotropin (HCG) in human urine. It is intended to aid in the early detection of pregnancy.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Colloidal Gold |
| Application area | Pregnancy & Fertility |
Certificate
CE/FDA 510K
Epidemiology
Human chorionic gonadotropin (HCG) is a glycoprotein hormone consisting of α and β subunits, produced by placental trophoblast cells. Shortly after fertilization, HCG secretion commences. Once trophoblast cells generate sufficient amounts, the hormone enters the bloodstream and is excreted in urine. Consequently, measuring HCG in urine specimens serves as a supportive diagnostic tool for early pregnancy.
Work Flow
- Test strip
- Test cassette
- Test pen
- Read results (10–15 minutes)
| SKU code | AENE-PF003 |
|---|---|
| Target region | HCG |
| Storage temperature | 4℃-30℃ |
| Sample type | Urine |
| Shelf life | 24 months |
| Auxiliary instruments | Not required |
| Extra Consumables | Not required |
| Detection time | 5-10 mins |
| Specificity | Test the human luteinizing hormone (hLH) with concentration of 500mIU/mL, the human follicle stimulating hormone (hFSH) with concentration of 1000mIU/mL and the human thyrotropin (hTSH) with concentration of 1000μIU/mL, and the results are negative. |
| 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.
Inquiry
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