Colloidal Gold · Pregnancy & Fertility
Follicle Stimulating Hormone (FSH) Detection Kit (Colloidal Gold)
This kit is a rapid chromatographic immunoassay for the qualitative detection of follicle stimulating hormone (FSH) in human urine, intended for in vitro diagnostic use as an aid in the assessment of fertility status.
- SKU Code
AENE-PF001- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
This kit is a rapid chromatographic immunoassay for the qualitative detection of follicle stimulating hormone (FSH) in human urine, intended for in vitro diagnostic use as an aid in the assessment of fertility status.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Colloidal Gold |
| Application area | Pregnancy & Fertility |
Certificate
CE
Epidemiology
Follicle-stimulating hormone (FSH) is a gonadotropin released by basophilic cells of the anterior pituitary gland. It is a glycoprotein with an approximate molecular weight of 30,000 daltons, composed of two noncovalently linked peptide subunits, alpha and beta. FSH secretion is controlled by gonadotropin-releasing hormone (GnRH) from the hypothalamus and is modulated via negative feedback by sex hormones from the target glands.
FSH concentrations rise during menopause, after surgical removal of the ovaries (oophorectomy), and in cases of premature ovarian failure. Disrupted relationships between luteinizing hormone (LH) and FSH, as well as between FSH and estrogen, are linked to conditions such as anorexia nervosa and polycystic ovary syndrome.
Work Flow
● Read the result (10-20 mins)
| SKU code | AENE-PF001 |
|---|---|
| Target region | Follicle Stimulating Hormone |
| Storage temperature | 4℃-30℃ |
| Sample type | Urine |
| Shelf life | 24 months |
| Auxiliary instruments | Not required |
| Extra Consumables | Not required |
| Detection time | 10-20 mins |
| 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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