Colloidal Gold · Pregnancy & Fertility
Fetal Fibronectin (fFN) Detection Kit (Colloidal Gold Immunochromatography)
Qualitative detection of fetal fibronectin (fFN) in human cervical vaginal secretions.
- SKU Code
AENE-PF002- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative detection of fetal fibronectin (fFN) in human cervical vaginal secretions.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Colloidal Gold |
| Application area | Pregnancy & Fertility |
Certificate
CE
Epidemiology
Preterm birth is defined as delivery between 28 and 37 weeks of gestation. It is the leading cause of death and disability among non-hereditary perinatal conditions. Symptoms include uterine contractions, changes in vaginal discharge, vaginal bleeding, back pain, abdominal discomfort, pelvic pressure, and cramping.
Fetal fibronectin (fFN) is a fibronectin isoform, a complex glycoprotein with a molecular weight of approximately 500 kDa. In pregnant women exhibiting symptoms, an fFN level of 50 ng/mL or higher in cervicovaginal secretions, collected between 24 weeks 0 days and 34 weeks 6 days, indicates an increased risk of preterm delivery within 7 to 14 days of testing. In asymptomatic pregnant women, an elevated fFN level between 22 weeks 0 days and 30 weeks 6 days signals a heightened risk of preterm birth before 34 weeks 6 days.
Work Flow
Read the result (10-20 mins)
| SKU code | AENE-PF002 |
|---|---|
| Target region | Fetal Fibronectin |
| Storage temperature | 4℃-30℃ |
| Sample type | Vaginal secretions |
| 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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