Diagnostic Kit for free β‑subunit of human chorionic gonadotropin
Diagnostic Kit for Human Chorionic Gonadoteopin (Colloidal Gold)
| Model Number | HCG | Packing | 25 Tests/ kit, 30kits/CTN |
| Name | Diagnostic Kit for free β‑subunit of human chorionic gonadotropin | Instrument classification | Class I |
| Features | High sensitivity, Easy opeation | Certificate | CE/ ISO13485 |
| Accuracy | > 99% | Shelf life | Two Years |
| Methodology | fluorescence immunochromatographic assay | OEM/ODM service | Avaliable |
Test procedure
| 1 | Open the aluminum foil bag package of reagent and take out the test device. Horizontally insert the test device into the slot of immune analyzer. |
| 2 | On home page of operation interface of immune analyzer, click “Standard” to enter test interface. |
| 3 | Click “QC Scan” to scan the QR code on inner side of the kit; input kit related parameters into instrument and select sample type. |
| 4 | Check the consistency of “Product Name”, “Batch Number” etc. on test interface with information on the kit marker |
| 5 | After information consistency is confirmed, take out sample diluents, add 20µL of serum sample, and mix well |
| 6 | Add 80µL of above mixed solution into the sample hole of test device. |
| 7 | After complete sample addition, click “Timing” and remaining test time will be automatically displayed on the interface. |
Intend Use
This kit is applicable to in vitro quantitative detection of free β-subunit of human chorionic gonadotropin (F-βHCG) in human serum sample, which’s suitable for auxiliary evaluation of the risk for women to carry a child with trisomy 21 (Down syndrome) in the first 3 months of pregnancy. This kit only provides free β-subunit of human chorionic gonadotropin test results, and results obtained shall be used in combination with other clinical information for analysis. It must only be used by healthcare professionals.
Summary
F-βHCG is a glycoprotein consists of α and β subunits, which accounts for around 1%-8% of total amount of HCG in mother’s blood. The protein's secreted by trophoblast in placenta, and it's very exnsitive to chromosomal abnormalities. F-βHCG is the most commonly used serological indicator for clinical diagnosis of Down syndrome. In the first 3 months of pregnancy (8 to 14 weeks), women with increased risk of carrying a child with Down syndrome can be also identified through combined use of F-βHCG, pregnancy associated plasma protein-A (PAPP-A) and nuchal translucency (NT) ultrasound.
Feature:
• High sensitive
• result reading in 15 minutes
• Easy operation
• Factory direct price
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