Human choionic gonadotophin HCG Test (Immune Fluorescence Detection Method) HCG POCT analyzer Serum Pregnancy Portable analyzer
group namekit swab samples
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Min Order100 piece
modelHipro
payment methodL/C, D/A, D/P, Western Union, MoneyGram, T/T, Paypal
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update timeWed, 16 Mar 2022 17:49:44 GMT
Paramtents
Type Immunoassay System
Instrument classification Class II
Application Hosipital
Certificate CE ISO
Packging & Delivery
Min Order100 piece
Briefing
Human choionic gonadotophin HCG Test (Immune Fluorescence Detection Method) HCG POCT analyzer Serum Pregnancy Portable analyzer
Detailed
Human choionic gonadotophin HCG Test (Immune Fluorescence Detection Method) HCG POCT analyzer Serum Pregnancy Portable analyzer
Quick Details
Model Number |
Hipro
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Origin |
China
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Instrument classification | Class II | ||
Function | Disease Analysis | ||
Certificate | CE ISO | ||
Application | Hosipital | ||
Product Description
[Intended Use]
This product is used to determine the content of human choionic gonadotophin
(HCG) in human serum.
[Principle]
The antibody of human choionic gonadotophin is coated on the latex surface. The HCG in the sample and the antibody become to immune complexes by Latex agglutination reaction. The immune complexes will produce the phenomenon of light scattering which is proportional to the intensity of scattered light and samples of HCG levels. Using specific protein analyzer to measure the intensity of scattered light, the concentration of HCG is determined by comparing the turbidity of samples to the standard concentration.
[Storage and Validity Period]
Store at: 2~8℃
Validity Period: 1 year
[Sample Requirements]
Fasting blood collection and separation of serum as soon as possible; avoid hemolysis; store at 2~4℃ for 3 days.
[Reference Range]
<10 IU/L
Recommended that each laboratory establish its own reference range
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