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  • HCG Pregnancy Rapid Test Card
  • HCG Pregnancy Rapid Test Card

HCG Pregnancy Rapid Test Card

Usage
The HCG Pregnancy Rapid Test Card is a visual, rapid chromatographic immunoassay for the qualitative detection of human chorionic gonadotropin in urine specimens to aid in the early detection of pregnancy.

 

Background of Clinical Indications

Human chorionic gonadotropin (hCG) is a glycoprotein hormone produced by the developing placenta shortly after fertilization. In normal pregnancy, hCG can be detected in both urine and serum or plasma as early as 7 to 10 days after conception.1,2,3,4 hCG levels continue to rise very rapidly, frequently exceeding 100mIU/ml by the first missed menstrual period,2,3,4 and peaking in the 100,000-200,000mIU/ml range about 10-12 weeks into pregnancy. The appearance of hCG in both the urine and serum or plasma soon after conception, and its subsequent rapid rise in concentration during early gestational growth, which enables it an excellent marker for the early detection of pregnancy. The HCG Pregnancy Rapid Test Card is a rapid test that qualitatively detects the presence of hCG in urine specimen at the sensitivity of 10mIU/ml. The test utilizes a combination of monoclonal and polyclonal antibodies to selectively detect elevated levels of hCG in urine. At the level of claimed sensitivity, the HCG Pregnancy Rapid Test Card shows no cross-reactivity interference from the structurally related glycoprotein hormones hFSH, hLH and hTSH at high physiological levels.

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Packing specification

Principle of Inspection

The HCG Pregnancy Rapid Test Card is a sandwich immunoassay. The plastic test card supports a membrane which has been coated with reagents necessary to detect the presence of hCG. The specimen is applied to the test card and reacts initially with the specific, anti-βhCG monoclonal antibody/colloidal gold conjugate on the test membrane. This mixture moves along the membrane, by capillary action, and reacts with a specific anti-hCG in the test region. If hCG is present in the specimen, the result is the formation of a colored band in the test region. If there is no hCG in the specimen, the area will remain white. The specimen continues to flow to the control region and forms a pink to purple color, indicating the test is working and the result is valid.

Specification packaging

25 Tests/Kit, 40 Tests/Kit.

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About Kangte

Zhejiang Kangte Biotechnology Co., Ltd

Zhejiang Kangte Biotechnology Co., Ltd. was established in 2001 and is located in Zhejiang Xinchang Provincial High-tech Industrial Park. It is a national high-tech enterprise integrating R&D, production and sales of in vitro diagnostic reagents. Relying on the pioneering team spirit and scientific management, the company has repeatedly won the national advanced production unit in the in vitro diagnostic industry. 

The company has GMP standard workshops, clean workshops, R&D laboratories, equipped with high-precision testing equipment and fully automatic production equipment. In order to enhance the company's overall R&D strength, it has established a good "production-study-research" cooperative relationship with many colleges and universities. The company has obtained a number of invention patents and utility model patents and has passed ISO9001, ISO14001, ISO13485, and other system certifications. The company currently has more than 100 registered products, covering biochemical, immunological, and other fields, and many of the products have reached the leading domestic level in technology. 

The company adheres to the concept of "integrity, professionalism, efficiency and innovation" to serve customers, and constantly introduces products with higher technological content to provide customers. The company will, as always, position itself in "service technology, professionalism and efficiency, and achieve customers", and work hard to jointly shape the IVD industry and continuously improve the level of human health.

 

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