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  • Ebola Antigen Rapid Test
  • Ebola Antigen Rapid Test

Ebola Antigen Rapid Test

Usage
The Ebola Antigen Rapid Test is a rapid, serological, lateral flow chromatographic immunoassay for the qualitative detection of antigens from Ebolaviruses in human whole blood, serum or plasma specimens as an aid in the diagnosis of Ebola virus infection.

 

Background of Clinical Indications

First symptoms are the sudden onset of fever fatigue, muscle pain, headache and sore throat. This is followed by vomiting, diarrhoea, rash, symptoms of impaired kidney and liver function, and in some cases, both internal and external bleeding (e.g., oozing from the gums, blood in the stools). Laboratory findings include low white blood cell and platelet counts and elevated liver enzymes.

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Packing specification

Principle of Inspection

The Ebola Antigen Rapid Test is a qualitative membrane-based immunoassay for the detection of antigens from Ebola viruses in human whole blood, serum or plasma specimens. After specimen is added to the specimen well (S) on the sample pad, it moves through the conjugate pad and mobilizes gold anti-Ebola conjugate that is coated on the conjugate pad. The mixture moves along the membrane by capillary action and reacts with anti-Ebola antibody that is coated on the test line region (T). If the specimen contains Ebola virus antigen, a colored line will appear in the test line region (T), indicating a positive result. If the specimen does not contain Ebola virus antigen, a colored line will not appear in this region, indicating a negative result. An internal quality control is included in the test, in the form of a colored line appearing in the control line region (C), indicating that the test is functional, and proper and sufficient volume of specimen has been applied to enable migration through the test and control line, regardless of whether there is a test line or not. If the control line (C) does not appear within the testing time, test result is invalid and the test should be repeated with a new test device.

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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