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  • Zika NS1 Antigen Rapid Test
  • Zika NS1 Antigen Rapid Test

Zika NS1 Antigen Rapid Test

Usage
The Zika NS1 Antigen Rapid Test is a rapid test for the qualitative detection of NS1 antigen of Zika virus in human whole blood, serum or plasma specimens to assist in the diagnosis of Zika infections. The test only provides preliminary analysis results but not critical diagnosis criteria. Any use or interpretation of the test must be analyzed and confirmed with alternative testing method(s) and clinical findings based on professional judgment of healthcare providers.
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Packing specification

Principle of Inspection

The Zika NS1 Antigen Rapid Test is a qualitative membrane-based immunoassay for the detection of Zika NS1 antigen in whole blood, serum, or plasma. During the test procedure, capture reagent is immobilized in the test line region (T) of the test. After specimen is added to the specimen well (S) of the device, the specimen reacts with Zika NS1 antibody-conjugate in the test cassette. The Gold antibody conjugate will bind to Zika NS1 antigen in the specimen sample which in turn will bind with Anti-Zika NS1 coated on the membrane. As the reagent moves across the membrane, the Zika NS1 antibody on the membrane will bind the antibody-antigen complex causing a dark red or pink line to form at the test line region of the test membrane. The intensity of the lines will vary depending upon the amount of antigen present in the sample. If the specimen contains Zika NS1 antigen, a colored line will appear in the test line region (T), indicating a positive result. If the specimen does not contain Zika NS1 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

1 Test/Kit, 2 Tests/Kit, 5 Tests/Kit, 7 Tests/Kit, 10 Tests/Kit, 20 Tests/Kit, 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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