HIV 1/2 Rapid Test Kit (Colloidal gold method)

HIV 1/2 Rapid Test Kit (Colloidal gold method)

Consumables
HIV 1/2 Rapid Test Kit (Colloidal gold method)
HIV 1/2 Rapid Test Kit (Colloidal gold method)

Information

This product is used for in vitro qualitative detection of human immunodeficiencyvirus antibodies (HIV 1/2) in human whole blood/serum/plasma, including type l andtype 2 antibodies. The pathogen of Acquired Immune Deficiency Syndrome (AIDS) is human immuno-deficiency virus (HIV), belongs to the genus Lentivirus of the Retroviridae family.AIDS is caused by HIV, and it can damage the body's immune system, Globally, HIV-lhas the highest prevalence, especially HIV-1 M group is the leading cause of AIDSworldwide. The HIV-2 infected population is mainly distributed in western Africancountries. Combined with clinical and other laboratory indicators, this product is usedfor the auxiliary diagnosis of human immunodeficiency virus infection. This productis suitable not only for professional medical personnel to test in medical units, but alsofor consumer self- test. HIV-1/2 antibody detection includes enzyme-linked immunosorbent assay, chemilu-minescence or immunofluorescence,immunochromatography, and western blotting
Nanjing Synthgene Medical Technology Co., Ltd.Z1.B30Nanjing Synthgene Medical Technology Co., Ltd. is a high-tech enterprise focusing on thedevelopment and production of in vitro diagnostic (lVD) materials and point-of-care testing(POCT) diagnostic reagents. The company has advanced technology platforms, includingprotein expression and purification platforms, hybridoma monoclona antibody screening plat-forms and antibody engineering design platforms, etc., which provide a solid technical founda-tion for the development of antibodies used in diagnostic assays. In addition, our company currently has fluorescence chromatography platform and latex turbidi-ty platform, We are committed to promoting the accurate diagnosis of human diseases withhigh-quality diagnostic products and contributing to the cause of human health. Synthgene's manufacturing system meets GMP standards for medical devices, and is certifiedwith ISO13485:2016 by NQAShanghai National Quality Assurance Certification Co., Ltd). Relevant in vitro diagnostic reagent products have obtained the EU CE certification. Synthgene isalso a member on the "allow list" issued by Chinese Ministry of Commerce for anti-epidemicproducts exporting POCT kits, which have been recognized by customers around the world. TEL:+86(025)83696681

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