This product is used for the qualitative determination of human immunodeficiency virus type I (HIV-1) antibodies and type II (HIV-2) antibodies in human urine samples. It is suitable for the auxiliary diagnosis of HIV infection. The test results are only for clinical reference and cannot be used alone as the basis for confirming or excluding cases. In order to achieve the purpose of diagnosis, the test results should be used in conjunction with clinical examination, medical history and other examinations. This product can be used for consumer self-test.
[Test Principle]
HIV-1/2 antibodies are found in the urine of AIDS patients. This product uses the technology of immunochromatography to qualitatively detect HIV-1/2 antibodies in human urine samples. The urine sample is dripped into the sample well and chromatographed under the capillary effect. If there is HIV-1/2 antibody in the sample, the HIV-1/2 antibody in the sample will combine with gold-labeled HIV recombinant antigen to form a gold-labeled complex. The complex continued to move forward and specifically bound to the HIV-1/2-coated recombinant antigen of the detection line, and a purple-red line appeared. If there is no HIV-1/2 antibody in the sample, the gold-labeled complex will not be formed, and it will not specifically bind to the HIV-1/2-coated recombinant antigen immobilized at the detection line during the chromatography process, so that it can be detected during the detection process. The line is not colored;
A purple-red line appears on the control line regardless of the presence or absence of HIV-1/2 antibodies in the sample.