Test paper strip for rapidly distinguishing recent and long-term HIV infection states through serum HIV-1 antibody detection and preparation method thereof
A test strip and fast technology, applied in the biological field, can solve the problems of being unable to distinguish newly infected people from long-term infected people, and achieve the effects of shortened detection time, simple result interpretation, and simple operation
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Embodiment 1
[0043]A test strip for quickly distinguishing HIV recent and long-term infection status through serum HIV-1 antibody detection, such as figure 1 As shown, it includes a bottom plate 8 , a sample pad 1 arranged on the bottom plate 8 , a nitrocellulose membrane 3 and an absorbent paper 4 . The two ends of the nitrocellulose membrane 3 are overlapped with the sample pad 1 and the absorbent paper 4 respectively, and the end of the sample pad 1 close to the nitrocellulose membrane 3 is sprayed with a colloidal gold-labeled mouse anti-human IgG antibody to form a gold label layer 2 .
[0044] The nitrocellulose membrane 3 is provided with a second detection line 6 coated with one HIV recombinant antigen alone, a first detection line 5 coated with GP41 recombinant antigen BE23 and GP41 recombinant antigen BE33 mixedly, and a quality control of goat anti-mouse IgG antibody Line 7.
[0045] The test strip for quickly distinguishing HIV recent and long-term infection states, the coatin...
Embodiment 2
[0065] A test strip for quickly distinguishing HIV short-term and long-term infection status through serum HIV-1 antibody detection, the structure is the same as that of Example 1, and the preparation process of the test strip of this embodiment is as follows:
[0066] 1) Prepare the sample pad, sample pad 1 was purchased from Yingke Xinchuang (Xiamen) Technology Co., Ltd.;
[0067] 2) Combine mouse anti-human IgG with colloidal gold particles to form colloidal gold-labeled mouse anti-human IgG antibody, evenly spread on the gold label pad, 42ml / sheet, freeze-dry at 45°C, and set aside;
[0068] 3) Prepare the second detection line, the first detection line and the quality control line, and then put the whole at 25°C and humidity 10 ~ Under the condition of 30%, dry or dry for 18-22h;
[0069] The specific process of preparing the second detection line is: the HIV-1 recombinant antigen is diluted to a working concentration of 2.5-3.5mg / ml with coating buffer, and the second d...
Embodiment 3
[0083] The test results of Example 2 prove that the coated GP41 mixed protein will have a weak reaction with HIV recently infected serum antibodies, resulting in weak color development. This example provides different test strips.
[0084] 1) In this test example, the first detection line GP41 fusion protein was coated with BE23 and BE33 mixture. Among them, BE230.3mg / ml and BE330.45mg / ml are mixed according to the ratio of 1:1, 1:2, 1:3, 3:1, 2:1.
[0085] 2) The method of spraying gold particles and assembling test strips in this test example is the same as that of test example 1.
[0086] 3) The preparation method of the test strip of this test example is the same as that of Test Example 1.
[0087] 4) The sample loading method of this test example is the same as that of test example 1.
[0088] 5) The test result judgment method of this test example is the same as that of test example 1.
[0089] 6) We use the test results of the test kit for distinguishing short-term a...
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