Rapid joint test strip for avian reticuloendotheliosis virus and subgroup j avian leukosis virus
An avian leukemia virus and avian reticuloendothelial technology, which is applied in the field of instruments for detecting avian reticuloendothelial hyperplasia and avian leukemia in subgroup J, can solve the problems of being difficult to be suitable for the production line for rapid differential diagnosis, complicated test operations and high operational requirements. , to achieve the effect of intuitive display, strong detection specificity and high sensitivity
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Embodiment 1
[0029] Example 1: A test strip for rapid detection of avian reticuloendotheliosis virus REV and J subgroup avian leukosis virus ALV-J by one-step method, see figure 1 , figure 2 . The support layer 1 is made of plastic thin strips, the sample adsorption fiber layer 2 is made of glass wool, and the gold-labeled antibody fiber layer 3 is glass wool with colloidal gold-labeled anti-REV and anti-ALV-J monoclonal antibodies The prepared mixed gold-labeled antibody, the cellulose membrane layer 4 is made of nitrocellulose, and the water-absorbing layer 5 is made of water-absorbing filter paper. The layers numbered 2, 3, 4, and 5 are pasted on the support layer 1 in sequence, and spliced together The fibers at the junction cross-penetrate each other. On the cellulose membrane layer 4, two kinds of anti-REV and anti-ALV-J polyclonal antibody IgG solutions are respectively labeled REV detection blot 6-1 and ALV-J detection blot 6-2 (codes are respectively T1 and T2) , and the c...
Embodiment 2
[0051] Example 2: The rapid detection test strip of poultry reticuloendotheliosis virus and J subgroup avian leukosis virus, its structure, preparation method are basically the same as embodiment 1, and difference is:
[0052] Colloidal gold-labeled anti-REV and anti-ALV-J mixed gold-labeled polyclonal antibodies are attached to the gold-labeled antibody fiber layer 3 made of nylon fibers; Detection blots T1 and T2 sprayed with anti-REV and anti-ALV-J monoclonal antibody IgG solutions, control blot C sprayed with goat (rabbit) anti-mouse IgG solution. Others including test sample preparation, operation method and result judgment are the same as in Example 1 and will not be repeated.
Embodiment 3
[0053] Example 3: The rapid detection test strip of poultry reticuloendotheliosis virus and J subgroup avian leukosis virus, its structure, preparation method are basically the same as embodiment 1, and difference is:
[0054] The gold-labeled antibody fiber layer 3 made of polyester fibers is attached with anti-REV and anti-ALV-J mixed gold-labeled monoclonal antibodies; on the cellulose film layer 4 made of polyvinylidene fluoride, the following Detection blots T1 and T2 sprayed with anti-REV and anti-ALV-J polyclonal antibody IgG solutions, control blot C sprayed with goat (rabbit) anti-mouse IgG solution.
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