Rabies antibody gold immunochromatography assay testing indicator paper and preparation technique
A technology for immunochromatographic detection and rabies virus, which is applied to measurement devices, analytical materials, instruments, etc., can solve the problem of no simple and fast detection, etc., and achieve the effects of easy operation, simple preparation method, and easy interpretation.
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Embodiment 1
[0026] 1. Preparation of goat-anti-dog IgG: Goat-anti-dog IgG made by immunizing sheep with purified canine immunoglobulin as an antigen, and the antibody is only directed against canine immunoglobulin. Use this antibody to mark colloidal gold to make gold-labeled antibody, which can combine with canine immunoglobulin in the sample to be tested, so use this antibody to mark colloidal gold and spray it on the binding pad.
[0027] 2. Preparation of rabbit anti-goat IgG: This antibody is made by immunizing rabbits with sheep immunoglobulin as an antigen, and extracting the antibody globulin in the immune rabbit serum. Used on the quality control line of the NC membrane, it can be combined with the gold-labeled antibody to detect the validity of the test strip.
[0028] 3. Preparation of rabies virus antigen: use attenuated ERA strain of rabies virus vaccine to infect monolayer Vero cells, collect the supernatant after lesion as the first-generation virus, and then infect monolay...
Embodiment 2
[0030] The production process of test strips:
[0031] 1. Preparation of sheep anti-canine IgG gold-labeled antibody (1) Preparation of colloidal gold: take concentration of 0.01% chloroauric acid (HAuCl 4) solution 100mL heating and boiling, quickly add a certain amount of 1% trisodium citrate aqueous solution, and then keep boiling for 10-15min, the colloidal gold solution with a gold particle size of 20 nanometers can be obtained; (2) colloidal gold-labeled sheep anti-canine IgG : Use 0.1M potassium carbonate (K 2 CO 3 ) solution to adjust the pH to 8.2, add goat anti-canine IgG at 2-18ug / ml, after mixing and stirring, add bovine serum albumin (BSA) at 1g / 100ml to the solution, and let stand at 4°C for 2-4 hours. The above colloidal gold solution was centrifuged at 2000r / min for 20 minutes, and the precipitate was removed to obtain the supernatant. Then the supernatant was centrifuged at 10,000 r / min for 40 minutes to obtain a precipitate. Resuspend the precipitate with...
Embodiment 3
[0037] (1) The bonding pad is made of glass fiber membrane, which is produced by Millipore Company of the United States. The bonding pad is treated with 10mMpH8.2 PBS+3%BSA+0.1%Triton X-100+1%PVP-40000 pretreatment solution and soaked for 30 minutes Afterwards, vacuum-dry at 37°C, spray colloidal gold-labeled goat anti-dog IgG and then dry. The upper part of the binding pad is connected with the sample pad, and the lower part is connected with the NC membrane;
[0038] (2) NC membrane is a kind of material specially used in the preparation of colloidal gold test strips. It is produced by Millipore Company of the United States. Two lines are sprayed on the NC membrane, and one is a detection line (purified rabies virus antigen or antigen expressed by genetic engineering) ), the other line is a quality control line (rabbit anti-goat IgG), the NC membrane is pasted in the middle of the backing, and the two ends are respectively connected with the binding pad and the water-absorbin...
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