A test strip for detection of ev71 virus iga antibody
An antibody detection and test strip technology, applied in the field of medical testing, can solve the problems of expensive fluorescence detectors and cannot be promoted, and achieve the effect of avoiding spread and shortening the course of disease.
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Embodiment 1
[0025] Embodiment 1: Preparation of diagnostic test strip coating
[0026] The amino acid sequence of the EV71 virus VP2 protein antigen polypeptide is shown in SEQ ID NO.1. The invention adopts the bifunctional agent maleimido succinimidyl benzoate (MBS) to couple the BSA protein to the EV71 virus VP2 protein antigen polypeptide, and the coupler can be used for coating diagnostic test strips. 3 mg of MBS was weighed and dissolved in dimethylamide (DMF) to prepare an MBS solution with a concentration of 10 mM. Dissolve 3 mg of BSA in 1 ml of 10 mM PBS (pH 7.2), add 100 ul of 10 mM MBS solution, and stir magnetically at room temperature for 10-30 min to obtain a BSA / MBS solution. Purify the BSA / MBS solution with a sepharose G25 chromatography column, use 50 mM PBS (pH6.0) to equilibrate the column and elute the protein, and collect the BSA / MBS protein. Dissolve 5mg of EV71 virus VP2 protein antigen polypeptide (as shown in SEQ ID NO.1) in 100uL dimethylamide (DMF), then add 1...
Embodiment 2
[0027] Example 2: Preparation of goat anti-human IgA antibody quantum dot labeling pad
[0028] Draw 30ul of water-soluble quantum dots (surface carboxyl modification), centrifuge at 6000rpm for 8min, add 100ul of 10mM PBS (pH 7.2) to dissolve. Add mass fraction 2% N-hydroxyl sulfosuccinimide and mass fraction 2% 1-(3-dimethylaminopropyl)-3-ethyl carbodiamine hydrochloride of 30ul volume in the quantum dot solution, Add 1000 ul of 5 mg / ml goat anti-human IgA antibody solution and stir at room temperature for 4 hours. After the reaction was complete, centrifuge at 6000 rpm for 8 min, and add 1% BSA solution with a mass fraction of the precipitate to block for 2 hours. Centrifuge at 6000rpm for 8min, add 10mM PBS (pH 7.2) to dissolve the precipitate, and obtain goat anti-human IgA antibody quantum dot microspheres, which are stored at 4°C for later use. Spray the goat anti-human IgA antibody quantum dot microsphere marker on the glass fiber membrane, the dilution parameter is ...
Embodiment 3
[0029] Example 3: Nitrocellulose membrane coating
[0030] Dilute the human IgA antibody and EV71 virus VP2 protein antigen polypeptide-BSA protein with coating solution, wherein the concentration of human IgA antibody is 1.5 mg / ml, and the EV71 virus VP2 protein antigen polypeptide-BSA protein concentration is 1 mg / ml. The two are evenly sprayed onto the NC membrane, wherein the human IgA antibody is sprayed onto the C (control line) position on the NC membrane, and the EV71 virus VP2 antigen polypeptide-BSA protein is sprayed onto the T (test line) position on the NC membrane. Place the sprayed NC film at a relative humidity of 20% and a temperature of 20-35°C for drying treatment for more than 12 hours, and seal the dried NC film for later use.
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