Colloidal gold detection card for rapidly detecting melamine and preparing method thereof
A melamine, detection card technology, applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve the problems of no large-volume sample detection, inability to achieve rapid detection, and high detection costs, and achieve low cost, rapid detection, and high detection accuracy. Effect
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[0028] A preparation method of a colloidal gold detection card for rapid detection of melamine, comprising the following steps:
[0029] (1) Coupling melamine hapten and ovalbumin by carbodiimide method to form conjugate melamine-ovalbumin as artificial antigen;
[0030] (2) hybridoma cells were hybridized and fused with immunogen-immunized mouse spleen cells and mouse myeloma cells, and a cell line capable of stably secreting anti-melamine monoclonal antibodies was screened to prepare anti-melamine monoclonal antibodies;
[0031] (3) prepare colloidal gold solution;
[0032] (4) labeling anti-melamine monoclonal antibody with prepared colloidal gold solution;
[0033] (5) Treat the nitrocellulose membrane with the prepared coating antigen and goat anti-mouse IgG;
[0034] (6) process the gold standard pad with the prepared gold standard anti-melamine monoclonal antibody;
[0035] (7) Assemble gold standard test strips.
Embodiment 1
[0038] Preparation of melamine-ovalbumin: weigh melamine, dissolve it in pyridine solution, add 10% succinic acid solution and sodium cyanoborohydride respectively, stir and react the mixture for 1 hour at room temperature, then concentrate to dryness at low temperature to obtain Hapten, take this hapten, dissolve it in N,N-dimethylformamide (DMF) solution, add 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) dropwise , after stirring and reacting for 20 minutes, the reaction solution was added dropwise to ovalbumin (OVA) solution, N-hydroxyl sulfosuccinimide (Sulfo-NHS) was added immediately, stirred overnight at room temperature, phosphate buffered saline ( PBS) dialyzed for 72 hours, freeze-dried and stored at -40°C; the ratio of the above reaction components is: melamine: succinic acid: sodium cyanoborohydride = 1000 mg: 4000 μl: 6 mg, hapten: EDC: OVA: NHS = 2000 mg : 5000mg: 10mg: 2500mg.
[0039] Preparation of melamine-bovine serum albumin conjugated antigen: Weigh...
Embodiment 2
[0046] The preparation of the melamine-ovalbumin: weigh melamine, dissolve it in pyridine solution, add 20% succinic acid solution and sodium cyanoborohydride respectively, stir and react the mixture at room temperature for 3 hours, then concentrate to dryness at low temperature, To obtain the hapten, take the hapten, dissolve it in N,N-dimethylformamide (DMF) solution, add 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) dropwise ), after stirring and reacting for 20 minutes, the reaction solution was added dropwise to the ovalbumin (OVA) solution, and N-hydroxysulfosuccinimide (Sulfo-NHS) was added immediately, stirred overnight at room temperature, and phosphate buffer saline (PBS) dialysis for 48 hours, freeze-dried and stored at -30°C; the ratio of the above reaction components is: melamine: succinic acid: sodium cyanoborohydride = 10 mg: 8000 μl: 300 mg, hapten: EDC: OVA: NHS = 10mg: 10000mg: 1000mg: 5000mg.
[0047] Preparation of the melamine-bovine serum albumin c...
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