Colloidal gold semi-quantitative quick immunity diagnosis test-paper stripe
A technology of rapid immunization and test strips, applied in the direction of biological testing, material inspection products, etc., to achieve simple detection procedures, accurate and reliable results, and simple production
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specific Embodiment 2
[0009] (1) Purchasing type A and III influenza virus-specific antigen neuraminidase (NA) and hemagglutinin protein to immunize mice, and reassured to obtain mouse-derived specific monoclonal antibodies IgG1 and IgG2 against the two antigens. (2) IgG1 was selected as the gold-labeled antibody, and the sodium citrate reduction method was used to prepare and determine that the optimal size of labeled gold nanoparticles was 15 nm, and centrifuged at 7300 rpm / min for 20 minutes to prepare a stock solution. 15nm colloidal gold and labeled monoclonal antibody were used to determine the optimal amount of protein, and the pH9.0 borate buffer was used to make the labeled monoclonal antibody a gradient of 5-50Ug / ml. After adding the gold stock solution, 10% NaCl was added for stability experiments. Minutes later, centrifuge and measure OD580nm, and the protein concentration is 10ug / ml when the optical density is stable. After preparation, add PEG to make colloidal gold stable solution. ...
specific Embodiment 3
[0011] (1) Purchasing pure staphylococcal protein A (SPA) to determine the protein content (2) Using the sodium citrate reduction method to determine the size of the optimally labeled gold nanoparticle for the SPA used, centrifuged at 2000rpm / min for 30 minutes to prepare a stock solution . Use 40nm colloidal gold and SPA to determine the optimal amount of protein, use PH9.0 borate buffer to make the labeled SPA a gradient of 5-50Ug / ml, add 10% NaCl after adding gold stock solution for stability experiment, and centrifuge for 5 minutes The OD580nm was measured, and the SPA protein concentration was 4.6ug / ml when the optical density was stable. After preparation, add PEG to make colloidal gold stable solution. (3) Absorb the marked gold standard SPA with a sterile absorbent sponge with a width of 1 cm, a width of 1.5 cm, and a thickness of 0.08 cm to make a gold marker pad. In a dark environment at 4°C, blow dry slowly with nitrogen gas for use. (4) Select sterile cellulose a...
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