Colloidal gold immunochromatographic test strip for detecting in-vivo neutralizing antibody after injection of novel coronavirus vaccine and preparation method of colloidal gold immunochromatographic test strip
A technology of immunochromatography test paper and colloidal gold, which is applied in the direction of immunoassay, biological test, measuring device, etc., to achieve the effects of lower detection limit, stable combination, and small batch-to-batch difference
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Embodiment 1
[0056] Embodiment 1: the preparation of colloidal gold immunochromatography test strip
[0057] The colloidal gold immunochromatographic test strip is prepared according to the following method, and its structure is as follows: figure 1 Shown:
[0058] Paste the sample pad 1, the colloidal gold pad 2, the nitrocellulose membrane 3 and the absorbent filter paper 6 on the polyvinyl chloride (PVC) base plate 7 from left to right, and then place the PVC base plate 7 and the attached materials Cut into test strips with a width of 3mm, and put them into a card case, which is provided with a sample loading area and a color developing area (observation area).
[0059] Among them, sample pad 1 is a glass fiber membrane; colloidal gold pad 2 is coated with colloidal gold-labeled recombinant new coronavirus RBD protein; nitrocellulose membrane 8 is coated with angiotensin converting enzyme 2 (ACE2) detection line 4 , also coated with mouse anti-chicken IgG antibody as quality control l...
Embodiment 2
[0060] Example 2: Antibody coating
[0061] First, dilute the mouse anti-chicken IgG antibody and angiotensin-converting enzyme 2 (ACE2) with coating buffer 0.05mol / L PB with a pH of 7.2-7.4 to obtain the detection line 4 mouse anti-chicken IgG antibody coating solution and quality control Line 5 Angiotensin Converting Enzyme 2 (ACE2) Diluent;
[0062] Secondly, draw the obtained dilution onto the nitrocellulose membrane using a gold-spray film marking device, and draw the line at a condition of 0.1 μL / cm;
[0063] Finally, the nitrocellulose membrane was dried in an oven at 37°C for 3 hours, and sealed with a desiccant after drying;
Embodiment 3
[0064] Embodiment 3: the preparation of colloidal gold pad
[0065] (1) Wash the utensils, adjust the pH value of the colloidal gold particles to 8.5 with potassium nitrate, add them to the utensils, then add PEG6000 separating agent with a final concentration of 10%, and then add the recombinant novel coronavirus RBD protein to a final concentration of 30 μg / ml, stirred for 40min to obtain a colloidal gold solution;
[0066] (2) Add 10% BSA blocking solution to the colloidal gold solution obtained in step (1) to a final concentration of 1% for blocking for 15 minutes;
[0067] (3) Centrifuge the colloidal gold solution obtained in step (2) at 4°C and 12,000 rpm for 40 minutes, remove the supernatant after centrifugation, and redissolve the precipitate with a reconstitution solution to obtain a recombinant novel coronavirus RBD protein labeling solution;
[0068] The complex solution is a mixture of Tween 20 and BSA;
[0069] (4) Spray the recombinant 2019-nCoV RBD protein ...
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