Preparation method of signal-enhancement type immunochromatographic gold-labeled test strip
A gold standard test paper, signal enhancement technology, applied in the direction of analysis materials, measuring devices, instruments, etc., can solve the problems that large instruments cannot be popularized and used, large instruments are expensive, and detection costs are expensive, achieving high specificity, low cost, good stability effect
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Embodiment 1
[0033] A method for preparing a signal-enhanced bisphenol A immunochromatographic gold standard test strip. The specific steps are as follows:
[0034] (1) Preparation of rabbit anti-bisphenol A gold-labeled immunoprobe
[0035] A colloidal gold solution with a particle size of 40nm was selected, and potassium carbonate (K 2 CO 3 ) solution to adjust the pH value of the colloidal gold solution to 8.5 to obtain the adjusted colloidal gold solution A;
[0036] Mix the rabbit anti-bisphenol A antibody solution with a concentration of 1 mg / mL and the bovine serum albumin (BSA) solution with a concentration of 1 mg / mL at a molar ratio of 1:100 to obtain a mixed solution;
[0037] Take 10 μL of the mixed solution and add it to 1 mL of the adjusted colloidal gold solution A, and shake it at room temperature for 15 minutes;
[0038] Centrifuge at 10,000 rpm for 20 min at 4°C to remove unbound antibodies and bovine serum albumin (BSA) in the supernatant;
[0039] The precipitate ob...
Embodiment 2
[0051] A method for preparing a signal-enhanced phthalate immunochromatographic gold standard test strip. The specific steps are as follows:
[0052] (1) Preparation of rabbit anti-phthalate gold-labeled immunoprobe
[0053] Select a colloidal gold solution with a particle size of 30nm, adjust the pH value of the colloidal gold solution to 9.5 with a potassium carbonate (K2CO3) solution with a concentration of 0.1 M, and obtain the adjusted colloidal gold solution A;
[0054] Mix the rabbit anti-phthalate antibody solution with a concentration of 2 mg / mL and the bovine serum albumin (BSA) solution with a concentration of 2 mg / mL at a molar ratio of 1:100 to obtain a mixed solution;
[0055] Take 10 μL of the mixed solution and add it to 1 mL of the adjusted colloidal gold solution A, and shake it at room temperature for 15 minutes;
[0056] Centrifuge at 10,000 rpm for 20 min at 4°C to remove unbound antibodies and bovine serum albumin (BSA) in the supernatant;
[0057] The ...
Embodiment 3
[0069] A preparation method of a signal-enhanced rabbit anti-lycodopamine immunochromatographic gold standard test strip The specific operation steps are as follows:
[0070] (1) Preparation of rabbit anti-lycodopamine gold-labeled immune probe
[0071] A colloidal gold solution with a particle size of 30nm was selected, and potassium carbonate (K 2 CO 3 ) solution to adjust the pH value of the colloidal gold solution to 9.5 to obtain the adjusted colloidal gold solution A;
[0072] Mix the rabbit anti-lycodopamine antibody solution with a concentration of 2 mg / mL and the bovine serum albumin (BSA) solution with a concentration of 2 mg / mL at a molar ratio of 1:100 to obtain a mixed solution;
[0073] Take 10 μL of the mixed solution and add it to 1 mL of the adjusted colloidal gold solution A, and shake it at room temperature for 15 minutes;
[0074] Centrifuge at 10,000 rpm for 20 min at 4°C to remove unbound antibodies and bovine serum albumin (BSA) in the supernatant;
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