Preparation method and application of immunosensor capable of simultaneously detecting human nuclear matrix protein and carcino-embryonic antigen with three antibodies and double channels
A nuclear matrix protein and immunosensor technology is applied in the field of preparation and application of triple-antibody dual-channel simultaneous detection of human nuclear matrix protein and carcinoembryonic antigen immunosensors, which can solve problems such as the inability to explain the disease state, and achieves the promotion of electron transfer, Improved robustness, high sensitivity and specificity of detection
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Embodiment 1
[0041] Example 1 Preparation method and application of a three-antibody dual-channel immunosensor for simultaneous detection of human nuclear matrix protein and carcinoembryonic antigen
[0042] (1) with Al2 o 3 Grind the glassy carbon electrode with a diameter of 4 mm with polishing powder, clean it with ultrapure water; add 6 μL, 1.0 mg / mL graphene oxide polyaniline chitosan hydrochloride GOPANICS-HCl dispersion to the electrode surface, and dry it at room temperature Film formation;
[0043] (2) Add 6 μL of gold nano-sol with a mass fraction of 1% dropwise, and dry at room temperature;
[0044] (3) Add 6 μL, 1 μg / mL human immunoglobulin antibody Ab(I) standard solution dropwise, 3 μL bovine serum albumin BSA solution with a mass fraction of 1%, wash with ultrapure water, and dry in a refrigerator at 4°C Dry;
[0045] (4) Add 6 μL, 1 μg / mL human immunoglobulin antigen Ag(I) standard solution dropwise, rinse with ultrapure water, and dry in a refrigerator at 4°C;
[004...
Embodiment 2
[0050] Example 2 Preparation method and application of a three-antibody dual-channel immunosensor for simultaneous detection of human nuclear matrix protein and carcinoembryonic antigen
[0051] (1) with Al 2 o 3 Grind the glassy carbon electrode with a diameter of 4 mm with polishing powder, clean it with ultrapure water; add 6 μL, 1.5 mg / mL graphene oxide polyaniline chitosan hydrochloride GOPANICS-HCl dispersion to the electrode surface, and dry it at room temperature Film formation;
[0052] (2) Add 6 μL of gold nano-sol with a mass fraction of 2% dropwise, and dry at room temperature;
[0053] (3) Add 6 μL, 3 μg / mL human immunoglobulin antibody Ab(I) standard solution dropwise, 3 μL bovine serum albumin BSA solution with a mass fraction of 3%, wash with ultrapure water, and dry in a refrigerator at 4°C Dry;
[0054] (4) Add 6 μL, 3 μg / mL human immunoglobulin antigen Ag(I) standard solution dropwise, rinse with ultrapure water, and dry in a refrigerator at 4°C;
[0...
Embodiment 3
[0059] Example 3 Preparation method and application of a three-antibody dual-channel immunosensor for simultaneous detection of human nuclear matrix protein and carcinoembryonic antigen
[0060] (1) with Al 2 o 3 Polish the glassy carbon electrode with a diameter of 4 mm, and clean it with ultrapure water; add 6 μL, 2.0 mg / mL graphene oxide polyaniline chitosan hydrochloride GOPANICS-HCl dispersion to the electrode surface, and dry it at room temperature Film formation;
[0061] (2) Add 6 μL of gold nano-sol with a mass fraction of 5% dropwise, and dry at room temperature;
[0062] (3) Add 6 μL, 5 μg / mL human immunoglobulin antibody Ab(I) standard solution dropwise, 3 μL bovine serum albumin BSA solution with a mass fraction of 5%, wash with ultrapure water, and dry in a refrigerator at 4°C Dry;
[0063] (4) Add 6 μL, 5 μg / mL human immunoglobulin antigen Ag(I) standard solution dropwise, rinse with ultrapure water, and dry in a refrigerator at 4°C;
[0064] (5) Add 6 μL...
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