Fluorescent microsphere detection device for gastric function and gastric cancer risk and preparation method thereof
A technology of fluorescent microspheres and detection devices, which can be used in measuring devices, biological testing, material inspection products, etc. It can solve the problems of easy quenching of fluorescent antibodies, insufficient amount of protein adsorbed by NC membranes, and weak binding force, etc., to improve sensitivity , Accurate early warning and disease risk judgment, the effect of reducing dosage
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Embodiment 1
[0044] The sample pad 1, the immunofluorescent antibody glass fiber membrane 2, the nitrocellulose membrane 3, and the absorbent pad 4 are respectively pasted on the plastic plate 5, and the two ends of the nitrocellulose membrane 3 are connected to the absorbent pad 4, the immunofluorescent antibody glass fiber membrane, respectively. 2 overlapping, the other end of the immunofluorescence antibody glass fiber membrane 2 is overlapped with the sample pad 1; the nitrocellulose membrane 3 is provided with a first detection line T1, a second detection line T2, a third detection line T3, The fourth detection line T4, the fifth detection line T5, the quality control line (C1) and the quality control line (C2); the solid phase of the first detection line T1 has a highly specific gastrin 17 antibody, and the The solid phase of the second detection line T2 has a highly specific pepsinogen I antibody, the solid phase of the third detection line T3 has a highly specific pepsinogen II ant...
Embodiment 2
[0064] Preparation of polyethylene glycol glycerin treatment solution: mixed with polyethylene glycol glycerin and polylysine (SIGMA, 150KD), wherein the concentration of polyethylene glycol glycerin is 0.5%, and polylysine The concentration is 0.5%, filtered through a 0.22μm filter membrane, and set aside;
[0065] The concentration of Tris-HCL solution is 0.1mol / L, the concentration of bovine serum albumin BSA is 0.7%, the concentration of casein is 0.15%, and the concentration of surfactant is 0.7%;
[0066] All the other are with embodiment 1.
Embodiment 3
[0068] Preparation of polyethylene glycol glycerin treatment solution: mixed with polyethylene glycol glycerin, polylysine (SIGMA, 150KD) and PEG2000, wherein the concentration of polyethylene glycol glycerin is 0.5%, poly The concentration of lysine is 0.5%, the concentration of PEG20000 is 0.1%, and it is filtered through a 0.22 μm filter membrane, and it is set aside;
[0069] The concentration of Tris-HCL solution is 0.1 mol / L, the concentration of bovine serum albumin BSA is 1%, the concentration of casein is 0.2%, and the concentration of surfactant is 1%.
[0070] All the other are with embodiment 1.
[0071] Further illustrate the effect of the present invention by experiment below.
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