Time-resolved fluorescent immunochromatographic test strip, kit and preparation method for detecting myo
An immunochromatographic test paper and time-resolved technology, which is applied in the field of medical testing, can solve the problems of affecting microprotein activity, narrow linear range, and affecting results, etc., and achieve the effects of being suitable for large-scale production, simple preparation method, and convenient clinical use
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Embodiment 1
[0039] Example 1 Time-resolved immunochromatographic test strip for detecting MYO
[0040] A time-resolved immunochromatographic test strip for detecting MYO of this embodiment includes a bottom liner, and a sample pad, a binding pad, a coating film and absorbent paper which are sequentially arranged on the bottom liner, and the binding pad is coated MYO monoclonal detection antibody (Raybiotech.) labeled with fluorescent microspheres, the coating film includes a detection zone and a control zone arranged in parallel and spaced 0.5 cm apart from each other, the detection zone is close to the binding pad, and the control zone Close to the absorbent paper, the detection area is coated with a MYO monoclonal capture antibody that recognizes a single epitope (self-produced, prepared by using well-known techniques in the art), and the control area is coated with a goat anti-mouse IgG antibody.
[0041] In this embodiment, the coating film is a nitrocellulose film of chemically cross-link...
Embodiment 2
[0048] Example 2 Time-resolved immunochromatography kit for detecting MYO
[0049] The time-resolved fluorescence immunochromatography kit for detecting MYO of this embodiment, the kit includes: the test strip, the plastic cartridge, and the buffer bag described in embodiment 1; the test strip is contained in the plastic cartridge Inside, the buffer solution bag is located at the corners of the plastic card housing, close to the sample pad of the test strip, and a round hole is left on the surface of the buffer solution bag for needling.
[0050] In this embodiment, the reagent strip is immersed in a PBS buffer containing 0.5% BSA, 0.05% Tween 20, and 0.1-1% reducing agent. The buffer solution is a 0.01-0.1% reducing agent added to the ordinary phosphate solution to reduce the free peroxidase in the specimen. The reducing agent is reduced glutathione or ascorbic acid.
[0051] When the time-resolved fluorescence immunochromatographic kit for detecting MYO of the present invention i...
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