Fluorescence immunochromatography test strip capable of detecting early infection of pig trichina and production method thereof
A fluorescence immunochromatography and detection test paper technology, applied in the field of serological detection, can solve the problems of shortening the "window" period, etc., and achieve the effects of high detection specificity and sensitivity, easy results and simple operation.
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Embodiment 1
[0028] Embodiment 1, trichinosis fluorescent immunochromatography detection test strip
[0029] The fluorescent immunochromatographic test strip that can early detect Trichinella pig infection described in this embodiment comprises sample pad, binding pad, chromatographic membrane, water-absorbing pad and base plate, and described sample pad is provided with sample hole; Said binding pad Sprayed with fluorescent probes, the fluorescent probes include time-resolved fluorescent microspheres coupled with goat anti-rabbit IgG as indicator probes and time-resolved fluorescent microspheres coupled with Trichinella spiralis ES mixed antigen as capture probes, wherein the The Trichinella spiralis ES mixed antigen is composed of the ML-ESP antigen excreted by the muscle larvae of Trichinella spiralis and the iML-ESP antigen excreted by the muscle larvae excreted by the intestinal stage of Trichinella spiralis; the chromatographic membrane is provided with a detection line and a quality ...
Embodiment 2
[0030] Embodiment 2, the preparation method of the fluorescent immunochromatographic detection test strip of trichinellosis.
[0031] 1) Trichinella spiralis ES mixed antigen preparation: Trichinella spiralis muscle larvae excretion secretion ML-ESP antigen and Trichinella spiralis intestinal stage muscle larval secretion excretion secretion iML-ESP antigen were mixed according to the mass ratio of 1:1 to obtain Trichinella spiralis ES Mixed antigen; the specific method is:
[0032] ①Preparation of ML-ESP antigen from excreted secretion of Trichinella spiralis muscle larvae:
[0033] The collected Trichinella spiralis muscle larvae were washed three times with a culture solution containing penicillin (500U / mL) and streptomycin (500U / mL) (natural precipitation, each time for 20min), and then placed in a culture medium containing penicillin (250U / mL) and streptomycin (250U / mL) in the culture solution (density of 5000 / mL), 37 ° C, 10% carbon dioxide, cultured for 18-24h and then...
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