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Test kit (Combi rapid test) for the synchronous identification of biomarkers in feces for the identification of pathological modifications in the gastrointestinal tract, especially in the intestine
Test kit (Combi rapid test) for the synchronous identification of biomarkers in feces for the identification of pathological modifications in the gastrointestinal tract, especially in the intestine
Test kit for the detection of biomarkers in human feces, consisting of a first test tube, which contains a first device for extracting fecal samples to collect the amount of feces necessary, a first buffer solution containing Hepes 10- buffer. 70 mM with a pH value of 7.6-8.2, a second test tube, containing a second device for collecting fecal samples to collect the required amount of feces, a second buffer solution containing acetate buffer 10 -70 mM with pH value 5-6, an assay cassette containing a lateral flow assay system with a nitrocellulose membrane stored for one to six months as stationary phase, the nitrocellulose membrane containing monoclonal tumor antibody M2- Mouse PK, that is, clone PATAM3AT, IgG1 and gold-coupled monoclonal mouse antibody, that is, clone 1 E3, IgG1, and mouse monoclonal hemoglobin antibody, that is, clone M1202100, IgG1, and monoclonal mouse antibody coupled to gold, that is, clone HB11-2312, a first hole for taking a stool sample from the first test tube, a second hole for taking a stool sample from the second test tube, the result of the analysis of the first fecal sample being positive if the content of M2-PK tumor is greater than 4 ± 1 units / ml of fecal extract, and the result of the analysis of the second fecal sample being positive if the hemoglobin content exceeds 24 μg of hemoglobin per gram of stool.
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