Determination kit for triazophos chemoluminescence immunoassay and preparation method and using method thereof
A technology of triazophos chemistry and luminescent immunity, which is applied in the direction of analytical materials, measuring devices, scientific instruments, etc., can solve the problems of high minimum detection limit of triazophos and cannot fully meet the detection requirements, and achieve the effect of high sensitivity
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specific Embodiment approach 1
[0012]Specific embodiment one: the triazophos chemiluminescent immunoassay assay kit of this embodiment consists of a triazophos standard, a solid phase carrier coated with a triazophos monoclonal antibody, and a triazophos labeled with horseradish peroxidase Hapten, chemiluminescent sensitizer, and PBST buffer solution with a pH value of 7.4 at a concentration of 0.01mol / L; the triazophos standard consists of a blank sample and a triazophos concentration from 0.01ng / mL to 2.5 ng / mL selected 6-8 values of the sample composition; chemiluminescence sensitization solution is based on the concentration of chemiluminescence substrate is 0.5mmol / L ~ 3mmol / L, the concentration of p-iodophenol is 0.1mmol / L ~ 1mmol / L, the concentration of hydrogen peroxide is 1mmol / L~10mmol / L, and the solution prepared by diluting Tris-HCl buffer solution with a concentration of 0.1mol / L and a pH value of 8.5, wherein the chemiluminescence substrate is Luminol, isoluminol, or 7-amino-6-mercaptophtha...
specific Embodiment approach 2
[0015] Embodiment 2: This embodiment is different from Embodiment 1 in that the solid phase carrier is a microporous plate, plastic beads, plastic tubes or magnetic particles. Others are the same as in the first embodiment.
specific Embodiment approach 3
[0016] Embodiment 3: The difference between this embodiment and Embodiment 1 or 2 is that the concentrations of triazophos in the standard triazophos are 7 values selected from 0.02 ng / mL to 2.4 ng / mL. Others are the same as in the first or second embodiment.
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