Immunofluorescent quantitative test strip for detecting myohemoglobin
A technique of myoglobin and immunofluorescence, which is applied in the field of immunological detection, can solve the problems of long enzyme-linked immunoassay assay period, expensive instruments required for detection, and high cost of chemiluminescence, and achieve high sensitivity, good stability, and high-level Analyze the effect of recovery rate
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Embodiment 1
[0024] Embodiment 1 storage solution formula and preparation method thereof
[0025] A preferred formulation of the storage solution of the present invention: the mass concentration of PB is 20mM, the percentage concentration of BSA is 1.8%, the percentage concentration of Tween-80 is 0.5%, the percentage concentration of glucose is 0.5%, and the percentage concentration of glycine The percentage concentration of PEG4000 is 1%, the percentage concentration of PEG20000 is 1.5%, the percentage concentration of Proclin300 or sodium azide is 0.03%, and the pH is 7.5.
[0026] Preparation method of storage solution: Weigh 0.25g of glucose and dissolve it in 45mL of pure water. Add 1mL of 100mM PB stock solution prepared in advance, shake and mix well. Add 1g of glycine, 0.5g of PEG4000, 0.75g of PEG20000 and 0.9g of BSA successively, shake and mix well; add 0.25mL Tween-80 with a sample gun, mix well repeatedly; add 15μL of Proclin300, shake and mix well; adjust the pH to 7.5 with...
Embodiment 2
[0028] The preparation method of embodiment 2 myoglobin immunofluorescence quantitative test strip
[0029] The preparation process of the myoglobin immunofluorescence quantitative test strip is as follows:
[0030] (1) Preparation of storage solution: the mass concentration of PB is 20mM, the percentage concentration of BSA is 1.8%, the percentage concentration of Tween-80 is 0.5%, the percentage concentration of glucose is 0.5%, and the percentage concentration of glycine is 2%, the percentage concentration of PEG4000 is 1%, the percentage concentration of PEG20000 is 1.5%, the percentage concentration of Proclin300 is 0.03%, and the pH7.5 is prepared according to the above formula, mixed and then filtered and sterilized to obtain a storage solution;
[0031] (2) Preparation of the sample pad: soak the glass fiber membrane with the sample pad treatment solution for 10 minutes, place in a drying room at 37°C and 30% humidity, and dry for 3 hours to prepare the sample pad for ...
Embodiment 3
[0046] Prepare the control storage solution, the specific formula is: the mass concentration of PB is 50mM, the percentage concentration of BSA is 1%, the percentage concentration of Tween-80 is 1%, the percentage concentration of glucose is 1%, the percentage concentration of glycine 0.5%, the percentage concentration of PEG4000 is 2%, and the percentage concentration of Proclin300 is 0.3%.
[0047] The preferred storage solution prepared in Example 1 (hereinafter referred to as storage solution 2) is compared with the reference storage solution (hereinafter referred to as storage solution 1) for stabilizing performance and precision, and the implementation method and results are as follows:
[0048] Using storage solution 1 and storage solution 2, the fluorescent microspheres labeled with myoglobin (MYO) monoclonal antibody by the same process were sprayed and dried, assembled into 40 test strips, put in aluminum foil bags, and sealed with desiccant. One bag was stored in re...
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