Chemical luminescence ELISA detection reagent kit of ciprofloxacin
A technology of chemiluminescence enzyme and ciprofloxacin, which is applied in chemiluminescence/bioluminescence, analysis by causing chemical reactions of materials, and measurement devices, can solve the problems of complex processing, long time, high detection cost, etc., and achieve sensitivity high effect
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Embodiment 1
[0021] Example 1. Preparation of immunogen, coated antigen and antibody
[0022] (1) Synthesis of immunogen
[0023] The immunogen was obtained by coupling ciprofloxacin and bovine serum albumin (BSA) by EDC method. It includes the following steps:
[0024] A. Weigh 20.0mg (54.4μmol) of ciprofloxacin, 104.2mg (544μmol) of water-soluble carbodiimide (EDC), 31.3mg (272μmol) of N-hydroxysuccinimide (NHS) and dissolve in 5mL. In DMF, keep away from light and react with magnetic stirring at room temperature for 24 hours;
[0025] B. Dissolve 123.3mg (1.8μmol) BSA (molecular weight range of 6.7KDa~6.8KDa) in 10mL phosphate buffer solution (PBS) (0.01M, pH7.4);
[0026] C, slowly add the "product of step A" to the "product of step B", and react with magnetic stirring at room temperature for 3 hours; after the reaction is completed, transfer the reaction solution to a semi-permeable membrane, and use PBS (0.01 M, pH7.4) dialysis for 3 days, during which the dialysate was changed every 4-6...
Embodiment 2
[0030] Example 2. Establishment of CL-ELISA detection method
[0031] 2.1 The optimal concentration of antibody and coating antigen (square matrix)
[0032] For each coating antigen in the longitudinal direction, serial dilutions of 40.0μg / mL, 20.0μg / mL, 10.0μg / mL, 5.0μg / mL, 2.5μg / mL, 1.25μg / mL, 0.625μg / mL, 0.3125μg / mL Degree-coated microtiter plate, 100μL / well, placed overnight at 0-4°C, wash the plate three times with washing solution, and pat dry each time; block with 250μL / well blocking solution, place at room temperature for 3 hours, wash the plate three times, pat dry each time ; Add 100μL / well of a series of diluted antibodies (1:100 to 1:1024000), place at room temperature for 2 hours, wash the plate three times, and pat dry each time; add 100μL / well of 1:1000 horseradish peroxidase labeled Goat anti-rabbit antibody, place at room temperature for 1 hour, wash the plate three times, and pat dry each time; add 100 μL / well of luminescence solution to determine the luminescenc...
Embodiment 3
[0042] Example 3. Chemiluminescence enzyme-linked immunoassay kit for detecting ciprofloxacin
[0043] (1) The composition of a chemiluminescence enzyme-linked immunosorbent assay kit for the detection of ciprofloxacin
[0044] a. Solid-phase carrier (enzyme-labeled plate) coated with coated antigen (conjugate of ciprofloxacin and carrier protein);
[0045] b. 6 bottles of ciprofloxacin standard solution with concentrations of 0.1ng / mL, 0.2ng / mL, 0.5ng / mL, 1ng / mL, 2ng / mL, 5ng / mL;
[0046] c. Ciprofloxacin antibody working solution (working concentration is 1:8000);
[0047]d. Horseradish peroxidase labeled goat anti-rabbit IgG antibody working solution (working concentration is 1:1000);
[0048] e. Concentrated phosphate buffer solution: NaCl 80.0g, KH 2 PO 4 2.0g, Na 2 HPO 4 . 12H 2 O 2 29.0g, KCl 2.0g, add double distilled water to 1000mL, pH 7.5;
[0049] f. Concentrated washing liquid: NaCl 80.0g, KH 2 PO 4 2.0g, Na 2 HPO 4 .12H 2 O 2 29.0g, KCl 2.0g, tween-200.5mL add doub...
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