Immune antibody for testing residual of polyether-like antibiotic and use thereof
A technology of polyether antibiotics and immune antibodies, applied in immunoglobulin, biological testing, measuring devices, etc., can solve problems such as large consumption of organic solvents, secondary pollution of the environment, and complicated pretreatment processes
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Embodiment 1
[0019] Embodiment 1, hapten transformation
[0020] The transformation of hapten by hydrochloric acid immersion method is realized as follows: Weigh 500 mg of monensin sodium salt, dissolve it in 1 mL of double distilled water, add 5 mL of hydrochloric acid (HCl) with a concentration of 6 molar, soak for 45-50 min, fully After contact, extract with ether, and remove the ether from the extract in a vacuum oven to precipitate crystals. Prepared into monensin acid. Precipitated crystals were identified by thin-layer chromatography and infrared spectroscopy. figure 2 It is the infrared spectrogram of monensin hapten modified by hydrochloric acid immersion method.
[0021] The transformation of hapten by cation exchange method is realized as follows: Weigh 16.308g of cation exchange resin, stir and wash it with distilled water for 3 times, then add it to the chromatography column, and adjust the flow rate to 1.5mL / min; add 200mL of hydrochloric acid with a concentration of 2 mol...
Embodiment 2
[0024] Embodiment 2. Preparation of artificial immunogen or coated antigen by isobutyl chloroformate method
[0025]1. Artificial immunogen or coated antigen can be prepared in this way: Weigh 192.5mg (0.25mmol) of monensin sodium-succinic anhydride derivative and dissolve it in 2.5mL of dioxane, stir continuously at 10°C; add equimolar 47ul of tributylamine and 35ul of isobutyl chloroformate were continuously stirred at 10°C for 50min to form a mixed anhydride solution; 340mg (0.005mmol) of bovine serum albumin (BSA) was weighed and dissolved in 22mL of 0.1 molar carbonate buffer, Slowly add 22mL of dioxane and keep it at 4°C; slowly drop the mixed acid anhydride solution into the continuously stirring protein solution and react for 5h; dialyze 4 times at 4°C, subpackage, vacuum dry and freeze to prepare artificial immunogen.
[0026] Take 225mg ovalbumin (OVA) to replace the bovine serum albumin (BSA) mentioned above, ovalbumin (OVA) is dissolved in 22mL0.1 molar carbonate b...
Embodiment 3
[0029] Example 3. Preparation of immunogen and coated antigen by water-soluble carbodiimide method
[0030] Artificial immunogen and coated antigen can also be prepared in this way: weigh 160mg (0.25mmol) monensin acid and dissolve it in 2mL of a mixture of 50% (v / v) pyridine and water; weigh carbodiimide (EDC) 160mg Dissolve in 2mL water, add dropwise to monensin acid, stir for 2h while adding; weigh 340mg (0.005mmol) bovine serum albumin (BSA) and dissolve it in 8mL water, slowly add this solution dropwise to the above mixture and keep the pH at about 6.0. After the dropwise addition, place the mixed solution in a dark place at room temperature for 24 hours; place the completed solution in a dialysis bag for dialysis for 4 days. The dialysis solution is PBS solution. Prepared as an artificial immunogen.
[0031] Weigh 225mg ovalbumin (OVA) to replace the bovine serum albumin (BSA) mentioned above, dissolve ovalbumin (OVA) in 8mL water, then slowly add this solution dropwise...
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