Fluorescent brightening agent VBL detection kit and preparation method thereof
A technology of fluorescent whitening agent and detection kit, which is applied to measuring devices, instruments, scientific instruments, etc., can solve the problems of inability to identify the type of fluorescent whitening agent, high detection cost, complicated processing, etc., so as to reduce errors and detection costs. Low, simple preprocessing effect
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Embodiment 1
[0025] The main components of the fluorescent whitening agent VBL detection kit described in the present embodiment are as follows:
[0026] 1) Fluorescent whitening agent VBL specific antigen working solution;
[0027]Prepared by the following method: Disperse fluorescent whitening agent VBL0.87g, namely 1.0mmol, and triethylamine 1.01g, namely 10mmol, in 100mL dry dichloromethane, add 0.5L at zero degrees Celsius, namely 6.46mmol methanesulfonyl chloride as Activate the reagent, stir and react at room temperature for 3.5 hours, the alcoholic hydroxyl group of the fluorescent whitening agent VBL can be converted into a methylsulfonate group; then add the mesylated fluorescent whitening agent VBL to absolute ethanol, and add 20 times the amount of liquid ammonia , reflux and stir for 5 hours to prepare the hapten of the fluorescent whitening agent VBL that can be coupled with the protein; then mix it with N-hydroxysuccinamide (NHS) and carbodiimide (EDC), and then mix it with ...
Embodiment 2
[0050] Establishment of an indirect competitive ELISA method.
[0051] The competition inhibition rate of the fluorescent whitening agent 85 monoclonal antibody was detected by the indirect competition ELISA method, and the method was as follows:
[0052] 1) Coat a 96-well ELISA plate with 2 μg / mL fluorescent whitening agent VBL-specific antigen, 100 μL / well, place in a 4°C refrigerator overnight, and block with 300 μL / well blocking solution (5% skimmed milk powder) Then wash with washing liquid and pat dry;
[0053] 2) Add fluorescent whitening agent VBL standard solution (concentration: 1×10 5 μg / L, 1×10 4 μg / L, 1×10 3 μg / L, 1×10 2 μg / L, 1×10 1 μg / L, 1×10 0 μg / L) or 50 μL of sample solution, then add 50 μL of fluorescent whitening agent VBL-specific antibody working solution with a concentration of 2 μg / mL, mix well, and incubate at 37°C for 1 hour;
[0054] 3) After washing and patting dry, add horseradish peroxidase-labeled goat anti-mouse secondary antibody diluted...
Embodiment 3
[0064] Kit sensitivity, specificity, accuracy.
[0065] 1. Sensitivity determination.
[0066] A standard working curve for the detection of the fluorescent whitening agent VBL was established by using the measurement results of the indirect competition ELISA method in Example 2. Fluorescent whitening agent VBL monoclonal antibody at 1μg / L~1×10 5 Good linearity in the range of μg / L, IC 50 =857.9ng / mL, the lowest detection limit is 0.324ng / mL, and the detection range (between 20% and 80% inhibition) is 2.817ng / mL~1212.182μg / mL. The detection limit of paper and plastic products is 0.162ng / mm 2 , the detection limit of food samples is 0.162ng / g, and the detection limit of daily chemical products is 30ng / g.
[0067] 2. Determination of specificity.
[0068] The indirect competition ELISA method of Example 2 was used to measure the fluorescent whitening agent VBL structural analogues 2-hydroxyethylamino-1,3,5-triazine, 2-anilino-1,3,5-triazine, 2- Amino-4-anilino-6-hydroxyeth...
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