Tyramine artificial antigen and antibody, and preparation methods and application thereof
An artificial antigen, tyramine hapten technology, applied in chemical instruments and methods, animal/human proteins, serum albumin and other directions, to achieve good application prospects, low cost, and high detection efficiency.
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Embodiment 1
[0052] (1) Preparation of tyramide artificial antigen
[0053] a. Preparation of cationized BSA (cBSA):
[0054] Accurately measure 20 mL of PBS, slowly add 18.0 mg of ethylenediamine (EDA) while stirring in an ice bath, and adjust the pH to 7.4 with 1 mol / L HCl; weigh 1.00 g of BSA and 56.0 mg of EDC and add them to the above solution, and react at room temperature for 2 hours; use a glass sand funnel Suction filtration, take the supernatant and put it into a dialysis bag; use 0.01mol / L PBS for continuous dialysis at 4°C for 3 days, then dry it with a vacuum freezer at -20°C, and finally store it in a -20°C refrigerator .
[0055] b. Linkage of tyramide to carrier protein cBSA:
[0056] Accurately weigh 20.0 mg cBSA into a 25 mL round bottom flask, add 4 mL of 0.01 mol / L PBS to dissolve it, accurately weigh 4.2 mg tyramine into a 5 mL small brown bottle, add 200 μL DMSO to dissolve it. Slowly add tyramine to the dissolved protein. Add 5 μL of 37% aqueous formaldehyde solu...
Embodiment 2
[0070] Use the tyramide antibody that embodiment 1 obtains to carry out immunodetection
[0071] (1) Coating: Dilute the coating antigen appropriately with the coating solution, then coat it on a 96-well microplate at 100 μL / well, and incubate overnight at 4°C or 3h at 37°C.
[0072] (2) Plate washing: add washing solution PBST, 250 μL / well, shake on the shaker for 2 minutes, discard PBST, repeat plate washing 3 times;
[0073] (3) Blocking: Add 200 μL of blocking solution to each well, block at 37°C for 1 hour, then discard the blocking solution, and wash the plate three times with PBST;
[0074] (4) Adding samples: first add 50 μL of tyramide standard solution or sample solution to each well, and then add 50 μL of antibody each. After adding the samples, perform a competitive reaction at 37°C for 1 hour, and then wash the plate 4 times with PBST;
[0075] (5) Add goat anti-rabbit HRP-labeled secondary antibody: Dilute the goat anti-rabbit HRP-labeled secondary antibody to a...
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