A kind of anti-activated blood coagulation factor V monoclonal antibody and its preparation method and application
A monoclonal antibody and coagulation factor technology, applied in the biological field, can solve the problems of no anti-activated FV monoclonal antibody preparation report, lack of quantitative detection of activated FV and other problems, and achieve the effect of high affinity, strong specificity and good application prospects.
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Embodiment 1
[0021] Embodiment 1 Preparation of monoclonal antibody against activated FV of the present invention
[0022] 1. Screening of fully human FVa single chain antibody in phage antibody library
[0023] The FVa recombinant protein (product of HTI Company) was used as an antigen to screen the fully human phage antibody library. Dilute the FVa antigen with coating diluent (0.05mol / L sodium carbonate-sodium bicarbonate, pH 9.6) to 10ug / mL, add 100ul to each well of the ELISA plate, and place in a 4°C refrigerator for overnight coating. The blocking solution was mixed with PBST (PBS, 0.05% Tween 20) and 1% BSA, and 200ul was added to each well, and blocked for 1 hour. Wash 5 times with PBST, 3 min each time, add fully human Fab-based phage display library (from Shanghai Boyu Biotechnology Company phage display library), and incubate overnight at room temperature. Discard the liquid in the immunoplate, wash with PBST 5 times, each time for 3 minutes, and the phage tightly bound to th...
experiment example 1
[0040] Experimental example 1 Antigen-binding activity assay of the monoclonal antibody of the present invention
[0041] 1. Experimental method
[0042] The purified monoclonal antibody 1C11 prepared in Example 1 was used for gradient concentration affinity detection by ELISA method.
[0043] ELISA method: Dilute the FVa antigen with coating diluent to 1ug / mL, add 100ul of the diluted antigen to each well of the ELISA plate, and place it in a 4°C refrigerator overnight. Add 150ul of blocking solution to each well, and block at 37°C for 40min. Add 200ul of washing solution to each well and wash 3 times, each time 3min. Add the monoclonal recombinant phage to be tested and incubate at 37°C for 2h. Wash 3 times with washing solution, 3 min each time. Add goat anti-human-HRP (dilution ratio 1:2000) working solution, incubate at 37°C for 1 hour, add 200ul washing solution to each well and wash 3 times, 3 minutes each time. Add 100ul of temporarily prepared TMB substrate solut...
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