Blocking ELISA method for detecting cysticercosis pisiformis cyst fluid antibody of rabbit
A technique for cysticercosis lentiformis and cysticercosis, which is applied in the field of blocking ELISA to detect cystic fluid antibodies of cysticerci lentiformis in rabbits, can solve the problem that cysticercosis lentiformis has not been established, clinical detection cannot be used, and the positive coincidence rate is high. problems, to achieve the effect of increasing the income of raising rabbits, blocking the vicious biological cycle, and purifying the environment
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[0039] Preparation of hyperimmune serum (primary antibody):
[0040] (1) Immunized animals: 5 healthy female BALB / c mice aged 6 weeks.
[0041] (2) Immune antigen: cyst fluid protein with a molecular weight of 50-100kDa.
[0042] (3) Immune adjuvants: Freund's complete adjuvant and Freund's incomplete adjuvant.
[0043] (4) Immune site: subcutaneous injection at four points on the back.
[0044] (5) Immunization dose: The immune dose for each mouse for the first immunization is 50 μg. 200 μL.
[0045] (6) Immunization method:
[0046] S1. For the first immunization, dilute cyst fluid protein with sterilized PBS, then mix it with Freund's complete adjuvant at a volume ratio of 1:1, and immunize after fully emulsifying.
[0047] S2. The second immunization was carried out two weeks later, and the incomplete Freund's adjuvant was mixed with the diluted cyst fluid protein at a volume ratio of 1:1, and the immunization was carried out after fully emulsifying. After that, immun...
Embodiment 4
[0053] Establishment of a blocking ELISA method for detecting antibody in cystic fluid of rabbit cysticerci lentiformis:
[0054] (1) Determination of optimal antigen coating concentration and serum dilution
[0055] S1. Packing plate: wrap the 96-well PVC reaction plate in the order of row×column=12×8, and wrap the plate with the concentration of 1.0, 2.0, 3.0, 4.0, 5.0, 6.0 μg / mL in turn, and use the same concentration for every two rows Coating, 50 μL per well, overnight at 4°C, washed 3 times with PBST, with an interval of 5 minutes between each time;
[0056] S2. Blocking: Block with PBST blocking solution containing 5% skimmed milk powder, 200 μL per well, 37°C, block for 2-4 hours, wash with PBST 3 times, with an interval of 5 minutes;
[0057] S3. Primary antibody reaction: remove the first column, and add 50 μL of PBS to each well, then add 100 μL diluted mouse positive serum to the first well of odd-numbered rows, add 100 μL diluted mouse negative serum to the first...
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