Foot-and-mouth disease hybridoma cell line, monoclonal antibody, detection reagent and kit
A technology of hybridoma cell lines and monoclonal antibodies, which is applied in measuring devices, botanical equipment and methods, biochemical equipment and methods, etc., and can solve problems such as virus reactivation, poor detection efficiency, and high risk
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experiment example 1
[0052] Experimental Example 1: Materials and Methods
[0053] 1.1: Serum
[0054] To test the sensitivity of the detection, 32 serum samples of FMD-positive pigs were collected from 8-week-old pigs 34 days after the experimental challenge with FMD virus O / TAW / 97 strain.
[0055] In order to compare the sandwich ELISA detection kit provided by the present invention with other three commercially available ELISA detection kits, it was obtained from 32 head without specific pathogen (Specific-pathogen-free; SPF) and experimentally infected with foot-and-mouth disease virus A total of 320 serum samples were collected from pigs with O / TAW / 97 virus strain. The aforementioned 320 serum samples were collected at 0, 2, 4, 6, 8, 10, 14, 21, 28, and 34 days after virus infection. In addition, 30 serum samples collected from pigs 28 days after experimental infection with the FMD O / TAW / 97 strain were also tested.
[0056] To test specificity, 255 serum samples were collected from uninfec...
experiment example 2
[0077] Experimental Example 2: Expression of 3ABC recombinant protein in E. coli
[0078] The foot-and-mouth disease virus O / TAW / 993ABC gene sequence was taken from the GenBank database of the National Center for Biotechnology Information (NCBI), GenBank accession No. AJ539137, the nucleotide region of No. 5595 to No. 6119, and its detailed sequence is as SEQ ID As shown in NO: 1, it contains a coding region (Coding region) with a length of 525 nucleotides, so the encoded recombinant protein is 175 amino acids in length (the sequence is shown in SEQ ID NO: 2). Comparing the genome sequences of Pan-Asia foot-and-mouth disease virus serotype O isolated from Asia, Africa and Europe recently, the gene identity is about 97% to 99%.
[0079] The above DNA fragment amplified by reverse transcription-polymerase chain reaction was inserted into pETvector expression vector. The aforementioned expression vector was introduced into competent cells of Escherichia coli BL21DE3 strain, and ...
experiment example 3
[0081] Experimental Example 3: Mouse Immunization and Preparation of Anti-3ABC Monoclonal Antibody
[0082] The hybridoma cell line producing anti-3ABC recombinant protein monoclonal antibody was prepared by the following method: 200 micrograms of the 3ABC recombinant protein prepared in Experimental Example 1.5 was used as an antigen to immunize BALB / c mice by subcutaneous injection. The interval is 4 weeks. Three to four days before cell fusion, mice were boosted by subcutaneous injection with the same amount of antigen in phosphate buffered solution. The immunized BALB / c mice were sacrificed and their spleens were removed, and the obtained spleen cells were fused with Sp2 / 0 myeloma cells to obtain hybridoma cells. After two weeks, the culture supernatant of hybridoma cells was screened by indirect enzyme-binding immunosorbent assay containing recombinant protein of foot-and-mouth disease virus O / TAW / 97 or O / TAW / 99; The culture supernatant of hybridoma cells was screened, ...
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