Monoclonal antibody of human myxovirus resistance A (A-hMxA), preparation and application thereof
A monoclonal antibody and protein technology, applied in the direction of anti-enzyme immunoglobulin, biochemical equipment and methods, instruments, etc., can solve the problems of limited application range, preparation process and main technical parameters that have not been disclosed, so as to improve the detection efficiency , high affinity, high affinity effect
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Embodiment 1
[0045] Embodiment 1, preparation and purification of anti-human hMxA protein monoclonal antibody
[0046] The strategy of using the prokaryotic expression product of hMxA gene as the immunogen to immunize Balb / C mice to obtain the B cells sensitized by the immunogen, the specific operation method:
[0047] 1. Preparation of Monoclonal Antibody Immunogen
[0048] 1. Amplification of the complete open reading frame fragment of 1hMxA gene
[0049] It is very difficult to obtain purified hMxA protein directly from tissues and cells to prepare antibodies. Therefore, it is an effective method to prepare antibodies through genetic engineering expression products. Obtaining genetic engineering expression products and transferring target genes is a prerequisite.
[0050] Using type I interferon to induce human cell lines in vitro for 6-12 hours can produce a large amount of hMxA gene transcripts, and then extract the total RNA, RT-PCR amplification and construct the recombinant transf...
Embodiment 2
[0129] Main technical indicators of hybridoma cell-3C2 and its secreted antibody
[0130] 1. The main technical indicators achieved by the hybridoma cell line-3C2
[0131] 1.1 Growth indicators of hybridoma cells:
[0132] The hybridoma cell growth, growth conditions and passage conditions were comprehensively analyzed, and it was found that the hybridoma cell line and the myeloma cell line-SP2 / 0 could not only survive in 10% fetal bovine serum (provided by GIBCO and hyclone companies) product) grows well, and can also grow well in the medium of 10% calf serum provided by the above two companies after being adapted to culture;
[0133] The above-mentioned 10% calf serum medium was used to carry out the first, fifth and tenth generation growth curve analysis of the above-mentioned 3C2 cell line. The doubling time of the cells was 3-4 hours, and the growth rate of each generation was basically the same.
[0134] For cell growth curves, see figure 1 The above results show that...
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