Porcine delta coronavirus n protein monoclonal antibody and its antigenic epitope and application
A monoclonal antibody and coronavirus technology, applied in the field of bioengineering, can solve the problems of no differential diagnosis of PDCoV-specific antibodies, differential diagnosis, etc.
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Embodiment 1
[0028] Example 1 Preparation of porcine Delta coronavirus nucleoprotein (PDCoV N protein) antibody
[0029] 1. Materials and Methods
[0030] 1.1 Materials
[0031] 1.1.1 Virus strains, cells and experimental animals
[0032] PDCoV strain JS, ST cells, and SP2 / 0 cells were all preserved by the Shanghai Veterinary Research Institute of the Chinese Academy of Agricultural Sciences; 3-4-week-old female Balb / c mice were purchased from Shanghai Slack Company.
[0033] 1.1.2 Main reagents and antibodies
[0034] DMEM was purchased from Gbico, fetal bovine serum for cell culture was purchased from BI Company; complete Freund's adjuvant, incomplete Freund's adjuvant, HT, HAT, PEG2000 were purchased from Sigama-Aldrich; reverse transcription kit, protein pre-stained Marker , BCA protein quantification kit was purchased from Thermo Fisher; pCold I, pCold TF, E.coli BL21 competent cells, LA Taq Premix, In-Fiusion HD Cloning Kit, T4 Ligase were purchased from Takara Company; Ni-NTA was...
Embodiment 2
[0057] Example 2 Identification of Monoclonal Antibody Epitopes
[0058] 1. Method
[0059] 1.1 Segmented amplification and cloning of PDCoV N protein
[0060]According to the above test results, the N1 gene after the PDCoV N protein segmentation was continued to be further truncated and segmented, and the N1 segment was divided into three overlapping small segments, each segment was named N1-1, N1 -2, N1-3. Corresponding homologous recombination primers were designed for each fragment (see Table 1 for the length and primer sequence of each fragment). XhoI and EcoR I restriction sites were introduced, respectively. Then use the primer pairs for each truncated fragment, and use the N gene of PDCoV as a template to perform PCR amplification on each segmented gene. The PCR reaction system is 50 μL, including: 25 μL LA Taq Premix, 22 μL ddH2O, above, 1 μL of downstream primers, 1 μL of cDNA template. The reaction program of PCR amplification is: pre-denaturation at 95°C for 5...
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