Polypeptide for promoting generation of African swine fever virus antigen specific immune response in swine body and application thereof
一种非洲猪瘟病毒、免疫应答的技术,应用在生物医学领域,能够解决尚未见报道等问题,达到促进免疫应答、促进致敏免疫细胞增殖的效果
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Embodiment 1
[0056] Solid phase synthesis and purity detection of embodiment 1 polypeptide
[0057] The polypeptide of the present invention is as follows:
[0058] SEQ ID NO.1: SASAINFLL, AP1;
[0059] SEQ ID NO.2: RALKYYQFL, AP2;
[0060] SEQ ID NO.3: YTLLFNHHI, AP3;
[0061] SEQ ID NO.4: SPVMKWEYVDLL, AP4;
[0062] SEQ ID NO.5: YGVEQTHIWPL, AP5;
[0063] The above polypeptides were synthesized by Shanghai Sangon Biological Co., Ltd. The detection wavelength is 214nm. The purity of the final peptide purification product was >98%, and the structure was identified by ESI-MS. The identification results are shown in Figure 1~ Figure 5 ,in figure 1 is the identification chromatogram of AP1, figure 2 is the identification chromatogram of AP2, image 3 is the identification chromatogram of AP3, Figure 4 It is the identification chromatogram of AP4, and the peak time is 14.47min; Figure 5 It is the identification chromatogram of AP5, and the peak time is 12.65min. Depend on Fi...
Embodiment 2
[0064] Embodiment 2 porcine lymphocyte proliferation experiment
[0065] 1. Pigs immunized with inactivated ASFV virus.
[0066] Inactivate the virus with the ASFV popular strain (from the African swine fever regional laboratory of the Lanzhou Veterinary Research Institute of the Chinese Academy of Agricultural Sciences,) (10HID 50 ) immunized five 90-day-old male Landrace pigs, boosted the immunization once a month later, euthanized the pigs 7 days later, and took out the spleen after dissection. Unimmunized healthy pigs were used as negative control group.
[0067] 2. Preparation, culture and proliferation detection of splenocytes.
[0068] 1) Aseptically treat the collected pig spleen with 75% alcohol, wash it three times with PBS, cut the spleen into small pieces, place them in folded sterile gauze (2 layers), and place them in 5 mL of serum-containing 1640 medium Grind the spleen in a plate.
[0069] 2) Then draw the liquid into a 15ml centrifuge tube, centrifuge at 1...
Embodiment 3
[0078] Example 3 Detection of IFN-γ secretion by different subtypes of splenic lymphocytes
[0079] The pig immunization procedure and spleen cell isolation and culture are the same as in Example 2. After obtaining the dispersed splenocytes, prepare a single cell suspension with RPMI1640 complete medium at a concentration of 1×10 6 / ml. Inoculate into a 24-well plate, add 0.2 μg of the polypeptide (AP1-AP5) provided by the present invention to each well, and place in CO 2 Cultivate in the incubator for 60h. Collect the cells in each well, label the cells with porcine CD3, CD4, CD8 and IFN-γ specific antibodies respectively, then wash twice with PBS buffer containing 2% serum, and finally use the washing solution to disperse into a cell suspension, and use the flow Cytometer detection, respectively determine B lymphocytes, CD4 + T lymphocytes, CD8 + T lymphocytes, CD4 + CD8 + The levels of IFN-γ secreted by T lymphocytes and monocyte-macrophages.
[0080] For test resul...
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