| Literature DB >> 33385449 |
Kun Zhang1, Yan Shi2, Puzhi Xu1, Cheng Huang1, Changming Zhou1, Ping Liu1, Ruiming Hu1, Yu Zhuang1, Guyue Li1, Guoliang Hu1, Xiaoquan Guo3.
Abstract
Liver kinase B1 (LKB1) is a member of the serine/threonine kinase family, which plays an indispensable role in the organism of animals. In the current study, the chicken LKB1 protein gene was amplified by PCR based on the primers and cDNA templates. Then, the cloning vector was constructed and the target gene was cloned. After that, the target gene was inserted into the expression vector to construct the recombinant plasmid. The recombinant plasmid was transformed into BL21 (DE3) host cells and the LKB1 recombinant proteins were successfully expressed by using Isopropyl-β-D-thiogalactopyranoside (IPTG). Finally, purified LKB1 proteins were used as antigen and the rabbit-derived antiserums were collected. The antiserum titer determined by ELISA was not less than 1:128000. The results of Western blot suggested that the polyclonal antibody is highly specific to chicken LKB1 protein. Immunofluorescence indicated that the LKB1 protein is mainly expressed in the cytoplasm of liver, heart and hypothalamus cells of chicken. Our study showed that the LKB1 polyclonal antibodies produced by this method are effective and can be used to further study the role of LKB1 in the pathogenesis of chicken disease.Entities:
Keywords: Chicken; Immunofluorescence; Liver kinase B1; Prokaryotic expression; Western blot
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Year: 2020 PMID: 33385449 DOI: 10.1016/j.ijbiomac.2020.12.195
Source DB: PubMed Journal: Int J Biol Macromol ISSN: 0141-8130 Impact factor: 6.953