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作 者:安政雯[1] 刘宏伟[1] 贾志敏[2] 李照峰[3] Staffan Strmblad 张宏权
机构地区:[1]南方医科大学南方医院口腔科 [2]南方医科大学药学院 [3]南方医科大学南方医院口腔科广东 广州510515 [4]Karolinska Institute Department of Biosciences and Nutrition, Huddinge SE-141 57, Sweden
出 处:《南方医科大学学报》2006年第6期730-733,共4页Journal of Southern Medical University
基 金:瑞典医学会(17450);瑞典癌症基金会(050373)~~
摘 要:目的克隆PAK5-N端基因并诱导其表达,进行多克隆抗体制备,为研究其在牙胚细胞中的生物学功能奠定基础。方法根据人全长PAK5cDNA序列,设计引物;利用PCR技术,以PAK5全长cDNA为模板扩增PAK5-N端基因,将扩增产物克隆至pGEX-4T-1载体中,经EcoRI/XhoI双酶切后进行重组质粒鉴定,DNA测序。以硫代半乳糖苷诱导其在大肠杆菌BL21中表达。利用GST融合蛋白纯化系统进行蛋白纯化,通过免疫家兔制备多克隆抗体,并在牙胚细胞中进行了初步研究。结果和结论成功克隆了PAK5-N端基因,在E.coli中表达了PAK5-NT,并纯化了GST融合蛋白,制备了PAK5特异性抗体。Westernblotting表明PAK5在牙胚细胞中过度表达,为其在口腔细胞中的生物学功能研究提供了依据。Objective To clone PAK5-N terminal sequence for expression in E.coli to prepare its polyclonal antibody, and examine the role of PAK5 in dental germ cells. Methods Based on human PAK5 eDNA sequence, PCR primers were designed to amplify PAK5-N terminal sequence. The PCR product was cloned into the expression vector pGEX-4T-1 EcoRUXhoI sites, and the recombinant plasmids were identified by agarose gel electrophoresis followed by DNA sequence analysis. The recombinant plasmids were transformed into E.coli BL21 and the expression of GST-fusion protein was induced by IPTG. Glutathione-Sepharose beads were used to purify GST-fusion PAK5-N-terminal fragrnent. Anti-PAK5 polyclonal antibody was obtained in immunizing rabbits with purified GST-PAK5 N-terminal fusion protein, and the antibodies were purified by protein A beads and used for detection of PAK5 expression in dental germ cells. Results and Condusions We successfully cloned PAK5-N terminal gene fiagment, and achieved protein expression, purification and production of PAK5-NT polyclonal antibody. The results of Western blotting indicated that PAK5 can be highly expressed in the dental germ cells, suggesting that PAK5 may play an important role in biological function of dental germ cells.
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