幽门螺杆菌
Copyright ©The Author(s) 2004.
世界华人消化杂志. 2004-08-15; 12(8): 1818-1822
在线出版 2004-08-15. doi: 10.11569/wcjd.v12.i8.1818
图1
图1 MEL-HP27 hspAureB基因的PCR扩增. 1: 100 bp DNA ladder marker; 2: PCR product of hspA gene; 3: 1 kb DNA ladder marker; 4: PCR product of ureB gene.
图2
图2 重组质粒pET-HU27酶切鉴定图谱. 1: 1 kb DNA ladder marker; 2: pET-HU27 digested by EcoRI; 3: pET-HU27 digested by EcoRI、XhoI; 4: product of hspA-ureB fusion gene from pET-HU27.
图3
图3 HspA-UreB融合蛋白的SDS-PAGE分析. 1: protein marker; 2-5: BL21 with recombinant plasmid pET-HU27 induced by IPTG for 4、3、2 and 1 h; 6: BL21 with recombinant plasmid pET-HU27 uninduced for 4 h; 7: BL21 with pET30a induced for 4 h.
图4
图4 诱导3 h融合蛋白含量分析.
图5
图5 亲和层析纯化融合蛋白结果. 1: protein marker; 2-4: purified fusion protein.
图6
图6 融合蛋白的Western blot分析. 1: unpurified fusion protein; 2: purified fusion protein.

引文著录: 代丽萍, 段广才, 范清堂, 郗园林, 张荣光. 幽门螺杆菌融合蛋白HspA-UreB的表达和免疫学活性. 世界华人消化杂志 2004; 12(8): 1818-1822