幽门螺杆菌
Copyright ©The Author(s) 2004.
世界华人消化杂志. 2004-05-15; 12(5): 1096-1099
在线出版 2004-05-15. doi: 10.11569/wcjd.v12.i5.1096
图1
图1 带有接头的v基因片段的PCR扩增. 1: DNA marker; 2: PCR product; 3: control.
图2
图2 重组质粒pTrc99A-V-HpaA限制性酶切分析. 1: pTrc99A-HpaA /Ncoa+EcoRa; 2: pTrc99A-V-HpaA /Ncoa+ BamHⅠ; 3: pTrc99A-V-HpaA / Ncoa+EcoRa; 4: DNA marker.
图3
图3 融合基因v-hpaA 的PCR扩增. 1: DNA marker; 2-4: PCR product; 5: control.
图4
图4 重组质粒pQE-30-hpa-vacA限制性酶切分析. 1: pQE30-V-HpaA / BamHⅠ+ SalI; 2: pQE30-V-HpaA / EcoRa+ BamHI; 3: pQE30 / BamHⅠ+ SalI; 4; DNA marker.
图5
图5 DH5a/pQE30-V-HpaA表达产物SDS-PAGE鉴定结果. 1: protein marker; 2: DH5a/pQE30 induced with IPTG; 3: DH5a/ pQE30-V-HpaA induced without IPTG; 4-8: DH5a/pQE30-V-HpaA induced with IPTG.
图6
图6 融合蛋白的Western blotting鉴定结果. 1: Protein marker; 2: Noninduced protein exhibited with anti-serum against H. pylori Ab-HRP; 3-4: induced protein exhibited with anti-serum against H. pylori Ab-HRP.

引文著录: 刘淼, 杨致邦, 林珊珊, 吴利先. 幽门螺杆菌vacA毒性片段与hpaA融合基因的原核表达. 世界华人消化杂志 2004; 12(5): 1096-1099