期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
梅毒螺旋体TpN17抗原的表达及纯化
1
作者 李佳凌 余广 邹礼乐 《泸州医学院学报》 2015年第1期23-26,共4页
目的:在大肠杆菌中重组表达梅毒螺旋体Tp N17抗原,通过亲和层析方法进行纯化,获得纯度较高的Tp N17抗原,利用该抗原建立梅毒诊断血清学方法。方法:将化学合成的Tp N17基因序列,克隆到p ET 22b质粒并转化到大肠杆菌BL21菌株中进行IPTG的... 目的:在大肠杆菌中重组表达梅毒螺旋体Tp N17抗原,通过亲和层析方法进行纯化,获得纯度较高的Tp N17抗原,利用该抗原建立梅毒诊断血清学方法。方法:将化学合成的Tp N17基因序列,克隆到p ET 22b质粒并转化到大肠杆菌BL21菌株中进行IPTG的诱导表达。利用Ni2+亲和层析柱对表达抗原进行纯化。结果:对插入片段进行测序,证实该序列结果与合成序列一致,并在大肠杆菌中成功表达Tp N17抗原,通过亲和层析获得纯度较高的目的抗原。结论:本研究中构建的大肠杆菌重组表达载体可有效的表达Tp N17抗原,经纯化后的抗原,可有望进一步应用于梅毒感染的血清学检测试剂盒的研发。 展开更多
关键词 梅毒螺旋体TpN17 pet 22b表达载体 重组表达蛋白 Ni2%pLUS%亲和层析法
下载PDF
Expression of human β-subunit nerve growth factor(hNGFB) in yeast Pichia pastoris and E.coli
2
作者 Qiao Fan Hongdi Liu +1 位作者 Tong Sun Rongqiao He 《Chinese Science Bulletin》 SCIE EI CAS 1999年第6期528-533,共6页
The gene hNGFB encoding the β subunit of human nerve growth factor (hNGF) was cloned into P. pastoris secretive expression vector pHIL-S1 and E. coli expression vector pET-15b. The recombinant hNGFB vectors pSNGF and... The gene hNGFB encoding the β subunit of human nerve growth factor (hNGF) was cloned into P. pastoris secretive expression vector pHIL-S1 and E. coli expression vector pET-15b. The recombinant hNGFB vectors pSNGF and pET15b-NGF were transformed into P. pastoris host cell GS115 (Mut^+ , His^- ) and E. coli strain BL21 (DE3) respectively. Expression and secretion of hNGFB in P.pastoris was attempted under the direction of the AOX1 promoter and PHO1 signal sequence. The positive colonies growing on medium without histidine were further selected by PCR. The yield of rehNGFB in GS115 was about 14.4% of total cellular secretive protein. The secreted protein was immunological active on Western blotting with rabbit anti-mNGFB antibodies. The fusion protein yield of rehNGFB in E. coli BL21 (DE3) was about 10.3% of total cellular protein after IPTG induction. Western blot detection showed its immunological activity. 展开更多
关键词 hNCFB p. pASTORIS secretive expression vector pet-15b fusion protein.
原文传递
水稻细胞分裂氧化酶的原核表达 被引量:1
3
作者 吴云华 方玉姣 《中南民族大学学报(自然科学版)》 CAS 北大核心 2015年第4期37-40,共4页
从水稻日本晴幼叶中提取RNA,以反转产物c DNA为模板PCR扩增得到了细胞分裂素氧化酶基因(CKO),酶切连接到p ET-28a载体上,构建了重组载体p ET-28a-CKO,在大肠杆菌BL21中表达了细胞分裂素氧化酶.
关键词 细胞分裂素氧化酶 原核表达 载体pet-28a 日本晴
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部