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血管生成抑素的原核表达及纯化
引用本文:傅赞,吴月,李艳丽,朱自路,赵翰林,陈丙莺. 血管生成抑素的原核表达及纯化[J]. 南京医科大学学报(自然科学版), 2001, 9(5): 403-405
作者姓名:傅赞  吴月  李艳丽  朱自路  赵翰林  陈丙莺
作者单位:[1]南京医科大学第一附属医院外科,江苏南京210029 [2]南京医科大学生物与分子生物学系,江苏南京210029
摘    要:目的:构建血管生成抑素(angiostatin)的原核表达载体。并转入大肠杆菌BL21中诱导表达并纯化。方法:设计引物扩增angiostatin的cDNA,然后亚克隆入原核表达载体pET32a,并转化入大肠杆菌BL21中诱导表达。结果:通过重组质粒酶切和测序分析等方法,筛选出重组阳性克隆,转化入大肠杆菌BL21中诱导表达,并纯化成功。结论:通过构建的原核表达。获得了纯化的angiostatin蛋白。

关 键 词:生长因子 血管生成抑素 原核表达 纯化 肿瘤
文章编号:1007-4368(2001)05-0403-03
修稿时间:2001-03-01

Prokaryotic Expression of Angiostatin
FU Zan,WU Yue ,LI Yan li ,ZHU Zi lu ,ZHAO Han lin,CHEN B in yin. Prokaryotic Expression of Angiostatin[J]. Acta Universitatis Medicinalis Nanjing, 2001, 9(5): 403-405
Authors:FU Zan  WU Yue   LI Yan li   ZHU Zi lu   ZHAO Han lin  CHEN B in yin
Affiliation:FU Zan,WU Yue 1,LI Yan li 1,ZHU Zi lu 1,ZHAO Han lin,CHEN B in yin 1
Abstract:Objective:To construct the expressive vecto r of angio statin and transform into E. coli BL21(DE3), to induce the expression of recombi nant angiostatin in prokaryotic system. Methods:The cDNA of Angiosta ti n was amplified by PCR, they were subcloned into vector, and transformed into th e E. coli BL21(DE3), and induced expression of recombinant angiostatin. Re sults:The recombinant clones were picked out by the restriction endonuclea se and sequence analysis. Recombinant angiostatin was highly expressed when the st rain was induced with IPTG(1 mmol/L), and angiostatin was successfully purified. Conclusion:The recombinant angiostatin can be used in further studi es.
Keywords:growth factors  angiostatin  prokaryotic expressi on
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