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Cloned s-Lap Gene Coding Area, Expression and Localization of s-Lap/GFP Fusion Protein in Mammal Cells
作者姓名:SONGYi-shu  SONGZhi-yu  LIHong-jun  WuYin  BAOYong-li  TANDa-peng  LIYu-xin
作者单位:[1]InstituteofGeneticsandCytology,NortheastNormalUniversity,Changchun130024,P.R.China [2]DepartmentofUrology,theFirstHospital,JilinUniversity,Changchun130021,P.R.China [3]China-JapanUnionHospital,JilinUniversity,Changchun130023,P.R.China
基金项目:中国博士后科学基金,吉林省自然科学基金
摘    要:s-Lap is a new gene sequence from pig retinal pigment epithelial (RPE) cells, which was found and cloned in the early period of apoptosis of RPE cells damaged with visible light. We cloned the coding area sequence of the novel gene of s-Lap and constructed its recombinant eukaryotic plasmid pcDNA3.1-GFP/s-lap with the recombinant DNA technique. The expression and localization of s-lap/GFP fusion protein in CHO and B16 cell lines were studied with the instantaneously transfected pcDNA3.1-GFP/s-lap recombinant plasmid. s-Lap/GFP fusion protein can be expressed in CHO and B16 cells with a high rate expression in the nuclei.

关 键 词:S-LAP基因  编码  蛋白质  细胞  哺乳动物  色素
收稿时间:2004-10-28

Cloned s-Lap Gene Coding Area, Expression and Localizationof s-Lap/GFP Fusion Protein in Mammal Cells
SONGYi-shu SONGZhi-yu LIHong-jun WuYin BAOYong-li TANDa-peng LIYu-xin.Cloned s-Lap Gene Coding Area, Expression and Localizationof s-Lap/GFP Fusion Protein in Mammal Cells[J].Chemical Research in Chinese University,2005,21(3):298-300.
Authors:SONG Yi-shu  SONG Zhi-yu  LI Hong-jun  Wu Yin  BAO Yong-li  TAN Da-peng  LI Yu-xin
Institution:1. Institute of Genetics and Cytology, Northeast Normal University, Changchun 130024, P. R. China;
2. Department of Urology, the First Hospital, Jilin University, Changchun 130021, P. R. China;
3. China-Japan Union Hospital, Jilin University, Changchun 130023, P. R. China
Abstract:s-Lap is a new gene sequence from pig retinal pigment epithelial(RPE) cells, which was found and cloned in the early period of apoptosis of RPE cells damaged with visible light. We cloned the coding area sequence of the novel gene of s-Lap and constructed its recombinant eukaryotic plasmid pcDNA3.1-GFP/s-lap with the recombinant DNA technique. The expression and localization of s-lap/GFP fusion protein in CHO and B16 cell lines were studied with the instantaneously transfected pcDNA3.1-GFP/s-lap recombinant plasmid. s-Lap/GFP fusion protein can be expressed in CHO and B16 cells with a high rate expression in the nuclei.
Keywords:s-Lap gene  Fusion protein  Mammal cell  Expression  Localization
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