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与基底细胞癌细胞凋亡相关的分子生物学研究--促凋亡分子Bad的克隆及其pEGFP-C3真核表达载体的构建
引用本文:胡彬,封兴华,刘芳.与基底细胞癌细胞凋亡相关的分子生物学研究--促凋亡分子Bad的克隆及其pEGFP-C3真核表达载体的构建[J].中国美容医学,2006,15(3):244-246,i0001.
作者姓名:胡彬  封兴华  刘芳
作者单位:1. 第四军医大学口腔医学院口腔颌面外科,陕西,西安,710032
2. 解放军空军总医院检验科
摘    要:目的:克隆Bcl-2相关凋亡基因Bad并构建其真核表达载体,探讨其对肿瘤细胞凋亡的诱导作用。方法:采用RT-PCR的方法,扩增Bad基因全长片段。通过基因定向克隆,构建Bad基因的真核表达质粒载体。结果:经酶切鉴定、PCR及DNA序列测定鉴定,Bad基因表达质粒pEGFP-C3载体成功构建。结论:成功克隆Bcl-2相关促凋亡基因Bad并构建其真核表达载体pEGFP-C3-Bad,为进一步研究Bad在人肿瘤细胞系中的促凋亡作用奠定了实验基础。

关 键 词:人Bad基因  克隆  绿色荧光蛋白  真核表达载体  基底细胞癌
文章编号:1008-6455(2006)03-0244-03
收稿时间:2005-11-11
修稿时间:2006-01-17

Cloning of human Bad gene and construction of its eukaryotic green fluorescent protein expression vector
HU Bin,FENG Xing-hua,LIU Fang.Cloning of human Bad gene and construction of its eukaryotic green fluorescent protein expression vector[J].Chinese Journal of Aesthetic Medicine,2006,15(3):244-246,i0001.
Authors:HU Bin  FENG Xing-hua  LIU Fang
Abstract:Objective To explore the expression of the truncated Bad gene and its pro-apoptotic effect on BCC(basal cell carcinoma ) cells. Methods A full-length human bad gene was cloned by RT-PCR and confirmed by sequence analysis.By deleting the 60 amino acids of N-ter-minal the truncated bad(tbad)gene was attained and then inserted into the eukaryotic expression vector pEGFP-C3. Results pEGFP-C3 containing tBad gene was constructed successfully. Conclusion pEGFP-C3 containing tBad gene was constructed successfully and can be used to explore the function of inducing apoptosis of BCC cells.
Keywords:human Bad gene  clone  green fluorescent protein  eukaryotic expression vector  basal cell carcinoma  
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