论文部分内容阅读
目的:构建高效真核表达载体以提高细胞因子在真核细胞中的表达效率。方法:利用基因克隆技术构建了两个新的白细胞介素6(IL6)真核表达载体pAdCIIL6和p335CIL6。将它们瞬时转染COS7细胞后,利用IL6依赖株7TD1对上清中的IL6进行检测。结果:两种新建载体分别能提高IL6在真核细胞中的表达效率5.5和3.4倍。结论:腺病毒的病毒相关Ⅰ和ⅡRNA(virusasociatedⅠandⅡRNA,VAⅠandVAⅡ)和腺伴随病毒(adenoasociatedvirus,AAV)的倒转末端重复序列(invertedterminalrepeat,ITR)能提高细胞因子在真核细胞中的表达
Objective: To construct efficient eukaryotic expression vector to improve the expression of cytokines in eukaryotic cells. Methods: Two new interleukin6 (IL6) eukaryotic expression plasmids pAdCIIL6 and p335CIL6 were constructed by gene cloning technique. After they were transiently transfected COS 7 cells, the use of IL 6 dependent strains 7TD1 supernatant IL 6 were detected. Results: The two new vectors could improve the expression efficiency of IL6 in eukaryotic cells by 5.5 and 3.4 times, respectively. CONCLUSION: The inverted terminal resequence (ITR) of adenovirus-associated viral vaso-associated I and II (VAⅠandVAⅡ) and adeno-associated virus (AAV) can increase the expression of cytokines in eukaryotic cells