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作 者:尹宗生[1] 张辉[1] 张胜权[2] 王伟[1] 华兴一[1] 胡勇[1] 李光武[3]
机构地区:[1]安徽医科大学第一附属医院骨科,安徽合肥230032 [2]安徽医科大学分子生物学教研室,安徽合肥230032 [3]安徽医科大学神经生物研究所,安徽合肥230032
出 处:《第四军医大学学报》2006年第24期2212-2215,共4页Journal of the Fourth Military Medical University
基 金:国家自然科学基金(30571881);安徽省自然科学基金(050430713)
摘 要:目的:表达具备生物活性的重组小鼠Wnt-3a信号蛋白.方法:应用脂质体转染试剂将重组真核表达载体pSecTag2/HygroB-Wnt3a转染并筛选稳定表达的NIH3T3细胞,WesternBlot鉴定重组Wnt-3a蛋白的表达,并对Wnt3a/NIH3T3细胞的融合密度及抗凋亡能力给予检测.结果:Wnt-3a信号蛋白在Wnt3a/NIH3T3细胞中获得稳定表达,Wnt-3a信号蛋白能够明显提高NIH3T3细胞的融合密度及抗凋亡能力.结论:在NIH3T3细胞中表达的重组Wnt-3a信号蛋白具备生物活性.AIM: To express recombinant mouse Wnt-3a signal protein with biological activity. METHODS: The recombinant eukaryotic expression plasmid, pSecTag2/Hygro B-Wnt3a, was transfected into NIH3T3 cells by liposome, then the expressed protein was detected by Western Blot. The saturation density and the capability of suppressing apoptosis in Wnt3a/NIH3T3 cells were evaluated. RESULTS: The Wnt-3a signal protein was stably expressed in Wnt3a/NIH3T3 cells. The saturation density and the capability of suppressing apoptosis in Wnt3a/NIH3T3 cells were markedly increased. CONCLOUSION: We successfully construct the recombinant Wnt-3a signal protein with biological activity.
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