Hernan R, Heuermann K, Brizzard B
Sigma Chemical Company, St. Louis, MO 63103, USA.
Biotechniques. 2000 Apr;28(4):789-93. doi: 10.2144/00284pf01.
Three FLAG epitopes have been incorporated into the mammalian expression vector pCMV-5 to create a transient expression vector, p3XFLAG-CMV-7. The vector was designed to express FLAG fusion proteins that can be detected at tenfold lower expression levels than the current FLAG fusion protein expression system. The usefulness of this expression and detection system was demonstrated by expression of bacterial alkaline phosphatase in COS-7 cells. In addition, 3XFLAG bacterial alkaline phosphatase was expressed in Escherichia coli, purified on anti-FLAG M2 affinity gel, and detection of 500 pg of purified protein by Western blot analysis is demonstrated.
已将三个FLAG表位整合到哺乳动物表达载体pCMV-5中,以构建一个瞬时表达载体p3XFLAG-CMV-7。该载体设计用于表达FLAG融合蛋白,其可在比当前FLAG融合蛋白表达系统低十倍的表达水平下被检测到。通过在COS-7细胞中表达细菌碱性磷酸酶,证明了该表达和检测系统的实用性。此外,3XFLAG细菌碱性磷酸酶在大肠杆菌中表达,在抗FLAG M2亲和凝胶上纯化,并通过蛋白质印迹分析证明可检测到500 pg的纯化蛋白。