The pET-47b(+) plasmid features the ability to express fusion proteins with an N-terminal His?Tag? coding sequence that is cleavable with the human rhinovirus (HRV) 3C protease. The plasmid contains a strong T7lac promoter, an optimized RBS, the coding sequence for the HRV 3C protease cleavage site (LeuGluValLeuPheGlnGlyPro), and a multiple cloning site that contains restriction enzyme sites found in many other Novagen expression vectors to facilitate insert transfer. An optional C-terminal S?Tag? coding sequence is compatible with purification, detection, and quantification.
基因搜项目发展历程最早可追溯至2010年01月05日域名注册,项目发起即为促进基因资源共享,避免在基因研究工作中“重复造轮子”,节约广大科研精英的宝贵时间和精力。
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