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目的构建大鼠RDS/peripherin真核表达载体pALTERRDS,并观察它在COS1细胞中的表达。方法将全长度的RDS/peripherincDNA(1.5kb)插入到真核表达载体pALTERMAX中,构建了RDS真核表达载体pALTERRDS。采用电穿孔技术将其转染COS1细胞,转染48h后,采用RTPCR检测RDS/peripherincDNA的表达。结果采用RTPCR方法可检测到RDS/peripherincDNA转录的mRNA。结论所构建的RDS真核表达载体可在COS1细胞中表达。
Objective To construct the rat RDS / peripherin eukaryotic expression vector pALTER RDS, and observe its expression in COS 1 cells. Methods The full-length RDS / peripherincDNA (1.5kb) was inserted into the eukaryotic expression vector pALTERMAX to construct the RDS eukaryotic expression vector pALTERRDS. The cells were transfected with COS1 cells by electroporation, and 48 hours after transfection, the expression of RDS / peripherincDNA was detected by RTPCR. Results RT-PCR method can detect RDS / peripherincDNA mRNA transcripts. Conclusion The constructed RDS eukaryotic expression vector can be expressed in COS 1 cells.