Objective: To amplify human era (Hera) gene, then express it in E.coli. Methods: Human era gene, after amplified by PCR and identified by sequencing, was inserted into the expression vector pGEX-4T3 in which exogenous...Objective: To amplify human era (Hera) gene, then express it in E.coli. Methods: Human era gene, after amplified by PCR and identified by sequencing, was inserted into the expression vector pGEX-4T3 in which exogenous gene was controlled by Ptac promoter. The recombinant plasmid pGEX-Hera was transformed into DH5 (and induced with IPTG chemically. Results: The human era gene was amplified and the sequence was correct. When the bacteria with pGEX-Hera was induced, an anticipated 65 000 protein band appeared on SDS-PAGE gel and amounted to 23% of total bacterial protein. Conclusion: The human era gene has been successfully amplified and efficiently expressed in E.coli.展开更多
To construct the bait vector with different domains of human Era in yeast two-hybrid system, then assay whether its expression product can affect the growth of yeast cells and activate the reporter genes, the cDNA fra...To construct the bait vector with different domains of human Era in yeast two-hybrid system, then assay whether its expression product can affect the growth of yeast cells and activate the reporter genes, the cDNA fragments encoding different domains of human Era was amplified by PCR, and subsequently they were cloned into pUC19. After being verified by sequencing, they were subcloned into the bait vector pGBKT7 of yeast two-hybrid system. Furthermore, these recombinant plasmids were transferred into AH109, and their expression products were assayed whether they could activate the reporter genes. The cDNA fragments encoding different domains of human Era were amplified successfully. The different domains of human Era were not toxic to AH109 and could not activate the reporter genes. Yeast two-hybrid GAL4 system could be used to fish human Era interacting protein.展开更多
基金research grant from the National NaturalScience Foundation of China (No. 39870380, 39670006) the ScienceFoundation of PLA (
文摘Objective: To amplify human era (Hera) gene, then express it in E.coli. Methods: Human era gene, after amplified by PCR and identified by sequencing, was inserted into the expression vector pGEX-4T3 in which exogenous gene was controlled by Ptac promoter. The recombinant plasmid pGEX-Hera was transformed into DH5 (and induced with IPTG chemically. Results: The human era gene was amplified and the sequence was correct. When the bacteria with pGEX-Hera was induced, an anticipated 65 000 protein band appeared on SDS-PAGE gel and amounted to 23% of total bacterial protein. Conclusion: The human era gene has been successfully amplified and efficiently expressed in E.coli.
文摘To construct the bait vector with different domains of human Era in yeast two-hybrid system, then assay whether its expression product can affect the growth of yeast cells and activate the reporter genes, the cDNA fragments encoding different domains of human Era was amplified by PCR, and subsequently they were cloned into pUC19. After being verified by sequencing, they were subcloned into the bait vector pGBKT7 of yeast two-hybrid system. Furthermore, these recombinant plasmids were transferred into AH109, and their expression products were assayed whether they could activate the reporter genes. The cDNA fragments encoding different domains of human Era were amplified successfully. The different domains of human Era were not toxic to AH109 and could not activate the reporter genes. Yeast two-hybrid GAL4 system could be used to fish human Era interacting protein.
