Construction of eukaryotic expression vector for EGFR gene C-terminal domain
Xiao‐Guang Chen
Abstract
Xiao‐Guang Chen
Abstract
To construct the eukaryotic expression vector containing EGFR gene C-terminal domain.EGFR gene C-terminal domain from DH 5α is cloned by PCR,and subclons it into pcDNA 3.1(+) vector.The recombinant vector is vested by double-enzyme digestion and sequencing.The target fragment(1158 bp) is obtained as expected.pcDNA3.1(+)-hEGFR eukaryotic expression vector was successfully constructed.sequence analysis of the inserted target fragment revealed the same sequence as that published in Gen Bank.The pcDNA3.1(+)-hEGFR eukaryotic expression vector was successfully constructed.
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To construct the eukaryotic expression vector containing EGFR gene C-terminal domain.EGFR gene C-terminal domain from DH 5α is cloned by PCR,and subclons it into pcDNA 3.1(+) vector.The recombinant vector is vested by double-enzyme digestion and sequencing.The target fragment(1158 bp) is obtained as expected.pcDNA3.1(+)-hEGFR eukaryotic expression vector was successfully constructed.sequence analysis of the inserted target fragment revealed the same sequence as that published in Gen Bank.The pcDNA3.1(+)-hEGFR eukaryotic expression vector was successfully constructed.
Key concepts: Vector (molecular biology), Gene, Recombinant DNA, Expression vector, Molecular biology, Biology, Computational biology, Sequence (biology)