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A new method for PCR products cloning - T-A clone technique

Xin Bo Li, Xiao Song Zhao, De Tian, Yi Zhu, Tai Yao

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Abstract

A new method for PCR products cloning T A cloning technique is introduced. pBluescript SK(+) plasmid was extracted by modified alkali lysis method. A blunt ends was generated using restriction enzyme Eco RⅤ, then T A cloning vector was prepared in the presence of Taq DNA polymerase and dTTP. β actin cDNA fragment was cloned into the above T A cloning vector. After the recombinant plasmids were digested by Eco RⅠ and Hin dⅢ, an expected size of β actin cDNA fragment was obtained .

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What this paper is about

A new method for PCR products cloning T A cloning technique is introduced. pBluescript SK(+) plasmid was extracted by modified alkali lysis method. A blunt ends was generated using restriction enzyme Eco RⅤ, then T A cloning vector was prepared in the presence of Taq DNA polymerase and dTTP. β actin cDNA fragment was cloned into the above T A cloning vector. After the recombinant plasmids were digested by Eco RⅠ and Hin dⅢ, an expected size of β actin cDNA fragment was obtained .

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Available abstract

A new method for PCR products cloning T A cloning technique is introduced. pBluescript SK(+) plasmid was extracted by modified alkali lysis method. A blunt ends was generated using restriction enzyme Eco RⅤ, then T A cloning vector was prepared in the presence of Taq DNA polymerase and dTTP. β actin cDNA fragment was cloned into the above T A cloning vector. After the recombinant plasmids were digested by Eco RⅠ and Hin dⅢ, an expected size of β actin cDNA fragment was obtained .

Key concepts: Cloning (programming), Molecular biology, Cloning vector, Recombinant DNA, Plasmid, Complementary DNA, Molecular cloning, Restriction enzyme

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