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Chinese Journal of Biotechnology ; (12): 956-965, 2016.
Article in Chinese | WPRIM | ID: wpr-242284

ABSTRACT

For more economical and efficient DNA clonging, pFL-XS-T, a Biobrick-T vector was constructed based on pMD18-T vector, carrying clonging regions of XbaⅠ-XcmⅠ-XcmⅠ-SpeⅠ. The results revealed that PCR products could be conveniently inserted into pFL-XS-T vevtor digested by XcmⅠby means of TA cloning. The positive frequency of recombination can meet the experimental requirements and all the plasmids obtained meet Biobrick standard. Moreover, the pFL-XS-T is compatible with other Biobrick parts, and serves as a vector for functional DNA fragments screening.


Subject(s)
Cloning, Molecular , DNA , Genetic Vectors , Plasmids , Polymerase Chain Reaction , Synthetic Biology
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