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Article in English | WPRIM (Western Pacific) | ID: wpr-654675

ABSTRACT

T-vectors are widely used for cloning the polymerase chain reaction (PCR) products. However, the low conversion efficiency of a plasmid into the linear T-vector usually results in non-recombinants. Here, we designed a new plasmid pNBQ-T to easily select the recombinant colonies harboring PCR products. pNBQ-T plasmid, which contains a DsRed indicator gene between two Nt.BspQI restriction cassettes, each of which contains palindromic sequences susceptible to Nt.BspQI nickase (5′-GCTCTTCT


Subject(s)
Clone Cells , Cloning, Organism , Deoxyribonuclease I , Methods , Myostatin , Plasmids , Polymerase Chain Reaction
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