Cloning Polymerase Chain Reaction (PCR) Products: Making T Vectors
Author(s) -
Michael R. Green,
Joseph Sambrook
Publication year - 2021
Publication title -
cold spring harbor protocols
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.674
H-Index - 51
eISSN - 1940-3402
pISSN - 1559-6095
DOI - 10.1101/pdb.prot101295
Subject(s) - polymerase chain reaction , polymerase , residue (chemistry) , chemistry , cloning (programming) , dna , microbiology and biotechnology , computational biology , stereochemistry , biology , biochemistry , gene , computer science , programming language
During polymerase chain reaction (PCR), DNA polymerases such as Taq add a single, unpaired residue—preferentially an adenosyl residue—to each 3′ end of a double-stranded amplified product. The unpaired terminal (A) residues can pair with a linear T vector that carries an unpaired 3′-thymidyl residue at each end. T vectors can be prepared in the laboratory or they may be purchased ready-made from commercial suppliers. This protocol outlines two methods in common use to generate T vectors.
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