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Rapid (Ligase-Free) Subcloning of Polymerase Chain Reaction Products

  • Alan R. Shuldiner
  • Keith Tanner
Protocol
  • 107 Downloads
Part of the Springer Protocols Handbooks book series (SPH)

Abstract

The polymerase chain reaction (PCR) is a versatile, widely used method for the production of a very large number of copies of a specific DNA molecule (1,2). For some applications, it is advantageous to subclone the PCR product into a plasmid vector for subsequent replication in bacteria (3, 4, 5, 6). Subcloning the PCR product into a plasmid vector has several advantages: The amplified fragment can be sequenced with greater reliability, only one allele is sequenced per clone, and the vector containing the PCR product may be used for other molecular biological experiments, e.g., in vitro transcription, transfection, and further amplification in bacteria.

Keywords

Polymerase Chain Reaction Polymerase Chain Reaction Product Plasmid Vector Addition Sequence Polymerase Chain Reaction Fragment 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Humana Press Inc., Totowa, NJ 2000

Authors and Affiliations

  • Alan R. Shuldiner
    • 1
  • Keith Tanner
    • 1
  1. 1.Johns Hopkins University School of MedicineBaltimore

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