With recent advances in molecular biology, it is now possible to construct genomic sequences and then evaluate the protein produced by those sequences. Ever-increasing portions of the genome are being investigated for their functions or for the effect sequence changes might have on them. Such study may entail testing the function of an unknown region of the genome, or mutating a sequence in a particular region to see how protein function or binding to other molecules might be affected. In these cases, using a complete plasmid for transfection is tedious, requiring time-consuming cloning, amplification, and purification of a plasmid construct. If multiple variants are to be tested, it would be much simpler if the PCR product could be tested directly, and a plasmid construct made only once the sequence of interest is identified. more