Published in Gene Therapy Weekly, April 16th, 2009
"However, the number of epitope tags available in a convenient format is still low, and interference with protein function by the epitope, particularly if it is large, is not uncommon. To address these limitations and broaden the utility of the method, we constructed a set of convenient template plasmids designed for PCR-based C-terminal tagging with 10 different, relatively short peptide...
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Source: Gene Therapy Weekly (2009-04-16)
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