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hey_howudoin2003

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  1. So, I already have a promoter cloned in a vector and I intend to study expression patterns by doing promoter bashing where I digest the DNA with blunt ended enzymes and removing the small piece and re ligating the remaining fragment.
  2. Will it be of good efficiency????
  3. Is it possible to ligate a vector cut by 2 different blunt ended restriction enzymes?
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