Team:Mississippi State/10 July 2008

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  1. Run 1% agarose gel w/ 3x10ul of each sample from PCR
  2. cut bands, right sample= #1(RP), left sample = #2(BKM)
  3. Purify gel using QIAgen Kit
  4. Prepare and run 1% agarose gel w/ 2ul each sample pure LiP
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