18/09/13

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Revision as of 13:57, 18 September 2013 by AliceHaworth (Talk | contribs)

Making and running an agarose gel

  • Making a 3% agarose gel to run Tod PCR fusion genes from 17/09
  • This is to determine that the digestion works
  • Running the gel with digested and undigested samples to observe the difference
  • Digested samples were taken from the digestions the Tod genes from previous day
  • 100ng of both samples were run against a 100kb ladder


Morninggel 180913.jpg


Rows are as follow:100bp ladder, undigested x, digested x, undigested b, digested b, undigested f, digested f

Plating out TOD operon bacteria

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