840:153g:Projects/project23/2012/10/25

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Cloning of the OmcF gene Main project page
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Continuation of the Mutagenesis Reaction

  • On Tuesday, we ran the gel for last week's PCR products. The high concentration of 1:20 template DNA, and a low concentration of 1:200 were prepared with water for each the upstream and downstream fragments. Our nomenclature used is three-part, and outlined below.
  • 1.)Primer configuration
    • N = no primers used
    • P = outside primers used
  • 2.)Template DNA concentration
    • + = 1:20
    • - = 1:200
  • 3.)Annealing temperature for PCR, in °C


  • Our positive control was standard template DNA and associated primers from lab stock
  • Our negative control had outside primers and no template


  • We loaded our samples as follows:
  • Top Lane:
  1. 100 bp ladder
  2. P+55
  3. P+60
  4. P+65
  5. Positive Control
  6. P-55
  7. P-60
  8. P-65
  9. 100 bp ladder


  • Bottom Lane:
  1. 100 bp ladder
  2. N+55
  3. N+60
  4. N+65
  5. Negative Control
  6. N-55
  7. N-60
  8. N-65
  9. 100 bp ladder


  • We ran these on a 1% agarose gel for 30min at 120V


  • Results:



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