Team:Warsaw/Calendar-Main/30 June 2009

From 2009.igem.org

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<h3>cox sequence</h3>
<h4>Seba</h4>
<h4>Seba</h4>
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<li>Transformation of E. coli DH5alfa</li>
<li>Transformation of E. coli DH5alfa</li>
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<p>Methods:</p>
<p>Methods:</p>
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<li><p>iiiiii

Revision as of 17:40, 7 July 2009


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PCR inv

Kama


Tasks:

  • Amplification of inv

Methods:

  • PCR mixture's composition:

    2,5ul pfu buffer (Fermentas), 2,5ul MgSO4 (Fermentas), 1,5ul primers, 1ul dNTPs (10 mM)(new), 1ul template (Yersinia), 0,5ul pfu turbo polymerase (KNGiE), 1ul DMSO solution was topped up with H2O to 25ul.
  • PCR programs:
  • inv

     4min 95°C 
    (30s 95°C, 1min 54°C , 4min15s 72°C)x31
    10min 72°C
    ~ 7°C
  • Electrophoretic separation on 1% agarose gel

  • Results:

    • Gel (from left)
    1. GeneRuler DNA Ladder Mix #SM0333 (Fermentas)
    2. inv
    3. inv control -

    Notes:

    • No product


    cox sequence

    Seba


    Tasks:

    • Transformation of E. coli DH5alfa
    • Methods:

    • iiiiii {{WarNotebookEnd}}