Team:Rice University/Notebook/13 July 2008

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*#Innoculated 100mL of LB with 1.0mL of O/N cultures and grew at 37*C (for all strains excluding the VCS257 containing the temperature sensitive phage.  All 5.0mL of this O/N were used to innoculate the 100mL of LB.  The Resulting culture was grown at 30*C).
*#Innoculated 100mL of LB with 1.0mL of O/N cultures and grew at 37*C (for all strains excluding the VCS257 containing the temperature sensitive phage.  All 5.0mL of this O/N were used to innoculate the 100mL of LB.  The Resulting culture was grown at 30*C).
*#All strains were grown to OD600nm of approximately 0.8 (Note: the 7524 strain never reached an appropriate optical density, however, I continued the prep with the slightly reduced titer).
*#All strains were grown to OD600nm of approximately 0.8 (Note: the 7524 strain never reached an appropriate optical density, however, I continued the prep with the slightly reduced titer).
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*#Cells were made electrocompetent following the procedure outlined [a;lsdkjf|here].
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*#Cells were made electrocompetent following the procedure outlined [[Team:Rice University/Electroporation|here]].
*#Procedure resulted in 10x40uL stocks of each of the 5 strains.
*#Procedure resulted in 10x40uL stocks of each of the 5 strains.

Latest revision as of 19:23, 16 July 2008

Sunday, July 13th

  • Taylor Stevenson
    1. Innoculated 100mL of LB with 1.0mL of O/N cultures and grew at 37*C (for all strains excluding the VCS257 containing the temperature sensitive phage. All 5.0mL of this O/N were used to innoculate the 100mL of LB. The Resulting culture was grown at 30*C).
    2. All strains were grown to OD600nm of approximately 0.8 (Note: the 7524 strain never reached an appropriate optical density, however, I continued the prep with the slightly reduced titer).
    3. Cells were made electrocompetent following the procedure outlined here.
    4. Procedure resulted in 10x40uL stocks of each of the 5 strains.






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