Team:Rice University/Notebook/5 June 2008

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(Thursday 5 June)
 
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**Prepared gel electrophoresis of digestions from the previous day with 1Kb standard
**Prepared gel electrophoresis of digestions from the previous day with 1Kb standard
[[Image:20080604_gel.jpg|100px|left]]
[[Image:20080604_gel.jpg|100px|left]]
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(from left to right, lane 1: 1Kb, lane 2: lambda with HindIII, lane 3: lambda with XhoI/HindIII)
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(from right to left)
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<BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR>
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<BR>lane 1: 1Kb standard
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<BR>lane 2: NEB lambda with HindIII
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<BR>lane 3: NEB lambda with XhoI/HindIII)
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<BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR>
*Taylor Stevenson
*Taylor Stevenson
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**XL1-Blue MR cells were prepared for phage infection as specified in the phage packaging manual [https://static.igem.org/mediawiki/2008/6/6a/Packaging_Extract.pdf] and infected with phage at roughly a 1/10 pfu/cfu ratio.  Resulting phage/bacteria mixture was incubated @ 37*C for 20 min and then streaked onto an LB plate.  Plate was incubated @ 30*C O/N. 
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**'''Result'''-approximately 100 possibly lysogenic colonies grew on plate.
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<BR><BR><BR><BR>
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{| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center"
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!align="center"|[[Team:Rice_University|Home]]
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!align="center"|[[Team:Rice_University/Team|The Team]]
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!align="center"|[[Team:Rice_University/Project|The Project]]
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!align="center"|[[Team:Rice_University/Parts|Parts Submitted to the Registry]]
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!align="center"|[[Team:Rice_University/Modeling|Modeling]]
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!align="center"|[[Team:Rice_University/Notebook|Notebook]]
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|}

Latest revision as of 20:38, 16 July 2008

Thursday 5 June

  • Selim Sheikh:
    • Prepared gel electrophoresis of digestions from the previous day with 1Kb standard
20080604 gel.jpg

(from right to left)
lane 1: 1Kb standard
lane 2: NEB lambda with HindIII
lane 3: NEB lambda with XhoI/HindIII)










  • Taylor Stevenson
    • XL1-Blue MR cells were prepared for phage infection as specified in the phage packaging manual [1] and infected with phage at roughly a 1/10 pfu/cfu ratio. Resulting phage/bacteria mixture was incubated @ 37*C for 20 min and then streaked onto an LB plate. Plate was incubated @ 30*C O/N.
    • Result-approximately 100 possibly lysogenic colonies grew on plate.





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