Team:BYU Provo/Notebook/SmallPhage/Fallexp/Period3/Dailylog
From 2013.igem.org
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* Worked on putting together Jamboree presentation and poster. | * Worked on putting together Jamboree presentation and poster. | ||
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+ | * Tried to take EM to verify mutant size - did not work very well: phage titer is too low | ||
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LP | LP | ||
- | * Performed | + | * Performed spot tests to estimate the mutant phage titer in [[Team:BYU_Provo/Notebook/SmallPhage/Fallexp/10.8 Characterization of Mutant Phage|10.8 Characterization of Mutant Phage]]. |
* Started approximately 20 mL of E coli B liquid culture overnight. | * Started approximately 20 mL of E coli B liquid culture overnight. | ||
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+ | JL | ||
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+ | * Designed primers for cloning the major and minor capsid proteins into the iGEM registry: BI309 (Xbal) and BI310 (SpeI) | ||
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* Plated the mutant phage at -7 to verify their phenotypic stability. For specifics, please see [[Team:BYU_Provo/Notebook/SmallPhage/Fallexp/10.8 Characterization of Mutant Phage|10.8 Characterization of Mutant Phage]]. | * Plated the mutant phage at -7 to verify their phenotypic stability. For specifics, please see [[Team:BYU_Provo/Notebook/SmallPhage/Fallexp/10.8 Characterization of Mutant Phage|10.8 Characterization of Mutant Phage]]. | ||
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+ | * Designed primers for more accurate sequencing: BI319 (160bp upstream from start codon) and BI320 (-160 downstream from minor capsid protein stop codon) | ||
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- | <font size="4"> ''' | + | <font size="4"> '''10/14/13''' </font> |
JL, LP | JL, LP | ||
- | * | + | * Plated more phage to look for mutants as part of [[Team:BYU_Provo/Notebook/SmallPhage/Fallexp/10.8 Characterization of Mutant Phage|10.8 Characterization of Mutant Phage]]. |
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Latest revision as of 23:54, 20 October 2013
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10/1/13 - 10/3/13 JL, LP
10/4/13 - 10/6/13 JL, LP
10/7/13 JL
10/8/13 JL
10/9/13 JL, LP
10/10/13 LP
JL
10/11/13 JL, LP
10/12/13 JL
10/13/13 JL
10/14/13 JL, LP
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