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Team:BYU Provo/Notebook/SmallPhage/Summerexp/Period1/Explist
From 2013.igem.org
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| - | | colspan="3" | <font color="#333399" size="5" font face="Calibri"> '''Small Phage | + | | colspan="3" | <font color="#333399" size="5" font face="Calibri"> |
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| + | : '''Small Phage July - August Notebook: July 1 - July 15 Experiment Listing'''</font> | ||
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| + | : <u> '''Small Phage''' </u> </font> | ||
: [[Team:BYU Provo/Notebook/SmallPhage/Winterexp|March-April]] | : [[Team:BYU Provo/Notebook/SmallPhage/Winterexp|March-April]] | ||
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<font size="4"> '''7.8 Mutagen Concentration Test - Fourth Protocol''' </font> | <font size="4"> '''7.8 Mutagen Concentration Test - Fourth Protocol''' </font> | ||
| - | + | This is our fourth round of mutagenesis. In contrast to the previous two, in which we either incubated phage with mutagen for 30 minutes or 22 hours, we tried 3 hours this time. Results from this experiment were confusing: titer between different mutagen concentration was not significantly different, although in terms of average 200ug mutagen formed the most number of plaques. After discussion, we were able to identify several source of error, one of which is the death of our stock phage. We will propagate and titer our phage next. | |
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| + | Detailed procedure: [[Team:BYU Provo/Notebook/SmallPhage/Springexp/Period3/Exp/7.8 Mutagen Concentration Test - Forth Protocol|7.8 Mutagen Concentration Test - Fourth Protocol]] | ||
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| + | <font size="4"> '''7.13 Phage Propagation Experiment''' </font> | ||
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| + | We performed two rounds of propagation to increase the titer of our phage stock. An accurate titer with x1 agar was then performed to confirm the concentration our newly generated phage stock. | ||
| - | Detailed procedure: [[Team:BYU Provo/Notebook/SmallPhage/ | + | Detailed procedure: [[Team:BYU Provo/Notebook/SmallPhage/Summer/Period1/Exp/7.13 Phage Propagation|7.13 Phage Propagation Experiment]] |
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Latest revision as of 15:34, 9 September 2013
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7.8 Mutagen Concentration Test - Fourth Protocol This is our fourth round of mutagenesis. In contrast to the previous two, in which we either incubated phage with mutagen for 30 minutes or 22 hours, we tried 3 hours this time. Results from this experiment were confusing: titer between different mutagen concentration was not significantly different, although in terms of average 200ug mutagen formed the most number of plaques. After discussion, we were able to identify several source of error, one of which is the death of our stock phage. We will propagate and titer our phage next. Detailed procedure: 7.8 Mutagen Concentration Test - Fourth Protocol
7.13 Phage Propagation Experiment We performed two rounds of propagation to increase the titer of our phage stock. An accurate titer with x1 agar was then performed to confirm the concentration our newly generated phage stock. Detailed procedure: 7.13 Phage Propagation Experiment
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