"
Team:BYU Provo/Notebook/SmallPhage/Summerexp/Period4/Dailylog
From 2013.igem.org
| Line 50: | Line 50: | ||
<br> | <br> | ||
| - | <font size="4"> '''8/ | + | <font size="4"> '''8/19/13''' </font> |
| + | |||
| + | - Plaque test of post-CsCl phage in [[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/8.14_Mutagen_Concentration_Test_-_Seventh_Protocol|8.14 Mutagen Concentration Test - Seventh Protocol]]. | ||
| + | |||
| + | - Discussed modeling result of [[Team:BYU Provo/Notebook/SmallPhage/Summerexp/8.16 Modeling phage plaque size|8.16 Modeling Phage Plaque Sizes - Experiment One]] with Dr. Grose -> need to repeat for T1 and T2 starting from dilution series and spot test. | ||
| + | |||
| + | - Started approximately 30 mL of E coli B liquid culture overnight. | ||
| - | |||
<br> | <br> | ||
Revision as of 16:15, 20 August 2013
| ||
|
|
8/17/13 - Started characterizing post-CsCl phage in 8.14 Mutagen Concentration Test - Seventh Protocol. - Started approximately 10mL of E coli B liquid culture overnight. - Streaked out E coli B.
8/18/13 - Continued characterization of post-CsCl phage in 8.14 Mutagen Concentration Test - Seventh Protocol. - Started approximately 20mL of E coli B liquid culture overnight.
8/19/13 - Plaque test of post-CsCl phage in 8.14 Mutagen Concentration Test - Seventh Protocol. - Discussed modeling result of 8.16 Modeling Phage Plaque Sizes - Experiment One with Dr. Grose -> need to repeat for T1 and T2 starting from dilution series and spot test. - Started approximately 30 mL of E coli B liquid culture overnight.
8/4/13 - Started E coli liquid culture over night
8/5/13 - Performed Phage viability/infection test for 8.2 Modeling Phage Plaque Sizes - Preliminary Experiments. - Discussed ideas for modeling phage plaque sizes
8/6/13 - Check up on the phage viability/infection test for 8.2 Modeling Phage Plaque Sizes - Preliminary Experiments. - Started 5mL of E coli B liquid culture overnight.
8/7/13 - Performed spot test to estimate phage titerfor 8.2 Modeling Phage Plaque Sizes - Preliminary Experiments. - Phage Purification Group started the purification process with CsCl gradient.
8/8/13 - Started approximately 15mL of E coli B liquid culture overnight.
8/9/13 - Performed Preliminary Titer for 8.2 Modeling Phage Plaque Sizes - Preliminary Experiments.
8/11/13 - Started approximately 20mL of E coli B liquid culture overnight.
8/12/13 - Performed titer - repeat for 8.2 Modeling Phage Plaque Sizes - Preliminary Experiments based on the results from 8.10 preliminary titer test. - Started T1 propagation. - Made accurate x2 top agar as preparation for 8.16 Modeling Phage Plaque Sizes - Experiment One.
8/13/13 - Started approximately 20mL of E coli B liquid culture overnight.
8/14/13 - Performed mutagenesis and spot test for 8.14 Mutagen Concentration Test - Seventh Protocol. - Performed spot test for T1 propagation. Spotted 5uL of -2 through -7 dilutions.
8/15/13 - T1 propagation revealed plaques on each of the tested dilutions, suggesting that this propagated T1 phage stock has a titer of at least 109 pfu/mL -> more accurate spot test / titer needed to determine the exact phage concentration. - Started approximately 30mL of E coli B liquid culture overnight.
8/16/13 - Started 8.16 Modeling Phage Plaque Sizes - Experiment One. - Phage Purification team performed the CsCl gradient for 8.14 Mutagen Concentration Test - Seventh Protocol.
| |
