Team:BYU Provo/Notebook/SmallPhage/Springexp/Period4/Dailylog
From 2013.igem.org
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<font size="4"> '''6/17/13''' </font> | <font size="4"> '''6/17/13''' </font> | ||
- | - Plated 5 controls and 50 selection plates (500ug at -2) as part of selection 1 in [[Team:BYU Provo/Notebook/SmallPhage/Springexp/Period3/Exp/6.12 Mutagen Concentration Test - Perfected Protocol|6.12 Mutagen Concentration Test - | + | - Plated 5 controls and 50 selection plates (500ug at -2) as part of selection 1 in [[Team:BYU Provo/Notebook/SmallPhage/Springexp/Period3/Exp/6.12 Mutagen Concentration Test - Perfected Protocol|6.12 Mutagen Concentration Test - Second Protocol]] |
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<font size="4"> '''6/19/13''' </font> | <font size="4"> '''6/19/13''' </font> | ||
- | - We performed Large Plaque Confirmation 1 as part of [[Team:BYU Provo/Notebook/SmallPhage/Springexp/Period3/Exp/6.12 Mutagen Concentration Test - Perfected Protocol|6.12 Mutagen Concentration Test - | + | - We performed Large Plaque Confirmation 1 as part of [[Team:BYU Provo/Notebook/SmallPhage/Springexp/Period3/Exp/6.12 Mutagen Concentration Test - Perfected Protocol|6.12 Mutagen Concentration Test - Second Protocol]] |
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- Made more x8 top agar. | - Made more x8 top agar. | ||
- | - Because the large plaque confirmation 1 had contamination from overnight (the LB was contaminated the next day), we redid the confirmation procedure: Large Plaque Confirmation 2 in [[Team:BYU Provo/Notebook/SmallPhage/Springexp/Period3/Exp/6.12 Mutagen Concentration Test - Perfected Protocol|6.12 Mutagen Concentration Test - | + | - Because the large plaque confirmation 1 had contamination from overnight (the LB was contaminated the next day), we redid the confirmation procedure: Large Plaque Confirmation 2 in [[Team:BYU Provo/Notebook/SmallPhage/Springexp/Period3/Exp/6.12 Mutagen Concentration Test - Perfected Protocol|6.12 Mutagen Concentration Test - Second Protocol]]. |
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Revision as of 19:08, 27 June 2013
Small Phage May - June Notebook: June 17 - June 30 Daily Log
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6/17/13 - Plated 5 controls and 50 selection plates (500ug at -2) as part of selection 1 in 6.12 Mutagen Concentration Test - Second Protocol
6/18/13 - Started approximately 50mL of BL21 liquid culture overnight.
6/19/13 - We performed Large Plaque Confirmation 1 as part of 6.12 Mutagen Concentration Test - Second Protocol
6/23/13 - Started 40mL of BL21 liquid culture overnight.
6/24/13 - Made more x8 top agar. - Because the large plaque confirmation 1 had contamination from overnight (the LB was contaminated the next day), we redid the confirmation procedure: Large Plaque Confirmation 2 in 6.12 Mutagen Concentration Test - Second Protocol.
6/26/13 - Made about 50ml of BL21 liquid culture overnight
6/27/13 - Started the mutagenesis procedure for 6.27_Mutagen_Concentration_Test_-_Third_Protocol
6/5/13 - Discussed plans for the selection process of 5.20 Mutagen Concentration Experiment and calculated the needed volume of agar, overnight, and phage - Made 500mL x8 agar - Performed dilution series to generate enough 200ug -4 phage stock for selection.
6/6/13 - Started approximately 50mL of BL21 liquid culture overnight.
6/7/13 - Performed the selection process of 5.20 Mutagen Concentration Experiment. Specifically, we plated 45 plates of 200ug mutagen, -4 phage dilution using x8 agar. 5 plates of 0ug, -3 phage dilution were also done a control.
6/9/13 - Started 21mL of BL21 overnight.
6/10/13 - Made 1250mL of x8 top agar - Attempted to amplify phage from larger plaques in 5.20 Mutagen Concentration Experiment
6/11/13 - Started approximately 70mL of BL21 liquid culture overnight
6/12/13 - Perfected protocol for applying mutagen to phage - Started 6.12 Mutagen Concentration Test - Perfected Protocol
6/13/13 - Started approximately 30mL of BL21 liquid culture overnight.
6/14/13 - Titered the mutagenesis product from Wednesday as part of 6.12 Mutagen Concentration Test - Perfected Protocol
6/16/13 - Started approximately 100mL of BL21 liquid culture overnight.
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