Team:BYU Provo/Notebook/SmallPhage/Summerexp/Period4/Dailylog
From 2013.igem.org
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* Spot test for T7 only showed plaques up to -5. Might not be high enough for mutagenesis. Need to propagate. | * Spot test for T7 only showed plaques up to -5. Might not be high enough for mutagenesis. Need to propagate. | ||
- | * Plated the S1-S12 and B1-B12 samples. | + | * Plated the S1-S12 and B1-B12 samples in [[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/8.14_Mutagen_Concentration_Test_-_Seventh_Protocol|8.14 Mutagen Concentration Test - Seventh Protocol]]. |
* Started approximately 6 mL of E coli B liquid culture overnight | * Started approximately 6 mL of E coli B liquid culture overnight | ||
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* Nothing showed on the S1-S12 and B1-B12 plates. Wildtype had too many plaques (T7 at -4). | * Nothing showed on the S1-S12 and B1-B12 plates. Wildtype had too many plaques (T7 at -4). | ||
- | * T7 propagation. | + | * T7 propagation for [[Team:BYU Provo/Notebook/SmallPhage/Summerexp/8.26 Mutagen Concentration Test|8.26 Mutagen Concentration Test - Eighth Protocol]]. |
* Started approximately 20 mL of E coli liquid culture overnight. | * Started approximately 20 mL of E coli liquid culture overnight. | ||
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- | <font size="4"> '''8/ | + | <font size="4"> '''8/23/13''' </font> |
- | - | + | - Repeated plating of S1-S12 and B1-B12 in [[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/8.14_Mutagen_Concentration_Test_-_Seventh_Protocol|8.14 Mutagen Concentration Test - Seventh Protocol]]. |
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- | <font size="4"> '''8/ | + | <font size="4"> '''8/24/13''' </font> |
- | - | + | - Still no bacteria or phage plaques showed up for S1-S12 and B1-B12 in [[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/8.14_Mutagen_Concentration_Test_-_Seventh_Protocol|8.14 Mutagen Concentration Test - Seventh Protocol]] -> We decided to focus on [[Team:BYU Provo/Notebook/SmallPhage/Summerexp/8.26 Mutagen Concentration Test|8.26 Mutagen Concentration Test - Eighth Protocol]] instead |
- | + | - Purified T7 phage propagation and performed a spot test to estimate the titer of this fresh stock (8.24). | |
- | + | ||
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- | - | + | - Started approximately 10mL of E coli B liquid culture overnight |
<br> | <br> | ||
- | <font size="4"> '''8/ | + | <font size="4"> '''8/25/13''' </font> |
- | - Started approximately | + | - Titer was performed for T7 phage 8.24 stock at -6 and -7 to gain a more accurate estimate of phage concentration. |
+ | |||
+ | - Started approximately 10mL of E coli B liquid culture overnight. | ||
<br> | <br> | ||
- | <font size="4"> '''8/ | + | <font size="4"> '''8/26/13''' </font> |
- | - Performed | + | - Performed the actual mutagenesis procedure in [[Team:BYU Provo/Notebook/SmallPhage/Summerexp/8.26 Mutagen Concentration Test|8.26 Mutagen Concentration Test - Eighth Protocol]]. |
- | - | + | - Phage Purification Team was able to run the CsCl gradient right after the completion of mutagenesis. |
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- | + | ||
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- | + | ||
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- Started approximately 20mL of E coli B liquid culture overnight. | - Started approximately 20mL of E coli B liquid culture overnight. | ||
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- | <font size="4"> '''8/ | + | <font size="4"> '''8/27/13''' </font> |
- | - | + | - Spot test was performed for the post CsCl aliquots (for both control and mutated group) to estimate phage concentration in each. For specific procedure please refer to [[Team:BYU Provo/Notebook/SmallPhage/Summerexp/8.26 Mutagen Concentration Test|8.26 Mutagen Concentration Test - Eighth Protocol]]. |
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<br> | <br> | ||
- | <font size="4"> '''8/ | + | <font size="4"> '''8/30/13''' </font> |
- | + | - Started approximately 20mL of E coli B liquid culture overnight. | |
- | + | ||
- | - Started approximately | + | |
<br> | <br> | ||
- | <font size="4"> '''8/ | + | <font size="4"> '''8/31/13''' </font> |
- | - | + | - Further dilution series and spot test was performed to gain a more accurate idea of phage distribution in CsCl gradient. Specific procedures can be found at [[Team:BYU Provo/Notebook/SmallPhage/Summerexp/8.26 Mutagen Concentration Test|8.26 Mutagen Concentration Test - Eighth Protocol]]. |
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<br> | <br> | ||
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{{TeamBYUProvoFooter}} | {{TeamBYUProvoFooter}} |
Revision as of 21:32, 1 September 2013
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8/17/13
8/18/13
8/19/13
8/20/13
8/21/13
8/22/13
8/23/13 - Repeated plating of S1-S12 and B1-B12 in 8.14 Mutagen Concentration Test - Seventh Protocol.
8/24/13 - Still no bacteria or phage plaques showed up for S1-S12 and B1-B12 in 8.14 Mutagen Concentration Test - Seventh Protocol -> We decided to focus on 8.26 Mutagen Concentration Test - Eighth Protocol instead - Purified T7 phage propagation and performed a spot test to estimate the titer of this fresh stock (8.24). - Started approximately 10mL of E coli B liquid culture overnight
8/25/13 - Titer was performed for T7 phage 8.24 stock at -6 and -7 to gain a more accurate estimate of phage concentration. - Started approximately 10mL of E coli B liquid culture overnight.
8/26/13 - Performed the actual mutagenesis procedure in 8.26 Mutagen Concentration Test - Eighth Protocol. - Phage Purification Team was able to run the CsCl gradient right after the completion of mutagenesis. - Started approximately 20mL of E coli B liquid culture overnight.
8/27/13 - Spot test was performed for the post CsCl aliquots (for both control and mutated group) to estimate phage concentration in each. For specific procedure please refer to 8.26 Mutagen Concentration Test - Eighth Protocol.
8/30/13 - Started approximately 20mL of E coli B liquid culture overnight.
8/31/13 - Further dilution series and spot test was performed to gain a more accurate idea of phage distribution in CsCl gradient. Specific procedures can be found at 8.26 Mutagen Concentration Test - Eighth Protocol.
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