Team:BYU Provo/Notebook/SmallPhage/Summerexp/Period4/Dailylog

From 2013.igem.org

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<font size="4"> '''8/17/13''' </font>
<font size="4"> '''8/17/13''' </font>
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- Started characterizing post-CsCl phage in [[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/8.14_Mutagen_Concentration_Test_-_Seventh_Protocol|8.14 Mutagen Concentration Test - Seventh Protocol]].
+
* Started characterizing post-CsCl phage in [[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/8.14_Mutagen_Concentration_Test_-_Seventh_Protocol|8.14 Mutagen Concentration Test - Seventh Protocol]].
-
- Started approximately 10mL of E coli B liquid culture overnight.
+
* Started approximately 10mL of E coli B liquid culture overnight.
-
- Streaked out E coli B.
+
* Streaked out E coli B.
<br>
<br>
Line 44: Line 44:
<font size="4"> '''8/18/13''' </font>
<font size="4"> '''8/18/13''' </font>
-
- Continued characterization 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]].
+
* Continued characterization 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]].
-
- Started approximately 20mL of E coli B liquid culture overnight.
+
* Started approximately 20mL of E coli B liquid culture overnight.
<br>
<br>
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<font size="4"> '''8/19/13''' </font>
<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]].
+
* 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.
+
* 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.
+
* Started approximately 30 mL of E coli B liquid culture overnight.
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<font size="4"> '''8/20/13''' </font>
<font size="4"> '''8/20/13''' </font>
-
- Selected for 12 small plaques (relatively large phage) and 12 big plaques (relatively small phage) at the end of each spectrum for [[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/8.14_Mutagen_Concentration_Test_-_Seventh_Protocol|8.14 Mutagen Concentration Test - Seventh Protocol]]. Spectrum ends were chose because the likelihood of contamination between different layers of CsCl during the extraction process.
+
* Selected for 12 small plaques (S1-S12, relatively large phage) and 12 big plaques (B1-B12, relatively small phage) at respective end of spectrum for [[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/8.14_Mutagen_Concentration_Test_-_Seventh_Protocol|8.14 Mutagen Concentration Test - Seventh Protocol]]. Spectrum ends were chose because the likelihood of contamination between different layers of CsCl during the extraction process.
-
- Performed dilution series and spot test for T1, T2 (from stock), and T7.
+
* Performed dilution series and spot test for T1, T2 (from stock), and T7.
-
- Started T7 propagation.
+
* Started approximately 30 mL of E coli B liquid culture overnight.
-
 
+
-
- Started approximately 30 mL of E coli B liquid culture overnight.
+
<br>
<br>
-
<font size="4"> '''8/5/13''' </font>
+
<font size="4"> '''8/21/13''' </font>
-
- Performed Phage viability/infection test for [[Team:BYU Provo/Notebook/SmallPhage/Summerexp/8.2 Modeling phage plaque size|8.2 Modeling Phage Plaque Sizes - Preliminary Experiments]].
+
* Spot test for T7 only showed plaques up to -5. Might not be high enough for mutagenesis. Need to propagate.
-
+
-
- Discussed ideas for modeling phage plaque sizes
+
   
   
 +
* Plated the S1-S12 and B1-B12 samples.
 +
 +
* Started approximately 6 mL of E coli B liquid culture overnight
 +
<br>
<br>
-
<font size="4"> '''8/6/13''' </font>
+
<font size="4"> '''8/22/13''' </font>
 +
 
 +
* Nothing showed on the S1-S12 and B1-B12 plates. Wildtype had too many plaques (T7 at -4).
-
- Check up on the phage viability/infection test for [[Team:BYU Provo/Notebook/SmallPhage/Summerexp/8.2 Modeling phage plaque size|8.2 Modeling Phage Plaque Sizes - Preliminary Experiments]].
+
* T7 propagation.  
-
- Started 5mL of E coli B liquid culture overnight.
+
* Started approximately 20 mL of E coli liquid culture overnight.
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<br>

Revision as of 21:52, 22 August 2013


Small Phage July - August Notebook: August 17 - August 31 Daily Log



Overview
March-April
May-June
July-August
September-October

8/17/13

  • Started approximately 10mL of E coli B liquid culture overnight.
  • Streaked out E coli B.


8/18/13

  • Started approximately 20mL of E coli B liquid culture overnight.


8/19/13

  • Started approximately 30 mL of E coli B liquid culture overnight.



8/20/13

  • Selected for 12 small plaques (S1-S12, relatively large phage) and 12 big plaques (B1-B12, relatively small phage) at respective end of spectrum for 8.14 Mutagen Concentration Test - Seventh Protocol. Spectrum ends were chose because the likelihood of contamination between different layers of CsCl during the extraction process.
  • Performed dilution series and spot test for T1, T2 (from stock), and T7.
  • Started approximately 30 mL of E coli B liquid culture overnight.


8/21/13

  • 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.
  • Started approximately 6 mL of E coli B liquid culture overnight


8/22/13

  • Nothing showed on the S1-S12 and B1-B12 plates. Wildtype had too many plaques (T7 at -4).
  • T7 propagation.
  • Started approximately 20 mL of E coli 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.