Team:BYU Provo/Notebook/Phage Purification/Springexp/Period5/Dailylog
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(Created page with "{{TeamBYUProvo}} <br> {| width="100%" | colspan="3" | <font color="#333399" size="5" font face="Calibri"> '''Phage Purification May - June Notebook: June 24 - June 30 Daily Log...") |
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: [[Team:BYU_Provo/Notebook/Phage_Purification/Winterexp/Period1/Exp/6.12PEGPurification|6.12 PEG Purification]] | : [[Team:BYU_Provo/Notebook/Phage_Purification/Winterexp/Period1/Exp/6.12PEGPurification|6.12 PEG Purification]] | ||
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+ | - The large phage group switched to using E. coli B instead of W3110. We will now be using E. coli B instead of W3110. Streaked plates of BL21 and B for future use. Left in the 37<sup>◦</sup> C over the weekend. | ||
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Revision as of 20:27, 1 July 2013
Phage Purification May - June Notebook: June 24 - June 30 Daily Log
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6/10/13 - Prepared RNase A for future use. - Prepared T4 and T7 cultures.
6/26/13 - Performed a titer on purified phage to test the concentration.
6/28/13 - The large phage group switched to using E. coli B instead of W3110. We will now be using E. coli B instead of W3110. Streaked plates of BL21 and B for future use. Left in the 37◦ C over the weekend.
6/17/13 - Set up CsCl gradient 6.17 CsCl Gradient - Prepared T4 and T7 cultures.
6/19/13 - Began first step of purification process using phage from 6.17 Phage Preparation. - Ran spot tests on collected band from 6.17 CsCl Gradient.
6/20/13 - Finished 6.19 PEG Purification by centrifuging solution at 10,000 g 15 minutes at 4◦ C, removing supernatant, and suspending the pellet in phage suspension buffer.
6/21/13 We centrifuged the pellet at 10,000 g for 15 min at 4◦ C after suspending it to clean up the walls of the tube.
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