User:Keoni K. Gandall/Notebook/Halobacterium NCR-1 vector/2013/02/06: Difference between revisions

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|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Project name</span>
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==Entry one==
==Entry twenty six==
*Nothing here
*Today I preformed the transformations, side by side. Some things that I noticed is that the CaCl protocol (as it should be) is much simpler then the DIY TSS method, but takes more material (that luckily I have). The TSS method, I barely used anything compared to the CaCl method, even though both are bare bones.
 
*I used some of the DNA I synthesized... I used (about) 500 ng in both and REALLY hope I get something, since for 4 ug cost my more then 300$.
 
*I noticed that once I began to get amp plates out of the refrigerator, that I only had 4! So, I had to decide which to not use, the control or the "control" with pGreen. I kept the pGreen. Hopefully by tomorrow I will see nice colonies!
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Latest revision as of 22:25, 26 September 2017

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Entry twenty six

  • Today I preformed the transformations, side by side. Some things that I noticed is that the CaCl protocol (as it should be) is much simpler then the DIY TSS method, but takes more material (that luckily I have). The TSS method, I barely used anything compared to the CaCl method, even though both are bare bones.
  • I used some of the DNA I synthesized... I used (about) 500 ng in both and REALLY hope I get something, since for 4 ug cost my more then 300$.
  • I noticed that once I began to get amp plates out of the refrigerator, that I only had 4! So, I had to decide which to not use, the control or the "control" with pGreen. I kept the pGreen. Hopefully by tomorrow I will see nice colonies!