User:Mary Mendoza/Notebook/CHEM 571 Experimental Biological Chemistry I/2012/10/23: Difference between revisions
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==ADA preparation== | ==ADA preparation== | ||
* All ADA procedures for this lab period was conducted by [[User:Puja Mody/Notebook/Chem 571: Gold Nanoparticles/2012/10/23|Puja Mody]]. The same approach was conducted during [[User:Mary Mendoza/Notebook/CHEM 571 Experimental Biological Chemistry I/2012/09/19|09/19/2012]] | * All ADA procedures for this lab period was conducted by [[User:Puja Mody/Notebook/Chem 571: Gold Nanoparticles/2012/10/23|Puja Mody]]. The same approach was conducted during [[User:Mary Mendoza/Notebook/CHEM 571 Experimental Biological Chemistry I/2012/09/19|09/19/2012]] | ||
* This was a two day procedure continued by Michael Nagle on the following day, [[User:Michael F. Nagle/Notebook/Chem 571/2012/10/23|10/23/2012]] | |||
* The main concept for the procedure: ''E. coli'' was transformed to express ADA. After a 4 h. protein expression on an incubator shaker, the solution were centrifuge. The supernatant was collected and stored since this contained the soluble ADA while the pellets (cellular debris) were discarded. | * The main concept for the procedure: ''E. coli'' was transformed to express ADA. After a 4 h. protein expression on an incubator shaker, the solution were centrifuge. The supernatant was collected and stored since this contained the soluble ADA while the pellets (cellular debris) were discarded. | ||
Revision as of 07:49, 7 December 2012
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ADA preparation
Au/lysozyme solutions
AAS of Au/BSA solution of 10/17/12
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