User:Mary Mendoza/Notebook/CHEM 571 Experimental Biological Chemistry I/2012/10/23: Difference between revisions
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|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Project name</span> | |style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Project name</span> | ||
|style="background-color: #F2F2F2" align="center"| | |style="background-color: #F2F2F2" align="center"|[[File:Report.png|frameless|link={{#sub:{{FULLPAGENAME}}|0|-11}}]][[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|[[File:Resultset_previous.png|frameless|link={{#lnpreventry:{{FULLPAGENAME}}}}]][[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]] }}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]][[File:Resultset_next.png|frameless|link={{#lnnextentry:{{FULLPAGENAME}}}}]]}} | ||
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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. | ||
==Au/lysozyme solutions== | ==Au/lysozyme solutions== | ||
* The calculations were supposed to be posted on the notebook of [[User:Michael F. Nagle/Notebook/Chem 571/2012/10/23|Michael Nagle]]. | * The calculations were supposed to be posted on the notebook of [[User:Michael F. Nagle/Notebook/Chem 571/2012/10/23|Michael Nagle]]. | ||
* The calculation the author had executed for stock solution preparation is on [[User:Mary Mendoza/Notebook/CHEM 571 Experimental Biological Chemistry I/2012/10/17|10/17/2012]]. The lysozyme stock solution was 15.24 μM and the gold was at 8.24 mM. | |||
* It was decided that the lysozyme would be kept at a 1.5 μM concentration for all sample varying the Au concentration. The same mole ratios from Au/BSA were used 60, 80, 100, 120, 128, 130, 132, 133, 134, 136, 138, 140, 160, and 170. | |||
* When the Au/lysozyme solutions were made, Nagle placed the rack in the Thermo Scientific incubator at 50°C for 4h. | * When the Au/lysozyme solutions were made, Nagle placed the rack in the Thermo Scientific incubator at 50°C for 4h. | ||
Latest revision as of 22:10, 26 September 2017
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ADA preparation
Au/lysozyme solutions
AAS of Au/BSA solution of 10/17/12
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