User:Mary Mendoza/Notebook/CHEM572 Exp. Biological Chemistry II/2013/03/20: Difference between revisions

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==Histogram==
* It was decided to create a histogram for each inhibitor which includes the flavonoids and the non-nucleoside, acetylsalicylic acid analogs. Each inhibitor consisted of three trials.
* From Sigma, 500 μM Kaempferol (C<sub>15</sub>H<sub>10</sub>O<sub>6</sub>, MW 286.24 g/mol) stock solution was prepared in dimethylsulfoxide (DMSO).
* A kinetic assay run of 40 μM adenosine without inhibitors was executed through the kinetics of the UVProbe system.
* After the three trials of 40 μM adenosine, aspirin trials were conducted.
* The aspirin trials did not show inhibition. A possible conclusion for the inconsistency was that the aspirin stock solution has deteriorated.
* Kaempferol trials were started.
* After examining some of the data, it was concluded to adjust the 40 μM adenosine concentration to 25 μM.


==Tables==
* The data below was taken from [[User:Dhea Patel/Notebook/CHEM 572: ADA&Inhibitor Kinetics/2013/03/20|Dhea Patel]].
*To measure the mass of Kaempferol and the volume of DMSO:
[[Image:Screen_Shot_2013-03-20_at_1.45.50_PM.png]]


*Table of volumes and concentrations:
 
[[Image:Kinetics_Histogram_table.tiff|px550]]
 




Revision as of 15:25, 8 May 2013

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