Difference between revisions of "User:Dhea Patel/Notebook/CHEM 572: ADA&Inhibitor Kinetics/2013/02/13"

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==Objective==
 
*to finish Trail 2 and run Trial 3 of ADA kinetics
 
  
==Description==
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*to baseline UV-vis, have one cuvette of phosphate buffer in reference cell and one cuvette of phosphate buffer in sample cell and run baseline from 200-400nm.
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**keep the cuvette containing phosphate buffer in the reference cell and put the adenosine + buffer + ADA in the sample cell.
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*The following table was used to create the mixtures in the cuvette.
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**[[Image:Data_Table.JPG]]
 
**In order to complete trail 2, 100uM, 150uM and 200uM [adenosine] were run.
 
**All the listed concentrations were run for trial 3.
 
  
 
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Latest revision as of 18:59, 23 September 2017

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