User:Catherine Koenigsknecht/Notebook/Experimental Biological Chemistry/2013/02/06: Difference between revisions
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*Phosphate buffer was used as a blank and was used to create the baseline. | *Phosphate buffer was used as a blank and was used to create the baseline. | ||
*Kinetics was run at 265nm using 2.38mL phosphate buffer, 600μL of 500μM stock adenosine, and 20μL ADA (as outlined in the table below). | |||
**The velocity was determined by clicking Operations > Activity Table > dAbs. The average of the dAbs values is the average slope (velocity). | |||
*5mM adenosine stock solution was too concentrated and exceeded the capacity of the UV-Vis therefore it was diluted: | *5mM adenosine stock solution was too concentrated and exceeded the capacity of the UV-Vis therefore it was diluted: |
Revision as of 09:58, 6 February 2013
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