User:Catherine Koenigsknecht/Notebook/Experimental Biological Chemistry/2013/02/06
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==Description== | ==Description== | ||
| - | *5mM adenosine stock solution was | + | #UVProbe was opened. |
| + | ##Window > 1. Kinetics | ||
| + | ##Methods Icon | ||
| + | ###Wavelength: 265nm | ||
| + | ###Duration: 300 seconds (5minutes) | ||
| + | ###OK | ||
| + | #Shimadzu CPS-Controller was set to 25°C. | ||
| + | ##wait for the temperature to raise to 25°C | ||
| + | #place the sample in the cell and click start. | ||
| + | |||
| + | *Phosphate buffer was used as a blank and was used to create the baseline. | ||
| + | |||
| + | *5mM adenosine stock solution was too concentrated and exceeded the capacity of the UV-Vis therefore it was diluted: | ||
**This table is the volumes of 5mM adenosine and phosphate buffer used to make the new adenosine stock solutions. | **This table is the volumes of 5mM adenosine and phosphate buffer used to make the new adenosine stock solutions. | ||
***[[Image:Screen_Shot_2013-02-05_at_9.01.20_PM.png]] | ***[[Image:Screen_Shot_2013-02-05_at_9.01.20_PM.png]] | ||
Revision as of 12:53, 6 February 2013
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