User:Megan L. Channell/Notebook/Horseradish/2013/09/04: Difference between revisions
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|style="background-color: #EEE"|[[Image: | |style="background-color: #EEE"|[[Image:BDLlogo_notext_lr.png|128px]]<span style="font-size:22px;"> Biomaterials Design Lab</span> | ||
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<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### --> | <!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->==Adenosine and Inosine UV-Vis and Analysis== | ||
== | |||
==Objective== | |||
*Collect the data on the UV-Vis from the ionisine dilutions | |||
The inosine samples came from [[User:Megan_L._Channell/Notebook/Horseradish/2013/09/03 | yesterday's]] protocol | |||
*Calculate calibration curves for Adenosine and Inosine | |||
*Run a data regressions on the class' data | |||
==Protocol== | |||
Yesterday, our adenosine dilutions were much lower than the class' average, so we redid the adenosine samples. A new stock solutions was made using [[User:Megan_L._Channell/Notebook/Horseradish/2013/09/03 | yesterday's]] protocol and the stock solutions was made from .0809g of adenosine. | |||
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Revision as of 14:18, 8 September 2013
 Biomaterials Design Lab
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Adenosine and Inosine UV-Vis and AnalysisObjective
The inosine samples came from yesterday's protocol
ProtocolYesterday, our adenosine dilutions were much lower than the class' average, so we redid the adenosine samples. A new stock solutions was made using yesterday's protocol and the stock solutions was made from .0809g of adenosine. | |
