User:Megan L. Channell/Notebook/Horseradish/2013/09/04: Difference between revisions
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==Data== | ==Data== | ||
A UV-Vis spectra of the new adenosine samples and the inosine samples were collected. The parameters for the UV-Vis were measured between 450 and 200nm. The peak for the insonie spectra was at 249nm. This wavelength was used when calculating the calibration curve. | A UV-Vis spectra of the new adenosine samples and the inosine samples were collected. The parameters for the UV-Vis were measured between 450 and 200nm. The peak for the insonie spectra was at 249nm while the adenosine was 259nm. This wavelength was used when calculating the calibration curve. | ||
[[Image:Inosine 9 4 2013 cmj UVVIS.jpg]] | [[Image:Inosine 9 4 2013 cmj UVVIS.jpg]] |
Revision as of 14:48, 8 September 2013
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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. DataA UV-Vis spectra of the new adenosine samples and the inosine samples were collected. The parameters for the UV-Vis were measured between 450 and 200nm. The peak for the insonie spectra was at 249nm while the adenosine was 259nm. This wavelength was used when calculating the calibration curve. |