User:Dhea Patel/Notebook/Hemoglobin Project/2013/02/13: Difference between revisions
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== | ==Objective== | ||
* | * Run UV-vis and Fluorescence on p-sorbitol in phosphate buffer and mannitol in tris buffer samples in either MeOH, acetone, acetonitrile, ethyl acetate, water, or chloroform. | ||
==Description== | |||
*Each solvent was used as a blank. | |||
*The data was corrected for the blank and a corrected baseline. | |||
*UV-vis scanned from 200-800nm | |||
*Fluorescence was run with an emission scan of 310-550nm at an excitation of 290nm and scan speed of 100nm/min. | |||
Revision as of 07:21, 13 February 2013
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