User:Trisha I. Ibeh/Notebook/Trisha Notebook/2013/09/04: Difference between revisions
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==Objective== | ==Objective== | ||
Finish up the lab from the previous day by taking the UV- Vis spectrum of inosine and doing data analysis. | |||
==Description== | ==Description== |
Revision as of 03:31, 21 September 2013
Biomaterials Design Lab | <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page <html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html> </html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html> |
ObjectiveFinish up the lab from the previous day by taking the UV- Vis spectrum of inosine and doing data analysis. DescriptionFluorescence spectroscopy is another way to analyze molecular samples. InstructionsEach group will pick a different protein (bovine serum albumin, horseradish peroxidase, pepsin, adenosine deaminase, hemoglobin). You'll need to make 4 samples ranging from 10uM to 0.5uM. Remember, we don't have a lot of most of these proteins, so figure out how to make a stock solution using as little solid protein as possible. The fluorescence cuvette needs only 200uL, so you don't need to make more than that for each concentration that you're measuring.
NotesI made a stock solution of BSA today. Here is the info: BSA solution 0.0104g BSA (MW = 66776g/mol) in 0.0100mL water → 15.6μM
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