User:Andrew W Long/Notebook/Protein Modification/2014/10/17: Difference between revisions
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== | ==Data Analysis and Kinetics Workup== | ||
* | *Import all data from run into Ocean_Optics kinetics template and save. | ||
*Copy data from every 15 minutes into sheet 3. Start time is t=-120s, followed by -60, 0, 60, etc. | |||
*Perform a "time zero" correction by subtracting the absorbance at each time by the absorbance at t=0 for each corresponding wavelength. | |||
**For example, this will look like B2-$D2. Drag the crosshatch in the lower left corner of the first cell to perform this correction on all cells. | |||
***The dollar sign makes the value subtracted correspond to the correct wavelength at t=0. | |||
*Now perform a "baseline" correction by clicking on the first empty cell, and typing =(first cell from previous data set)-average(the absorbances at the corresponding wavelengths 800nm and higher). In practice, this will look something like: U2-average(U$1748:U$2049). Drag the crosshatch in the lower left corner of the first cell to perform this correction on all cells. | |||
*Finally, copy the times, then click "paste special," and select "values" under Paste and by ckeck "transpose." This will transpose the times to the y axis. Next copy the absorbances at 420nm from the previous section, and transpose those on the y axis as well. This will show how the concentration of the protein (absorbance peak at 420nm changes over time). | |||
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Latest revision as of 00:26, 27 September 2017
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Data Analysis and Kinetics Workup
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