User:Matthew R Skorski/Notebook/471 - Exp BioChem/2015/10/28: Difference between revisions
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==Results== | ==Results== | ||
The image below shows the intensity for the fluorescence of samples and blanks from 400 to 650 nm. | The image below shows the intensity for the fluorescence of samples and blanks from 400 to 650 nm. | ||
[[]] | [[Image:2015 10 28 Fluorescence of Raw Data.png]] | ||
To find the concentrations of peptide released at the various time intervals the samples and blanks had the area of their intensity integrated from 420 nm to 650 nm. The equation (Wavelength2 - Wavelength1)/2*0.5 was used and the sums of each interval totaled. The samples were then corrected for by subtracting the total area of the blank from the total area of the sample. The resulting intensities were then used to calculate the concentrations based off the calibration curve made on [[User:Matthew_R_Skorski/Notebook/471_-_Exp_BioChem/2015/10/07|10/07/15]]. The graph below shows the concentrations of the peptides as a function of time. | To find the concentrations of peptide released at the various time intervals the samples and blanks had the area of their intensity integrated from 420 nm to 650 nm. The equation (Wavelength2 - Wavelength1)/2*0.5 was used and the sums of each interval totaled. The samples were then corrected for by subtracting the total area of the blank from the total area of the sample. The resulting intensities were then used to calculate the concentrations based off the calibration curve made on [[User:Matthew_R_Skorski/Notebook/471_-_Exp_BioChem/2015/10/07|10/07/15]]. The graph below shows the concentrations of the peptides as a function of time. | ||
[[]] | [[Image:2015 10 28 Fluorescence Concentrations.png | ||
]] | |||
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Revision as of 20:34, 24 November 2015
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ObjectiveTo analyze the activity of proteinase k at 1 μM using fluorescence DescriptionThe guide for analyzing a protease with fluorescence can be found here at Dr. Hartings notebook
ResultsThe image below shows the intensity for the fluorescence of samples and blanks from 400 to 650 nm. To find the concentrations of peptide released at the various time intervals the samples and blanks had the area of their intensity integrated from 420 nm to 650 nm. The equation (Wavelength2 - Wavelength1)/2*0.5 was used and the sums of each interval totaled. The samples were then corrected for by subtracting the total area of the blank from the total area of the sample. The resulting intensities were then used to calculate the concentrations based off the calibration curve made on 10/07/15. The graph below shows the concentrations of the peptides as a function of time. [[Image:2015 10 28 Fluorescence Concentrations.png ]] |