Difference between revisions of "Optical Microscopy: Part 2 Report Outline"
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− | + | # Microscope documentation | |
− | + | ## Include an updated block diagram of your microscope. | |
− | + | # Images | |
− | + | ## Include figures with images of the 0.84 μm and 3.26 μm fluorescent microsphere samples, and the stained cell samples (with and without Cyto-D). | |
− | + | ##* For each sample, create 1 figure with 5 panels. | |
− | + | ##* The panels of the figure should be: A) unprocessed image; B) reference image; C) dark image; D) flat-field corrected image; and E) histogram. | |
− | + | ##* In the caption, specify the exposure and gain settings. Each image should have a scale bar. State the dimension of the scale bar in the caption. | |
− | + | ##* For panel E, plot histograms of the unprocessed, dark, reference, and corrected image on the same set of axes. Plot <tt>log10( count )</tt> on the vertical axis and intensity on the horizontal axis. Use a line plot instead of a bar chart for the histogram. | |
− | + | ## Image profile | |
− | + | ##* For one reference, dark and bead or cell sample image set, plot an intensity profile across the diagonals. Place all three profiles on a single set of axes. (Use the <tt>improfile</tt> command in MATLAB.) #Discussion | |
− | + | ## How did your beam expander design affect your images? | |
− | + | ## What differences did you observe between the cells with and without CytoD? | |
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Revision as of 22:33, 17 February 2015
- Microscope documentation
- Include an updated block diagram of your microscope.
- Images
- Include figures with images of the 0.84 μm and 3.26 μm fluorescent microsphere samples, and the stained cell samples (with and without Cyto-D).
- For each sample, create 1 figure with 5 panels.
- The panels of the figure should be: A) unprocessed image; B) reference image; C) dark image; D) flat-field corrected image; and E) histogram.
- In the caption, specify the exposure and gain settings. Each image should have a scale bar. State the dimension of the scale bar in the caption.
- For panel E, plot histograms of the unprocessed, dark, reference, and corrected image on the same set of axes. Plot log10( count ) on the vertical axis and intensity on the horizontal axis. Use a line plot instead of a bar chart for the histogram.
- Image profile
- For one reference, dark and bead or cell sample image set, plot an intensity profile across the diagonals. Place all three profiles on a single set of axes. (Use the improfile command in MATLAB.) #Discussion
- How did your beam expander design affect your images?
- What differences did you observe between the cells with and without CytoD?
- Include figures with images of the 0.84 μm and 3.26 μm fluorescent microsphere samples, and the stained cell samples (with and without Cyto-D).