Optical Microscopy: Part 2 Report Outline

1. Microscope documentation
   1. Include an updated block diagram of your microscope.
2. Images
   1. Include a figure with an images of the 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.
   2. 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.)
3. Discussion
   1. How did your beam expander design affect your images?
   2. What differences did you observe between the cells with and without CytoD?