Review the Concepts

1. Both light and electron microscopy are commonly used to visualize cells, cell structures, and the location of specific molecules. Explain why a scientist may choose one or the other microscopy technique for use in research.

2. The magnification possible with any type of microscope is an important property, but its resolution, the ability to distinguish between two very closely apposed objects, is even more critical. Describe why the resolving power of a microscope is more important for seeing finer details than its magnification. What is the formula used to describe the resolution of a microscope lens, and what are the limitations placed on the values in the formula?

3. Why are chemical stains required for visualizing cells and tissues with the basic light microscope? What advantage do fluorescent dyes and fluorescence microscopy provide in comparison to the chemical dyes used to stain specimens for light microscopy? What advantages do confocal and deconvolution microscopy provide in comparison to conventional fluorescence microscopy?

4. In certain electron microscopy methods, the specimen is not directly imaged. How do these methods provide information about cellular structure, and what types of structures do they visualize? What limitation applies to most forms of electron microscopy?

5. What is the difference between a cell strain, a cell line, and a clone?

6. Explain why the process of cell fusion is necessary to produce monoclonal antibodies used for research.

7. Much of what we know about cell function depends on experiments using specific cells and specific parts (e.g., organelles) of cells. What techniques do scientists commonly use to isolate cells and organelles from complex mixtures, and how do these techniques work?

8. Hoechst 33258 is a chemical dye that binds specifically to DNA in live cells, and when excited by UV light, it fluoresces in the visible spectrum. Name and describe one specific method, employing Hoechst 33258, an investigator would use to isolate fibroblasts in the G2 phase of the cell cycle from those fibroblasts in interphase.

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