Electron microscopes differ from light microscopes in that they produce an image of a specimen by using a beam of electrons rather than a beam of light. Electrons have much a shorter wavelength than visible light, and this allows electron microscopes to produce higher-resolution images than standard light microscopes.
For light microscopy, the nucleus is usually stained with orcein, Giemsa, or DAPI. These “nuclear stains” do not actually stain the nucleus but rather the chromatin or DNA contents within it. Consequently, when the nuclear shape is different from the chromatin shape such as within the mitotic nucleus and many stages of conjugation, staining can give a misleading interpretation of nuclear size, position, and behavior.
By electron microscopy the nuclear envelope may be clearly visible, but the shape and position of the dynamic, sometimes elongate, Micronuclei can be difficult to observe, however each component of the micronucleus can be distintly viewed and this is where the two methods can be compared.
You measured the diameter of the micronucleus using fluorescence microscopy and electron microscopy. How do the...
In certain electron microscopy methods, the specimen is not directly imaged. How do these methods provide information about cellular structures, and what type of structures do they visualize?
1) What can you use fluorescence lifetime (FLIM) measurements for and what is the advantage compare with fluorescence intensity measurements? I have difficult to understand why FLIM is a better technique than fluorescence intensity? by better I mean the advantage FLIM have comparing to fluorescence intensity method? They say its better because FLIM is indenpendent of change in fluorescence intensity, and fluorophore concentration. But in FLIM measurement we measure the intensity of flourophore versus time? just like the fluorescence intensity...
You want to resolve structures that electron microscopy has indicated are 55 nm apart in the XY dimension. Which type of light microscopy technique(s) should you use?
Using a fluorescence microscope, you observed how the localization of GFP-Ras changes in response to the inhibitor. (8 pts total) a. GFP is a reporter protein, what does this mean? b. You used stains to visualize the nucleus and golgi bodies and the fluorescence microscope to determine whether the GFP-Ras protein was present in the golgi or nucleus. How do these stains work? i. Hoechst 34580 ii. BODIPY TR Ceramide
The great advantage of using EDS inside SEM is that we can do both Microscopy and Spectroscopy. However, there is no point in attempting to analyze regions much less than 1um in diameter with EDS in SEM. Why?
If you examined the axonemes of patients with immotile cilia syndrome by electron microscopy, would you expect to see a defect? Why or why not?
1. Fill out the following table by indicating which general technique (light microscopy (LM) or electron microscopy (EM]) could be used to observe each structure or phenomenon. Put "no" in the box if the technique could not be used. If light microscopy can be used, name one technique (bright-field, phase-contrast, fluorescence, etc.) that you think would be effective. You will find some useful information in Appendix 1 of this manual and Chapter 18 of your textbook. Structure or phenomenon Could...
1) Diameter of a coin is measured as 0.223 cm and its height (thickness) is measured as 0.024 cm and weight 5.3 grams. Calculate density of the coin and compare it with the density of copper 8.96 gr/cm3 . Could your coin be pure copper? What is the precision for each measurements 2) In a free fall experiment, when you plot height in meters versus time squared as second squared, you obtain your slope as 4.8. What is the unit...
1. Fill out the following table by indicating which general technique (light microscopy (LM) or electron microscopy [EM]) could be used to observe each structure or phenomenon. Put "no" in the box if the technique could not be used. If light microscopy can be used, name one technique (bright-field, phase-contrast, fluorescence, etc.) that you think would be effective. You will find some useful information in Appendix 1 of this manual and Chapter 18 of your textbook. Structure or phenomenon Could...
Can you tell me something about local and global alignment in detail. And about electron microscopy for structure determination of protein, and about free electron lasers also. Pleasee, thank you in advance. I really appreciate it!!!!