Analysis of centromere size in human chromosomes 1, 9, 15, and 16 by electron microscopy

Genome ◽  
1991 ◽  
Vol 34 (5) ◽  
pp. 710-713 ◽  
Author(s):  
Laura Sanchez ◽  
Paulino Martínez ◽  
Vicente Goyanes

Human chromosomes were treated with 5-azacytidine and analyzed by whole-mount electron microscopy. This base analogue produces undercondensation of heterochromatin and separation of the centromere from the bulk of pericentromeric heterochromatin in chromosomes 1, 9, 15, and 16, which allows clear delimitation of the centromere regions. A quantitative analysis of centromeres showed that chromosomes 1, 9, and 16 have centromeres of different size. The centromere of chromosome 15 is similar in size to that of chromosome 9 and different from those of chromosomes 1 and 16. No interindividual variation for centromere size was found. A positive correlation between centromere and chromosome size was found for the chromosomes analyzed.Key words: centromere size, human chromosomes, electron microscopy.

1974 ◽  
Vol 49 (3) ◽  
pp. 133-136
Author(s):  
C. Wolff ◽  
C. Gilly ◽  
C. Mouriquand

Author(s):  
J. H. Hayden

In a previous study, Allen video-enhanced constrast/differential interference constrast (AVEC-DIC) microscopy was used in conjunction with immunofluorescence microscopy to demonstrate that organelles and vesicle move in either direction along linear elements composed of microtubules. However, this study was limited in that the number of microtubules making up a linear element could not be determined. To overcome this limitation, we have used AVEC-DIC microscopy in conjunction with whole mount electron microscopy.Keratocytes from Rana pipiens were grown on glass coverslips as described elsewhere. Gold London Finder grids were Formvar- and carbon coated, and sterilized by exposure to ultraviolet light. It is important to select a Formvar film that gives a grey reflection when it is floated on water. A silver film is too thick and will detract from the image in the light microscope.


Author(s):  
Conly L. Rieder

The behavior of many cellular components, and their dynamic interactions, can be characterized in the living cell with considerable spatial and temporal resolution by video-enhanced light microscopy (video-LM). Indeed, under the appropriate conditions video-LM can be used to determine the real-time behavior of organelles ≤ 25-nm in diameter (e.g., individual microtubules—see). However, when pushed to its limit the structures and components observed within the cell by video-LM cannot be resolved nor necessarily even identified, only detected. Positive identification and a quantitative analysis often requires the corresponding electron microcopy (EM).


1980 ◽  
Vol 54 (2) ◽  
pp. 163-169 ◽  
Author(s):  
O. A. Podugolnikova ◽  
A. P. Korostelev

BioTechniques ◽  
2014 ◽  
Vol 57 (6) ◽  
Author(s):  
Mohammed Yusuf ◽  
Bo Chen ◽  
Teruo Hashimoto ◽  
Ana Katrina Estandarte ◽  
George Thompson ◽  
...  

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