feulgen densitometry
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Genome ◽  
2000 ◽  
Vol 43 (3) ◽  
pp. 449-451 ◽  
Author(s):  
Eva M Temsch ◽  
Johann Greilhuber

Genome size variation within species is a frequently reported, but still a controversial problem. In the present study, we re-evaluated recently published Feulgen densitometric data on genome size and its infraspecific variation in Arachis hypogaea, and also conducted measurements in one accession of its wild relative A. monticola. The methods applied were propidium iodide flow cytometry and Feulgen densitometry using Pisum sativum as an internal standard. The 2C DNA contents previously published cannot be confirmed, but values obtained in this study are about half as large. Additionally, we could not reproduce the previously reported 1.15-fold variation within A. hypogaea; our data indicate genome size stability between respective accessions of this species. Based on 8.84 pg (2C) for Pisum sativum the DNA amounts (2C) were: 5.914 pg in A. hypogaea, and 5.979 pg in A. monticola.Key words: Arachis, genome size, flow cytometry, Feulgen densitometry.


Plant Biology ◽  
1999 ◽  
Vol 1 (5) ◽  
pp. 538-540 ◽  
Author(s):  
J. Greilhuber ◽  
Monika Baranyi ◽  
J. Greilhuber
Keyword(s):  

1992 ◽  
Vol 63 (2) ◽  
pp. 153
Author(s):  
M. Kirsch-Volders ◽  
P. Segers ◽  
S. Haesen ◽  
Ph. Castelain ◽  
Hummelen^P. Van

1991 ◽  
Vol 73 (2-3) ◽  
pp. 44a-44a
Author(s):  
Pascale SEGERS ◽  
Sonja HAESEN ◽  
Phillipe CASTELAIN ◽  
Paul HUMMELEN ◽  
Micheline KIRSCH-VOLDERS

1983 ◽  
Vol 31 (10) ◽  
pp. 1224-1232 ◽  
Author(s):  
R J Sklarew

A method has been developed for densitometric estimation of the Feulgen-stained DNA content of 3H-labeled nuclei in autoradiographs in conjunction with automated grain counting using a Quantimet Imaging System. Refinements in the methodology are reported which include 1) the incorporation of an Image-Editor Module into the Quantimet module configuration; 2) the optimization of incident illumination based upon evaluation of various light sources; 3) changes in the optical configuration which reduce glare and minimize the level of monitor shading correction; 4) the optimization of scanner sensitivity; and 5) the evaluation of cell-flattening and staining with respect to densitometry resolution and sensitivity. These refinements resulted in a CV of less than 6.4% in the G-1 and G-2 DNA peaks of rat kidney cells in autoradiographs compared to the previous CV of 10.5%, and a G-2 to G-1 ratio of 2.025. For a fixed field position the CV was 5.1% and the replication error less than 1.0%.


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