Comparison of areas of quinacrine mustard fluorescence and modified Giemsa staining in human metaphase chromosomes |
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Authors: | P Aula E Saksela |
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Affiliation: | Laboratory of Cytogenetics, III Department of Pathology, and Children''s Hospital, University of Helsinki, Helsinki, Finland |
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Abstract: | The methods of quinacrine mustard fluorescence and modified Giemsa staining were compared in view of the structural details revealed in human mitotic chromosomes derived from the peripheral blood of normal healthy humans. Over the chromatids both techniques produced a crossbanding pattern where larger segments of heavy staining in the latter technique and the fluorescing bands in the former occurred at similar locations. The centromeric heterochromatin, intensely stained with Giemsa was, however, negative in fluorescence, except for chromosome no. 3 and less often no. 6. The regularly occurring secondary constrictions in chromosomes 1, 9, and 16 behaved generally like areas of centromeric heterochromatin. The area of secondary constriction in the Y chromosome as also that of chromosome 9 in the ASG modification of the Giemsa technique was both non-fluorescent and non-staining. |
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