The Ag stainability of the nucleolus organizer region (NOR) was studied in the acrocentric chromosomes identified by Q banding of cultured lymphocytes in 41 karyotypically normal persons (33 males and 8 females) originating from southeast Estonia. The data obtained are compared with those establishe
Negative silver staining in A-T and satellite DNA-rich regions of human chromosomes
โ Scribed by William Mike Howell; Thomas E. Denton
- Publisher
- Springer
- Year
- 1976
- Tongue
- English
- Weight
- 662 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0009-5915
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โฆ Synopsis
Human metaphase chromosomes were stained with silver following a pretreatment with a heated alkaline solution. The most conspicuous feature of the stained metaphases was the omission of silver staining in the secondary constrictions of chromosomes 1,9 and 16, and on the distal Yq. Our evidence indicates that the negative silver binding is due to the preferential removal or alteration of non-histone proteins associated with these regions. The cytochemical significance of these findings is discussed.
๐ SIMILAR VOLUMES
A combination of the silver-staining method of the nucleolus organizer regions (NORs) with a Giemsa-banding method is described. This double staining allows a rapid identification of the NOR-bearing chromosomes.
A series of partial inversions of the heterochromatic C-band of chromosome 9 have been stained with distamycin A plus 4',6-diamidino-2-phenyl-indol-2HCl (DA/DAPI) and found to consist of three classes: (a) those in which only the C-band in the long arm fluoresces with DA/DAPI (these are the most fre
Ag-staining of the nucleolus organizer region (NOR) was studied in the acrocentric chromosomes identified by Q-banding in repeated lymphocyte and skin fibroblast cultures from three different individuals. A similar pattern of Ag-stainability of NORs was found in the two tissues in each individual. S
The secondary constriction (SC) regions of human chromosomes A1, C9, and E16 were preferentially stained with Giemsa when the mitotic cells in a hypotonic solution were heated in a water bath before fixation. The staining intensity of these regions increased from E16 through A1 to C9. The SC region