Literature DB >> 69519

Ag-staining of nucleolus organizer regions of chromosomes after A-,C-, G-, or R-banding procedures.

R Tantravahi, D A Miller, O J Miller.   

Abstract

Metaphase chromosome preparations were made from leukocyte cultures of normal individuals. The cells were fixed in methanol:acetic acid (3:1 v/v), then dropped on cold, wet slides which were air-dried before storage at 4 degrees C. The slides were stained to identify the chromosomes by one of the following procedures: (1) Quinacrine. Slides were stained for 10 min in quinacrine mustard solution, rinsed in running tap water for 2 min, and mounted in Tris-maleat buffer, pH 5.6.

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Year:  1977        PMID: 69519     DOI: 10.1159/000130782

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  5 in total

1.  A rapid technique for producing silver-stained nucleolus organizer regions and trypsin-giemsa bands on human chromosomes.

Authors:  W M Howell; D A Black
Journal:  Hum Genet       Date:  1978-07-12       Impact factor: 4.132

2.  Cytogenetic examination of the NOR activity in a proband with 13/13 translocation and in her relatives.

Authors:  H Zanki; S Hahmann
Journal:  Hum Genet       Date:  1978-09-19       Impact factor: 4.132

3.  A simple combined Ag-I/RHG technique for human metaphase chromosomes.

Authors:  J E Dipierri; J Fraisse
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  Unilateral radial aplasia and trisomy 22 mosaicism.

Authors:  F Dulitzky; F Shabtal; J Zlotogora; I Halbrecht; E Elian
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

5.  A Drosophila melanogaster cell line tested for the presence of active NORs by silver staining.

Authors:  E Privitera
Journal:  Chromosoma       Date:  1980       Impact factor: 4.316

  5 in total

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