2004
DOI: 10.1590/s1415-47572004000200012
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A rapid alternative technique for obtaining silver-positive patterns in chromosomes

Abstract: Silver nitrate chromosome staining to evidence nucleolar organizer regions (NORs) is a widely adopted methodology. The aim of the present work was to improve this technique, reducing the preparation time without decreasing the quality of the results. Microwave irradiation proved to be quite efficient and reliable for this purpose, as it allowed to identify Ag-NORs equivalent to those obtained by the conventional procedure and also to reduce the concentration of the employed reagents, as well as the precipitati… Show more

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Cited by 25 publications
(13 citation statements)
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References 16 publications
(17 reference statements)
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“…DAPI/CMA 3 staining was carried out as described by Schweizer (1976) with modifications by Guerra and Souza (2002). Ag-NOR staining was performed according Multiple NORs and karyotype variation in S. xanthotricha to Howell and Black (1980) with modifications by Kavalco and Pazza (2004), using 25% AgNO 3 , 1% gelatin, and 0.25% formic acid. A minimum of 10 metaphases per specimen were analyzed.…”
Section: Methodsmentioning
confidence: 99%
“…DAPI/CMA 3 staining was carried out as described by Schweizer (1976) with modifications by Guerra and Souza (2002). Ag-NOR staining was performed according Multiple NORs and karyotype variation in S. xanthotricha to Howell and Black (1980) with modifications by Kavalco and Pazza (2004), using 25% AgNO 3 , 1% gelatin, and 0.25% formic acid. A minimum of 10 metaphases per specimen were analyzed.…”
Section: Methodsmentioning
confidence: 99%
“…Fluorochrome staining (DAPI/CMA 3 ) was performed following Schweizer (1980). The nucleolar organizing regions (NORs) were identified by silver nitrate staining (Howell and Black 1980) with a few modifications (Kavalco and Pazza 2004). We analyzed 20 metaphases per individual, and the bestquality ones were photographed under an Olympus CX-41 microscope.…”
Section: Chromosome Preparation and Bandingmentioning
confidence: 99%
“…The cell suspension was centrifuged at 1000 rpm for 6 min and the cells fixed in methanol:acetic acid (3:1). Freshly prepared slides were submitted to silver nitrate (Kavalco and Pazza, 2004) and acridine orange staining (Abrams et al, 1993), and FISH (Viegas-Péquignot, 1992) using as probe a recombinant plasmid (HM123) containing a fragment of Xenopus laevis 28S rDNA, biotinlabeled by nick-translation reaction. The slides with the different staining were analyzed in a light and fluorescence microscope (Axioskop 2 -Zeiss) fitted with an image analyzer.…”
Section: Cell Suspension and Staining Proceduresmentioning
confidence: 99%