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PMID: 67075 Published · ppublish English Journal Article

DIPI and DAPI: fluorescence banding with only negliglible fading.

Human genetics ·Vol. 36 ·No. 2 ·1977-04-15 ·Pages 167-72

Schnedl W, Mikelsaar AV, Breitenbach M, Dann O

Abstract

DIPI and DAPI produce distinct fluorescent bands in human chromosomes similar to quinacrine banding patterns. Additionally, the AT rich secondary constrictions in the chromosomes Nos. 1, 9 and 16 are brightly fluorescent. On the other hand the brilliantly fluorescent regions after staining with quinacrine mustard in the chromosomes Nos. 3 and 4, satellites and some other regions in the acrocentric chromosomes are less striking. The distal part of the Y, however, is clearly discernible. Thus DIPI and DAPI seem to be strictly AT specific fluorochromes like Hoechst 33258. In interphase nuclei the Y chromosome can be identified. However, quinacrines are superior for Y-body analysis in buccal, hair cell and sperm smears. BrdU labeled chromatids show reduced fluorescence intensity. The difference, however, is less apparent than after staining with Hoechst 33 258. DAPI and especially DIPI are highly resistant to UV-irradiation; there is almost no fading within 30 min when using DIPI. Moreover, fluorescence intensity is stronger than in quinicrines. When photographing, exposure times may be reduced to about one quarter compared to quinacrine mustard.

MeSH Terms
Amidines Chromosomes/analysis Fluorescent Dyes Humans Imidazoles Indoles Staining and Labeling Ultraviolet Rays
Chemicals
Amidines Fluorescent Dyes Imidazoles Indoles DAPI
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Schnedl W
Mikelsaar A V
Breitenbach M
Dann O
References (20)
20 references, click to expand
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Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
1977-04-15
Pages
167-72
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
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