Literature DB >> 6194142

Evaluation of five basic fluorochromes of potential use in microfluorometric studies of nucleic acids.

S K Curtis, R R Cowden.   

Abstract

Five basic fluorochromes were evaluated to determine whether or not any could be used in microfluorometric studies for the selective demonstration of nucleic acids. Only two of the fluorochromes - Nuclear Yellow (Hoechst 769121) and the phenoxyindole compound D261/37 - were found to be selective for nucleic acids, while the other three fluorochromes produced small to moderate amounts of fluorescence in preparations extracted sequentially with RNase and DNase. All of the fluorochromes could be considered "structural probes" since they produced less fluorescence in the highly condensed chromatin of thymocyte nuclei than they did in the less condensed chromatin of hepatocyte nuclei. When exposed to continuous excitation for 2-min intervals, hepatocyte nuclei stained with Nuclear Yellow or D261/37 gradually lost, respectively, approximately 21% or nearly 60% of their original fluorescence. Nuclei stained with the other three fluorochromes displayed much more rapid fading and lost more than 80% of their original fluorescence.

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Year:  1983        PMID: 6194142     DOI: 10.1007/bf00496202

Source DB:  PubMed          Journal:  Histochemistry        ISSN: 0301-5564


  17 in total

1.  Isolation of nuclei using hexylene glycol.

Authors:  W Wray; P M Conn; V P Wray
Journal:  Methods Cell Biol       Date:  1977       Impact factor: 1.441

2.  Centrifugal cytology. I. A quantitative technique for the preparation of glutaraldehyde-fixed cells for the light and scanning electron microscope.

Authors:  R C Leif; H N Easter; R L Warters; R A Thomas; L A Dunlap; M F Austin
Journal:  J Histochem Cytochem       Date:  1971-04       Impact factor: 2.479

3.  Inhibition of fading in fluorescence microscopy of fixed cells.

Authors:  D Gill
Journal:  Experientia       Date:  1979-03-15

4.  A simple method of reducing the fading of immunofluorescence during microscopy.

Authors:  G D Johnson; G M Nogueira Araujo
Journal:  J Immunol Methods       Date:  1981       Impact factor: 2.303

5.  Quantitation of fluorescence fading phenomena for identifying intracellular biopolymers.

Authors:  S S West; J F Golden; J M Menter; L D Love
Journal:  J Histochem Cytochem       Date:  1976-01       Impact factor: 2.479

6.  Fluorescence microscopy: reduced photobleaching of rhodamine and fluorescein protein conjugates by n-propyl gallate.

Authors:  H Giloh; J W Sedat
Journal:  Science       Date:  1982-09-24       Impact factor: 47.728

7.  Microfluorometric investigations of chromatin structure. I. Evaluation of nine DNA-specific fluorochromes as probes of chromatin organization.

Authors:  R R Cowden; S K Curtis
Journal:  Histochemistry       Date:  1981

8.  Four fluorochromes for the demonstration and microfluorometric estimation of RNA.

Authors:  S K Curtis; R R Cowden
Journal:  Histochemistry       Date:  1981

9.  Double retrograde neuronal labeling through divergent axon collaterals, using two fluorescent tracers with the same excitation wavelength which label different features of the cell.

Authors:  H G Kuypers; M Bentivoglio; C E Catsman-Berrevoets; A T Bharos
Journal:  Exp Brain Res       Date:  1980       Impact factor: 1.972

10.  DIPI and DAPI: fluorescence banding with only negliglible fading.

Authors:  W Schnedl; A V Mikelsaar; M Breitenbach; O Dann
Journal:  Hum Genet       Date:  1977-04-15       Impact factor: 4.132

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