Literature DB >> 6168915

Lucifer dyes--highly fluorescent dyes for biological tracing.

W W Stewart.   

Abstract

Lucifer dyes are intensity fluorescent 4-aminonaphthalimides which are readily visible in living cells at concentrations and levels of illumination at which they are nontoxic. Because of their low molecular weight they frequently pass from one cell to another; this widespread phenomenon, termed dye-coupling, is thought to reveal functional relationships between cells. Lucifer dyes can also be used for ultrastructural tracing by comparison of electron micrographs with light micrographs of the same thin section. In addition, they show promise for backfilling neurones through cut nerves, for visualizing the results of retrograde axonal transport and for the covalent labeling of macromolecules.

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Year:  1981        PMID: 6168915     DOI: 10.1038/292017a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  65 in total

1.  Synthesis and photophysical characterizations of thermal-stable naphthalene benzimidazoles.

Authors:  Sule Erten-Ela; Serdar Ozcelik; Esin Eren
Journal:  J Fluoresc       Date:  2011-01-29       Impact factor: 2.217

Review 2.  Structural neurobiology: missing link to a mechanistic understanding of neural computation.

Authors:  Winfried Denk; Kevin L Briggman; Moritz Helmstaedter
Journal:  Nat Rev Neurosci       Date:  2012-02-22       Impact factor: 34.870

3.  Leydig neuron activity modulates heartbeat in the medicinal leech.

Authors:  E A Arbas; R L Calabrese
Journal:  J Comp Physiol A       Date:  1990-11       Impact factor: 1.836

4.  Short-term culturing of teleost crystalline lenses combined with high-resolution optical measurements.

Authors:  J Marcus Schartau; Ronald H H Kröger; Bodil Sjögreen
Journal:  Cytotechnology       Date:  2010-04-17       Impact factor: 2.058

5.  Electrical behaviour of myenteric neurones in the gastric corpus of the guinea-pig.

Authors:  M Schemann; J D Wood
Journal:  J Physiol       Date:  1989-10       Impact factor: 5.182

6.  Fusion of cultured dog kidney (MDCK) cells: I. Technique, fate of plasma membranes and of cell nuclei.

Authors:  U Kersting; H Joha; W Steigner; B Gassner; G Gstraunthaler; W Pfaller; H Oberleithner
Journal:  J Membr Biol       Date:  1989-10       Impact factor: 1.843

7.  Limitations of the scrape-loading/dye transfer technique to quantify inhibition of gap junctional intercellular communication.

Authors:  S C McKarns; D J Doolittle
Journal:  Cell Biol Toxicol       Date:  1992 Jan-Mar       Impact factor: 6.691

8.  A fast perfusion system for single cell physiology optimized for microscopes with water immersion objectives.

Authors:  F Kirchhoff; C Ohlemeyer; H Kettenmann
Journal:  Pflugers Arch       Date:  1992-04       Impact factor: 3.657

9.  gamma-Aminobutyric acid antagonists decrease junctional communication between L-horizontal cells of the retina.

Authors:  M Piccolino; J Neyton; P Witkovsky; H M Gerschenfeld
Journal:  Proc Natl Acad Sci U S A       Date:  1982-06       Impact factor: 11.205

10.  Properties of enzymatically isolated skeletal fibres from mice with muscular dystrophy.

Authors:  S I Head; D G Stephenson; D A Williams
Journal:  J Physiol       Date:  1990-03       Impact factor: 5.182

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