Anti-Fading Agents for Confocal Immunofluorescence: Colocalization of Nuclear Polypeptides
- 1 January 1995
- journal article
- research article
- Published by Taylor & Francis in Biotechnic & Histochemistry
- Vol. 70 (1) , 40-45
- https://doi.org/10.3109/10520299509108315
Abstract
We evaluated the performance of four anti-fading agents during acquisition of multiple optical sections near the widest diameter of Drosophila accessory gland nuclei using indirect immunofluorescence and confocal laser scanning microscopy. Two commercially available agents, Vectashield and SlowFade showed anti-fading properties that alleviated fluorochrome fading associated with the acquisition of multiple fluorescent optical Z-series from a single specimen by a confocal laser scanning system. Using these reagents, we were able to colocalize polypeptides through immunostained whole Drosophila nuclei.Keywords
This publication has 12 references indexed in Scilit:
- Device to Prepare Extruded Nuclei and Chromosome SquashesBiotechnic & Histochemistry, 1994
- Localization of a myosin heavy chain-like polypeptide to Drosophila nuclear pore complexes.Proceedings of the National Academy of Sciences, 1991
- Chromosomes and chromatin structure: the extrachromosomal karyoskeletonCurrent Opinion in Cell Biology, 1989
- Relation of chromosome structure and gene expressionPhilosophical Transactions of the Royal Society of London. B, Biological Sciences, 1987
- Biosynthesis and interconversion of Drosophila nuclear lamin isoforms during normal growth and in response to heat shock.The Journal of cell biology, 1987
- A myosin heavy-chain-like polypeptide is associated with the nuclear envelope in higher eukaryotic cells.The Journal of cell biology, 1986
- Photometric analysis of antifading reagents for immunofluorescence with laser and conventional illumination sources.Journal of Histochemistry & Cytochemistry, 1985
- In situ localization of DNA topoisomerase II, a major polypeptide component of the Drosophila nuclear matrix fraction.Proceedings of the National Academy of Sciences, 1985
- Fluorescence Microscopy: Reduced Photobleaching of Rhodamine and Fluorescein Protein Conjugates by n -Propyl GallateScience, 1982
- A simple method of reducing the fading of immunofluorescence during microscopyJournal of Immunological Methods, 1981