## Abstract The aim of this study was to develop a procedure to remove the TOβPROβ3 fluorescent dye from tissue sections and restain with TOβPROβ3, still allowing calculation of DNA content and distribution by confocal laser scanning microscopy (CLSM). This would allow repeated measurements on the
Fading correction for fluorescence quantitation in confocal microscopy
β Scribed by Toril A. Nagelhus; Geir Slupphaug; Hans E. Krokan; Tore Lindmo
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 933 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0196-4763
No coin nor oath required. For personal study only.
β¦ Synopsis
Quantitative analysis in confocal microscopy meets with several problems such as fading of the fluorophore during scanning and attenuation of the fluorescence in thick tissue specimens. The present study reports a quantitative investigation of the enzyme uracil-DNA glycosylase (UDG), which removes uracils from DNA. For this study we developed a fading correction algorithm which takes into account both the number of prior scans in the specimen, and the differences in fading through the specimen from each prior scan, presumably due to Werences in laser intensity at various axial distances fiom the focus position. On this point, our findings are in contrast with results reported in other well known papers, and indicate different Edding at various distances from the laser focus position. The correction procedure can and should be established for the same specimen, but on a different part of the specimen from that used in the actual biological study. Calibration can thus be done on an unknown or inhomogenous object.
For a series of confocal xy-scans through the immunostained cells, a corrected summation image representing total FITC-fluorescence related to UDG was obtained. Both noise removal and fading corrections were performed on each image in the series before the summation image was made. Estimates of total amounts of UDG localized in the cells and nuclei, respectively, could then be obtained. Measurement of the total cellular UDG-content by flow cytometry was also performed in order to make a comparison of the two methods for quantitative analysis. For both methods a range of approximately 4.5 was obtained between total UDG-content of cells at the 5 and 95 percentage points.
π SIMILAR VOLUMES
## Abstract Previously, we have carried out extensive quantitative analysis of FΓΆrster (or fluorescence) resonance energy transfer (FRET) data to show that polymeric IgA receptors and their ligands cluster in endocytic membranes in the process of sorting and trafficking in polarized cells. Here, we
a b s t r a c t Due to photo-toxicity, fluorescence microscopy imaging is a trade-off between signal to noise ratio, total observation time and spatio-temporal resolution. We propose a new and simple method to quantify the signal-dependent and the non-signal-dependent components of the noise from a