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It is particularly relevant to use the FISH method following chronic or past exposure, since FISH offers the possibility to detect and use stable translocations for accurate biological dosimetry.
Monitoring of BCL2 translocations was done with the Fluorescence-In-Situ-Hybridization (FISH) method.
To report a simple and efficient fluorescence in situ hybridization (FISH) method for preimplantation genetic diagnosis (PGD).
Compared to conventional methods of bacterial identification, the FISH method produced positive results for > 90% of the samples tested.
The FISH method used in this study was suitable for the detection of simazine-degrading bacteria and could be a useful indicator of the potential of soil bioremediation.
In this study the fluorescence in situ hybridization (FISH) method was used to detect Pedomicrobium in iron and manganese incrusted biofilms.
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This PNA-FISH method was then systematically optimized, employing response surface methodology (RS M.
Using a flow cytometry-based (Flow-FISH) method of measuring telomere length in individual cells, we have studied the effects of aging and sublethal irradiation on hematopoietic cells of longlived C57BL/6 and short-lived DBA/2 mouse strains.
To further confirm the results obtained using the TRF assay, we analyzed telomere length variation throughout the life of the zebrafish using the more sensitive and specific Q-FISH method.
G9a-shRNA, SUV39H1-shRNA or control-shRNA-treated PC3 cells were evaluated for telomere shortening using the Telo-FISH method to visualize telomeres in interphase cell populations, as described previously [18].
The PNA-FISH method was performed according to manufacturer's recommendations.
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