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Abstract
This technique is used to visualize sites of active transcription in a permeabilized cell and does not require radiolabeled molecules (e.g., [3H] Uridine). Nonradioactive ribonucleic acid (RNA) precursors (e.g., 5-bromouridine-5′-triphosphate [BrUTP]) are used and can be detected by using fluorescently labeled antibodies. Procedures for BrUTP of labeling transcription sites require manipulations that are best applied to adherent cells but can be applied, with difficulty, to cell cultures in suspension. The protocol described below is for adherent cells grown on cover slips.
Affiliation(s): (3) Department of Cell Biology, University of Massachusetts Medical School, Worcester, MA
Series: Methods in Molecular Biology  |  Volume: 285  |  Pub. Date: Jul-19-2004  |  Page Range: 29-31  |  DOI: 10.1385/1-59259-822-6:029
Subject:  Cell Biology
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