Abstract
RNA synthesis has traditionally been investigated by a laborious and time-consuming radiographic method involving incorporation of tritiated uridine. Now a faster non-radioactive alternative has emerged, based on immunocytochemical detection. This method utilizes the brominated RNA precursor bromouridine, which is taken into a cell, phosphorylated, and incorporated into nascent RNA. The BrU-substituted RNA is detected by permeabilizing the cells and staining with certain anti-BrdU antibodies. This dynamic approach yields information complementing that provided by cellular RNA content analysis at a given time and may be of value in studies of cellular activation and gene expression.
Original language | English |
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Journal | Current protocols in cytometry / editorial board, J. Paul Robinson, managing editor ... [et al.] |
Volume | Chapter 7 |
Pages (from-to) | Unit 7.12 |
DOIs | |
Publication status | Published - 2001 |
Keywords
- Animals
- Antigens
- Cell Membrane
- Cell Nucleus
- Cell Separation
- Flow Cytometry
- Gene Expression
- Humans
- RNA
- Time Factors
- Uridine