Double-Label Analysis
| Abstract |
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The detection of radiolabeled proteins is of fundamental importance in experimental biology. 35S- and 14C-labeled proteins can provide investigators with information about protein expression, synthesis, and degradation. Moreover,
posttranslational modifications, such as phosphorylation, can be studied with the use of 32P. Traditional methods for detecting radiolabeled proteins involve somewhat lengthy exposures to photographic film. Quantitation
from film-based autoradiography can be achieved by densitometry of repeated and various exposures to films because of the
small linear dynamic range of photographic film.
Affiliation(s): (2) Department of Chemical Engineering, Cornell University, Ithaca, NY
(3) Department of Biology, California Institute of Technology, Pasadena, CA
(3) Department of Biology, California Institute of Technology, Pasadena, CA
Book Title: 2-D Proteome Analysis Protocols
Series: Methods in Molecular Biology | Volume: 112 | Pub. Date: Sep-24-1998 | Page Range: 291-295 | DOI: 10.1385/1-59259-584-7:291
Subject: Biochemistry
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