| Literature DB >> 21969615 |
Abstract
Many nuclear proteins have been successfully localized using immunofluorescence microscopy. These proteins span all nuclear domains, including the nuclear envelope, nuclear lamina, nucleolus, chromatin-associated proteins, and proteins associated with RNA metabolism and nuclear bodies. This article describes a general method for localizing nuclear proteins. Cells grown on coverslips are fixed in either formaldehyde or methanol and permeabilized in Triton X-100. Incubating the cells with primary antibody and fluorescently conjugated secondary antibody allows visualization of the target antigen.Entities:
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Year: 2011 PMID: 21969615 DOI: 10.1101/pdb.prot065755
Source DB: PubMed Journal: Cold Spring Harb Protoc ISSN: 1559-6095