Cite as: Cold Spring Harb. Protoc.; 2006; doi:10.1101/pdb.prot4571

This Protocol
Right arrow Full Text
Right arrow Update/discuss this protocolDiscussion icon
Right arrow Alert me when this protocol is cited
Right arrow Alert me when comments are published
Right arrow Alert me if a correction is posted
Services
Right arrow Similar protocols in this database
Right arrow Alert me to new releases of protocols
Right arrow Save to Personal Folders
Right arrow Download to citation manager
Right arrow Printer-friendly versionPrinter-friendly version
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ji, H.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Ji, H.
Related Collections
Right arrow Cell Biology, general
Right arrow Subcellular Fractionation
Right arrow Molecular Biology, general
Right arrow Proteins and Proteomics, general
Right arrow Chromatography, general
Right arrow Multi-Dimensional Chromatography
Right arrow Electrophoresis, general
Right arrow Electrophoresis of Proteins
Right arrowRelated Protocols
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
Legend icon

protocolProtocol

Preparation of Eukaryotic Lysates for 2D Gel Electrophoresis

Hong Ji

This protocol was adapted from "Preparative 2D Gel Electrophoresis with Immobilized pH Gradients," Chapter 4 in Proteins and Proteomics (ed. Simpson). Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, USA, 2003.


INTRODUCTION

Cultured mammalian cell lines are widely used as study models in biomedical research. The protocol described here has been used successfully for many human colon carcinoma cell lines and fibroblast cell lines. Although most cellular proteins can be extracted by this protocol, some DNA-binding proteins may not be recovered. If DNA-binding proteins are to be studied, a nuclease (e.g., Benzonase) should be included. Expression proteomic studies frequently require the detection of low-abundance proteins.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

Related Protocols

Radioisotopic Labeling of Eukaryotic Cell Proteins Using 35S
Hong Ji
CSH Protocols 2006: 4572. [Abstract] [Full Text]

Radioisotopic Labeling of Eukaryotic Cell Proteins Using 32P
Hong Ji
CSH Protocols 2006: 4573. [Abstract] [Full Text]

Preparative 2D Gel Electrophoresis with Immobilized pH Gradients: Rehydration of IPG Strips for Isoelectric Focusing of Proteins
Wayne R. Stochaj, Tom Berkelman, and Nancy Laird
CSH Protocols 2006: 4574. [Abstract] [Full Text]