Cite as: Cold Spring Harb. Protoc.; 2006; doi:10.1101/pdb.prot4576

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 Stochaj, W. R.
Right arrow Articles by Laird, N.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Stochaj, W. R.
Right arrow Articles by Laird, N.
Related Collections
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

Preparative 2D Gel Electrophoresis with Immobilized pH Gradients: IEF of Proteins in an IEF-Dedicated Electrophoresis Unit

Wayne R. Stochaj, Tom Berkelman, and Nancy Laird

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

This protocol describes a method for separating proteins based on their net charge using the technique of isoelectric focusing (IEF) on immobilized pH gradient (IPG) gels, providing the first dimension of the 2D separation. In this protocol, the IPG gels are focused using self-contained instruments for IEF. These high-voltage systems allow fewer manipulations of the IPG gels, resulting in less error, strip mix-up, contamination, air contact, or urea crystallization. Because rehydration and IEF can be performed consecutively within a single unit, these two steps can be performed unattended overnight. Finally, faster separations and sharper focusing are possible due to the higher voltage available in these instruments.


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

Multiple SDS-PAGE on Vertical Electrophoresis Units
Angelika Görg, Oliver Drews, and Walter Weiss
CSH Protocols 2006: 4232. [Extract] [Full Text]

SDS-PAGE of Proteins
Richard J. Simpson
CSH Protocols 2006: 4313. [Extract] [Full Text]

Preparative 2D Gel Electrophoresis with Immobilized pH Gradients: SDS-PAGE of Proteins
Wayne R. Stochaj, Tom Berkelman, and Nancy Laird
CSH Protocols 2006: 4559. [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]

Preparative 2D Gel Electrophoresis with Immobilized pH Gradients: Isoelectric Focusing of Proteins in a Multipurpose Flatbed Electrophoresis Unit
Wayne R. Stochaj, Tom Berkelman, and Nancy Laird
CSH Protocols 2006: 4575. [Abstract] [Full Text]

Preparation of Vertical SDS Slab Gels: Casting a Single Homogeneous Gel
Wayne R. Stochaj, Tom Berkelman, and Nancy Laird
CSH Protocols 2006: 4582. [Abstract] [Full Text]

Preparation of Vertical SDS Slab Gels: Simultaneous Casting of Multiple-Gradient Gels
Wayne R. Stochaj, Tom Berkelman, and Nancy Laird
CSH Protocols 2006: 4583. [Abstract] [Full Text]