Sample preparation for two-dimensional gel electrophoresis

The choice of sample preparation protocol is a critical influential factor for isoelectric focusing which in turn affects the two‐dimensional gel result in terms of quality and protein species distribution. The optimal protocol varies depending on the nature of the sample for analysis and the proper...

Full description

Saved in:
Bibliographic Details
Published in:Proteomics (Weinheim) Vol. 3; no. 8; pp. 1408 - 1417
Main Authors: Shaw, Margaret M., Riederer, Beat M.
Format: Journal Article
Language:English
Published: Weinheim WILEY-VCH Verlag 01-08-2003
WILEY‐VCH Verlag
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The choice of sample preparation protocol is a critical influential factor for isoelectric focusing which in turn affects the two‐dimensional gel result in terms of quality and protein species distribution. The optimal protocol varies depending on the nature of the sample for analysis and the properties of the constituent protein species (hydrophobicity, tendency to form aggregates, copy number) intended for resolution. This review explains the standard sample buffer constituents and illustrates a series of protocols for processing diverse samples for two‐dimensional gel electrophoresis, including hydrophobic membrane proteins. Current methods for concentrating lower abundance proteins, by removal of high abundance proteins, are also outlined. Finally, since protein staining is becoming increasingly incorporated into the sample preparation procedure, we describe the principles and applications of current (and future) pre‐electrophoretic labelling methods.
Bibliography:ark:/67375/WNG-1S3V1X1C-6
ArticleID:PMIC200300471
istex:44D78D8F7F0F55FF54610232F134B8597CA34A86
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
ISSN:1615-9853
1615-9861
DOI:10.1002/pmic.200300471