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...
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Published in: | Proteomics (Weinheim) Vol. 3; no. 8; pp. 1408 - 1417 |
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Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
Weinheim
WILEY-VCH Verlag
01-08-2003
WILEY‐VCH Verlag |
Subjects: | |
Online Access: | Get full text |
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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. |
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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 |