Cite as: Cold Spring Harb. Protoc.; 2007; doi:10.1101/pdb.prot4608
| Protocol |
This protocol was adapted from "Proteomic Methods for Phosphorylation Site Mapping," Chapter 9, in Proteins and Proteomics (ed. Simpson). Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, USA, 2003.
INTRODUCTION
In this method, microcolumns are prepared using any kind of chromatographic resin. The resin is held in place by making a constriction at the end of a GELoader pipette tip. Sample loading, washing, and elution are performed by loading liquid on top of the resin and applying air pressure to generate a low flow through the column. No frits are necessary.
Related Protocols
This article has been cited by other articles:
![]() |
H. Steen, A. Stensballe, and O. N. Jensen Alkaline Phosphatase Treatment of Phosphopeptides: In-Solution Dephosphorylation prior to MALDI-MS Analysis CSH Protocols, May 1, 2008; 2008(6): pdb.prot4610 - pdb.prot4610. [Abstract] [Full Text] |
||||
![]() |
H. Steen, A. Stensballe, and O. N. Jensen Alkaline Phosphatase Treatment of Phosphopeptides: In-Solution Dephosphorylation after MALDI-MS Analysis CSH Protocols, May 1, 2008; 2008(6): pdb.prot4611 - pdb.prot4611. [Abstract] [Full Text] |
||||
Copyright © 2007 by Cold Spring Harbor Laboratory Press. Online ISSN: 1559-6095 Terms of Service |