Open Access Highly Accessed Methodology article

From an electrophoretic mobility shift assay to isolated transcription factors: a fast genomic-proteomic approach

Astrid R Mach-Aigner1, Karin Grosstessner-Hain3, Marcio J Poças-Fonseca2, Karl Mechtler3 and Robert L Mach1*

Author Affiliations

1 Gene Technology, Department of Gene Technology and Applied Biochemistry, Institute of Chemical Engineering, TU Wien, Getreidemarkt 9/166/5/2, A-1060 Wien, Austria

2 Department of Genetics and Morphology, Institute of Biological Sciences, University of Brasilia, Campus Universitário Darcy Ribeiro, ICC SuL, AT-098, 70.910-900, Brasília-DF, Brazil

3 Research Institute of Molecular Pathology, Vienna Biocenter, Dr. Bohrgasse 7, A-1030 Vienna, Austria

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BMC Genomics 2010, 11:644  doi:10.1186/1471-2164-11-644

Published: 18 November 2010

Additional files

Additional file 1:

List of H. jecorina proteins identified by tandem MS analysis. The corresponding proteomic data are available at the publically available database https://proteomecommons.org/ webcite.

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Additional file 2:

Multiple sequence alignment of the H. jecorina 2488prp with hypothetical proteins of other fungi, namely Nectria haematococca (GeneID: 9678588), Gibberella zeae (GeneID: 2791570), Neurospora crassa (GeneID: 3874038), Podospora anserina (GeneID: 6189947) Chaetomium globosum (GeneID: 4395593), Magnaporthe grisea (GeneID: 2675104).

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