References
- Adams, M. D., S. E. Celniker, R. A. Holt, et al. 2000. The genome sequence of Drosophila melanogaster. Science 287, 2185-2195 https://doi.org/10.1126/science.287.5461.2185
- Baggerman G., A. Cerstiaens, A. De Loof, and J. Schoofs. 2002. Peptidornics of the larval Drosophila melanogaster central nervous system. J. BioI. Chem. 277, 40368-40374 https://doi.org/10.1074/jbc.M206257200
- Bossie, C. A. and M. M. Sanders. 1993. A cDNA from Drosophila melanogaster encodes a lamin C-like intermediate filament protein. J. Cell Sci. 104, 1263-1272
- Bradford, M. M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72, 248-254 https://doi.org/10.1016/0003-2697(76)90527-3
- Ericsson, C., Z. Petho, and H. Mehlin. 1997. An on-line two-dimensional polyacrylamide gel electrophoresis protein database of adults Drosophila melanogaster. Electrophoresis 18, 484-490 https://doi.org/10.1002/elps.1150180324
- Giot, I., J. S. Bader, C. Brouwer, et al. 2003. A protein interaction map of Drosophila melanogaster. Science 302, 1727-1736 https://doi.org/10.1126/science.1090289
- Gong, I., M. Purl, M. Unlu, M. Young, K. Robertson, S. Viswanathan, A. Krishnaswamy, S. R. Dowd, and J. S. Minden. 2004. Drosophila ventral furrow morphogenesis: a proteomic analysis. Development 131, 643-656 https://doi.org/10.1242/dev.00955
- Gorg, A., W. Postel, S. Gunther, J. Weser, J. R. Strahler, S. M. Hanash, J. Somerlat, and R. Kuick. 1988. Approach to stationary two-dimensional pattern: influence of focusing time and immobilinel carrier ampholytes concentrations. Electrophoresis 9, 37-46 https://doi.org/10.1002/elps.1150090108
- Heukeshoven, J. and R. Dernick. 1988. Improved silver staining procedure for fast staining in PhastSystem Development Unit. J. Staining of sodium dodecyl sulfate gels. Electrophoresis 9, 28-32 https://doi.org/10.1002/elps.1150090106
- http://www.proteinprospector.ucsf.edu
- Laemmli, U. K. 1970. Oeavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227, 680-685 https://doi.org/10.1038/227680a0
- Langen, H., C. Gray, D. Roder, J. F. Juranville, B. Takacs, and M. Fountoulakis. 1997. From genome to proteome: protein map of Haemophilus injluenzae. Electrophoresis 18, 1184-1192 https://doi.org/10.1002/elps.1150180727
- Messina, A, M. Neri, F. Perosa, C. Caggese, M. Marino, R. Caizzi, and V. De Pinto. 1996. Cloning and chromosomal localization of a cDNA encoding a mitochondrial porin from Drosophila melanogaster. FEBS Letter. 384, 9-13 https://doi.org/10.1016/0014-5793(96)00268-2
- O'Connell, K. J. and J. T. Stults. 1997. Identification of mouse liver proteins on two-dimensional electrophoresis gels by matrix-assisted laser desorption/ionization mass spectrometry of in situ enzymatic digests. Electrophoresis 18, 349-359 https://doi.org/10.1002/elps.1150180309
- Ordway, R. W., J. Pallanck, and B. Ganetzky. 1994. Neurally expressed Drosophila encoding homologs for the NSF and SNAP secretory proteins. Proc. Natl. Acad. Sci. USA. 91, 5715-5719
- Quadroni, M. and P. James. 1999. Proteomics and automation. Electrophoresis 20, 664-677 https://doi.org/10.1002/(SICI)1522-2683(19990101)20:4/5<664::AID-ELPS664>3.0.CO;2-A
- Shevchenko, A, M. Wilm, O. Vorm, and M. Mann. 1996. Mass spectrometric sequencing of proteins from silverstained polyacrylamide gels. Anal. Chem. 68, 850-858 https://doi.org/10.1021/ac950914h
- Talluri, S., A Bhatt, and D. P. Smith. 1995. Identification of a Drosophila G protein a subunit (dGqa-3) expressed in chemosensory cells and central neurons. Proc. Natl. Acad. Sci. USA. 92, 11475-11479
- Theurkauf, W. E., H. Baum, J. Bo, and P. C. Wensink. 1986. Tissue-specific and constitutive alpha-tubulin genes of Drosophila melanogaster code for structurally distinct proteins. Proc. Natl. Acad. Sci. USA. 83, 8477-8481
- Vierstraete, E., A Cerstiaens, G. Baggerman, G. Van den Bergh, A De Loof, and J. Schoofs. 2003. Proteomics in Drosophila melanogaster: first 2D database of larval hemolymph proteins. Biochem. Biophys. Res. Commun. 304, 831-838 https://doi.org/10.1016/S0006-291X(03)00683-1
- Vierstraete, E., P. Verleyen, G. Baggerman, W. D'Hertog, G. Van den Bergh, J. Arckens, A De Loof, and J. Schoofs. 2004. A proteomic approach for the analysis of instantly released wound and immune proteins in Drosophila rnelanogaster hemolymph. Proc. Natl. Acad. Sci. USA. 101, 470-475
- Weekes, J., C. H. Wheeler, J. X. Yan, J. Weil, T. Eschenhagen, G. Scholtysik, and M. J. Dunn. 1999. Bovine dilated cardiomyopathy: proteomic analysis of an animal model of human dilated cardiomyopathy. Electrophoresis 20, 898-906 https://doi.org/10.1002/(SICI)1522-2683(19990101)20:4/5<898::AID-ELPS898>3.0.CO;2-B
- Wilkins, M. R., C. Pasquali, R. D. Appel, K. au, O. Golaz, J. C. Sanchez, J. X. Yan, A A Gooley, G. Hughes, J. Humphery-Smith, K. J. Williams, and D. F. Hochstrasser. 1996. From proteins to proteomes: large scale protein identification by two-dimensional electrophoresis and amino acid analysis. Biotechnology 14, 61-65 https://doi.org/10.1038/nbt0196-61