GPM #: Keyword: # GPM # proteins Description 1. GPM77711002533 peptide model gel aaa go mh 2576 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: CDC23, unlabelled, trypsin cleavage, spectrum name 20090616_Orbi2_NiHu_SA_FLP_CDC231_090617203217.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 2. GPM77711002534 peptide model gel aaa go mh 2484 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: CDC23, unlabelled, trypsin cleavage, spectrum name 20090616_Orbi2_NiHu_SA_FLP_CDC232_090617230411.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 3. GPM77711002535 peptide model gel aaa go mh 2661 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: CDC23, unlabelled, trypsin cleavage, spectrum name 20090616_Orbi2_NiHu_SA_FLP_CDC233_090618013546.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 4. GPM77711002536 peptide model gel aaa go mh 2492 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: CDC23, unlabelled, trypsin cleavage, spectrum name 20090616_Orbi2_NiHu_SA_FLP_HeLa1_090617125629.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 5. GPM77711002537 peptide model gel aaa go mh 2367 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: CDC23, unlabelled, trypsin cleavage, spectrum name 20090616_Orbi2_NiHu_SA_FLP_HeLa2_090617152832.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 6. GPM77711002538 peptide model gel aaa go mh 2709 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: CDC23, unlabelled, trypsin cleavage, spectrum name 20090616_Orbi2_NiHu_SA_FLP_HeLa3_090617180004.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 7. GPM77711002540 peptide model gel aaa go mh 1401 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: CDC23, SILAC labelled, endoLysC cleavage, spectrum name 20090616_Orbi2_NiHu_SA_FLP_CDC23_L.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 8. GPM77711002542 peptide model gel aaa go mh 2363 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: CDC23, SILAC labelled, trypsin cleavage, spectrum name 20090806_Orbi2_NiHu_SA_FLP_CDC23heavy_2.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 9. GPM77711002543 peptide model gel aaa go mh 2882 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: Pericentrin, unlabelled, trypsin cleavage, spectrum name 20090727_Orbi2_NiHu_SA_FLP_0023_PcA1.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 10. GPM77711002544 peptide model gel aaa go mh 2765 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: Pericentrin, unlabelled, trypsin cleavage, spectrum name 20090727_Orbi2_NiHu_SA_FLP_0023_PcA2.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 11. GPM77711002545 peptide model gel aaa go mh 2607 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: Pericentrin, unlabelled, trypsin cleavage, spectrum name 20090727_Orbi2_NiHu_SA_FLP_0023_PCA3.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 12. GPM77711002546 peptide model gel aaa go mh 2630 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: Pericentrin, unlabelled, trypsin cleavage, spectrum name 20090727_Orbi2_NiHu_SA_FLP_0023_PcB1.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 13. GPM77711002547 peptide model gel aaa go mh 2490 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: Pericentrin, unlabelled, trypsin cleavage, spectrum name 20090727_Orbi2_NiHu_SA_FLP_0023_PcB2.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 14. GPM77711002548 peptide model gel aaa go mh 2755 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: Pericentrin, unlabelled, trypsin cleavage, spectrum name 20090727_Orbi2_NiHu_SA_FLP_0023_PcB3.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 15. GPM77711002549 peptide model gel aaa go mh 2640 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: Pericentrin, unlabelled, trypsin cleavage, spectrum name 20090727_Orbi2_NiHu_SA_FLP_0023_TDS1.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 16. GPM77711002550 peptide model gel aaa go mh 2705 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: Pericentrin, unlabelled, trypsin cleavage, spectrum name 20090727_Orbi2_NiHu_SA_FLP_0023_TDS2.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 17. GPM77711002551 peptide model gel aaa go mh 2439 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: Pericentrin, unlabelled, trypsin cleavage, spectrum name 20090727_Orbi2_NiHu_SA_FLP_0023_TDS3.RAW. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 18. GPM77711002552 peptide model gel aaa go mh 3486 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: TACC3, unlabelled, trypsin cleavage, spectrum name 20090619_Velos4_NiHu_SA_FLP_TACCmutTAC.raw. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 19. GPM77711002553 peptide model gel aaa go mh 3904 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: TACC3, unlabelled, trypsin cleavage, spectrum name 20090619_Velos4_NiHu_SA_FLP_TACCwtTAC.raw. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . 20. GPM77711002554 peptide model gel aaa go mh 3852 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry name: Hubner NC, et al. project: Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions project comment: Tranche  Published in Hubner NC, Bird AW, Cox J, Splettstoesser B, Bandilla P, Poser I, Hyman A, Mann M. J Cell Biol. 2010 May 17;189(4):739-54 (PubMed). Data folder: TACC3, unlabelled, trypsin cleavage, spectrum name 20090619_Velos4_NiHu_SA_FLP_U2OSTAC.raw. From the abstract: In this study, we show that combining bacterial artificial chromosome (BAC) TransgeneOmics with quantitative interaction proteomics, which we call quantitative BAC-green fluorescent protein interactomics (QUBIC), allows specific and highly sensitive detection of interactions using rapid, generic, and quantitative procedures with minimal material. . Page 1 of 4 | 1 | 2 | 3 | 4 | Key word(s): 20479470 Total protein ids = 153593 If you do not see a red dot in the square brackets [], you will need Adobe's SVG plugin to view this site properly.

dblist_gpmnotes.pl, v. 2010.07.06