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Proteomics analysis

Lu B, Soreghan BA, Thomas SN, Chen T, Yang AJ. Towards global proteomic analysis in a PSl/APP mouse of Alzheimer s disease. ACS. San Diego, 2005. [Pg.160]

Meier, B. W. Gomez, J. D. Zhou, A. Thompson, J. A. Immunochemical and proteomic analysis of covalent adducts formed by quinone methide tumor promoters in mouse lung epithelial cell lines. Chem. Res. Toxicol. 2005, 18, 1575-1585. [Pg.352]

Hancock, W., Apffel, A., Chakel, J., Hahnenberger, K., Choudhary, G., Traina, J.A., and Pungor, E., Integrated genomic/proteomic analysis, Anal. Chem. News Reports, 71(21), 742A, 1999. [Pg.70]

Chen, M.-L. Chen, C.-H. (2005a). Comparative proteome analysis revealed up-regulation of transthyretin in rat brain under chronic clozapine treatment. /. Psychiatric Res., 41(1/2), 63-8. [Pg.166]

Aicher, L., Wahl, D., Arce, A., Grenet, O., and Steiner, S. (1998). New insights into cyclosporine A nephrotoxicity by proteome analysis. Electrophoresis 19, 1998-2003. [Pg.111]

Gygi, S. P., Corthals, G. L., Zhang, Y., Rochon, Y., and Aebersold, R. (2000). Evaluation of two-dimensional gel electrophoresis-based proteome analysis technology. Proc. Natl. Acad. Sci. USA 97, 9390-9395. [Pg.114]

Soskic, V., Gorlach, M., Poznanovic, S., Boehmer, F. D., and Godovac-Zimmermann, J. (1999). Functional proteomics analysis of signal transduction pathways of the platelet-derived growth factor b receptor. Biochemistry 38, 1757-1764. [Pg.122]

Williams, C., and Addona, T. A. (2000). The integration of SPR biosensors with mass spectrometry possible applications for proteome analysis. Trends Biotechnol. 18, 45-48. [Pg.123]

Proteome Analysis Protocols. Totowa, NJ Humana Press, 1999. [Pg.224]

Griffin, T. J. Han, D. K. Gygi, S. R Rist, B. Lee, H. Aebersold, R. Parker, K. C. Toward a high-throughput approach to quantitative proteomic analysis Expression-dependent protein identification by mass spectrometry. J. Am. Soc. Mass. Spectrom. 2001,12,1238-1246. [Pg.225]

Fulda, S., S. Mikkat, F. Huang et al. (2006). Proteome analysis of salt stress response in the cyanobacterium Synechocystis sp. strain PCC 6803. Proteomics 6(9) 2733-2745. [Pg.15]

Crabb, JW, Miyagi, M, Gu, X, Shadrach, K, West, KA, Sakaguchi, H, Kamei, M, Hasan, A, Yan, L, Raybom, ME, Salomon, RG, and Hollyfield, JG, 2002. Drusen proteome analysis an approach to the etiology of age-related macular degeneration. Proc Natl Acad Sci USA 99, 14682-14687. [Pg.341]

Mann, M., Jensen, O.L. (2003). Proteomic analysis of post-translational modifications. Nature Biotech. 21, 255. [Pg.89]

Polymer monolithic columns with small diameter have been successfully employed for proteome analysis. Karger and coworkers reported MALDI-TOF of separated fractions spotted on a plate from a polymeric reversed-phase column that showed high peak capacity (Chen et al., 2005). Huber and coworkers reported separation and detection of about 200 peaks within 5 min by using a PSDVB column (Premstaller et al., 2001). [Pg.152]

Chen, H.S., Rejtar, T., Andreev, V., Moskovets, E., Karger, B.L. (2005). High-speed, high-resolution monolithic capillary LC-MALDI MS using an off-line continuous deposition interface for proteomic analysis. Anal. Chem. 77, 2323-2331. [Pg.171]

Schley, C., Altmeyer, M.O., Swart, R., Muller, R., Huber, C.G. (2006). Proteome analysis of Myxococcus xanthus by off-line two-dimensional chromatographic separation using monolithic poly-(styrene-divinylbenzene) columns combined with ion-trap tandem mass spectrometry. J. Proteome Res. 5, 2760-2768. [Pg.175]

Hoffmann, R, Ji, H., Moritz, R. L., Connolly, L. M., Frecklington, D. F., Layton, M. J., Eddes, J. S., Simpson, R. J. (2001). Continuous free-flow electrophoresis separation of cytosolic proteins from the human colon carcinoma cell line LIM 1215 a non two-dimensional gel electrophoresis-based proteome analysis strategy. Proteomics 1(7), 807. [Pg.239]

Proteomic analysis and identification of new hiomarkers and therapeutic targets for invasive ovarian cancer. Proteomics 2(1), 76-84. [Pg.240]

Adkins, J.N., Vamum, S.M., Auberry, K.J., Moore, R.J., Angell, N.H., Smith, R.D., Springer, D.L., Pounds, J.G. (2002). Toward a human blood serum proteome analysis by multidimensional separation coupled with mass spectrometry. Mol. Cell. Proteomics 1,47-955. [Pg.255]

Chen, J., Balgley, B.M., DeVoe, D.L., Lee, C.S. (2003a). Capillary isoelectric focusing-hased multidimensional concentration/separation platform for proteome analysis. Anal. Chem. [Pg.256]

Skipp, P., Robinson, J., O Connor, C.D., Clarke, I.N. (2005). Shotgun proteomic analysis of Chlamydia trachomatis. Proteomics 5, 1558-1573. [Pg.258]

Vollmer, M., Nagele, E., Horth, P. (2003). Differential proteome analysis two-dimensional nano-LC/MS of E. coli proteome grown on different carbon sources. J. Biomol. Tech. 14, 128-135. [Pg.259]

Wenner, B.R., Lovell, M.A., Lynn, B.C. (2004). Proteomic analysis of human ventricular cerebrospinal fluid from neurologically normal, elderly subjects using two-dimensional LC-MS/MS. J. Proteome Res. 3, 97-103. [Pg.259]

The enormous dynamic range of proteins in the sample represents an additional difficulty in proteome analysis. The best example is semm with a protein abundance ranging over eleven orders of magnitude (Anderson and Anderson, 2002). To detect the low abundant species, one has to load a sufficient amount of digest on a column to meet the limit of detection (LOD) of the MS instrument. Some reports published used up to 2.5 L of plasma with an extensive fractionation of intact proteins prior to LC-MS analysis on the peptide level (Rose et al., 2004). [Pg.282]


See other pages where Proteomics analysis is mentioned: [Pg.1027]    [Pg.1030]    [Pg.147]    [Pg.396]    [Pg.221]    [Pg.29]    [Pg.148]    [Pg.219]    [Pg.224]    [Pg.225]    [Pg.5]    [Pg.30]    [Pg.7]    [Pg.122]    [Pg.160]    [Pg.207]    [Pg.209]    [Pg.210]    [Pg.248]    [Pg.254]    [Pg.254]    [Pg.255]    [Pg.257]    [Pg.261]    [Pg.264]    [Pg.276]   
See also in sourсe #XX -- [ Pg.1343 ]




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