By Christoph Schnoor (Foreword), Michael Schworer (Foreword), Jochen Decker (Editor), Udo Reischl (Edit
This moment version of a vintage laboratory handbook describes state of the art equipment for the protein-based prognosis of infectious ailments. Explaining the newest advancements in genomics, proteomics, bioinformatics, biosensors, high-throughput units, and recombinant know-how, the authors observe those new methodologies effectively to the id and characterization of priceless diagnostic markers, immunomodulatory elements, epitope mapping, the construction and purification of recombinant antigens, in addition to to diagnostic reagents in immunological assays.
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Extra info for Molecular Diagnosis of Infectious Diseases 2nd Edition (Methods in Molecular Medicine)
R. and Satchidanandam, V. (1996) Analysis of a genomic DNA expression library of Mycobacterium tuberculosis using tuberculosis patient sera: evidence for modulation of host immune response. Infect. Immun. 64, 3765–3771. 5. Chen, X. , Lun, Z. , and Fung, M. C. (2001) High-level expression and purification of immunogenic recombinant SAG1 (P30) of Toxoplasma gondii in Escherichia coli. Protein Expr. Purif. 23, 33–37. 6. Gao, B. and Tsan, M. F. (2003) Endotoxin contamination in recombinant human heat shock protein 70 (Hsp70) preparation is responsible for the induction of tumor necrosis factor alpha release by murine macrophages.
McAdams, H. , Fraser, C. , and Shapiro, L. (2000) Global analysis of the genetic network controlling a bacterial cell cycle. Science 290, 2144– 2148. 8. Schoolnik, G. K. (2002) Microarray analysis of bacterial pathogenicity. Adv. Microb. Physiol. 46, 1–45. 9. Banerjee, N. and Zhang, M. Q. (2002) Functional genomics as applied to mapping transcription regulatory networks. Curr. Opin. Microbiol. 5, 313–317. 10. Conway, T. and Schoolnik, G. K. (2003) Microarray expression profiling: capturing a genome-wide portrait of the transcriptome.
This goal was reached by the combination of isoelectric focusing (IEF) and sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDSPAGE) for two-dimensional electrophoresis (2-DE) (3,4). With this improvement, several hundred proteins were separated within one 2-DE gel. The method was further optimized for high resolution, and at present more than 10,000 protein species may be separated within large (30 × 40 cm) gels (5). In 1995 the term proteome was defined: the proteome refers to the total protein complement of a genome (6).