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  • Bacteria  (1)
  • Brussellator/immobilizer  (1)
  • Springer  (2)
  • American Geophysical Union
  • Geological Society of America (GSA)
  • 2015-2019
  • 1995-1999  (2)
  • 1950-1954
Collection
Publisher
  • Springer  (2)
  • American Geophysical Union
  • Geological Society of America (GSA)
Years
  • 2015-2019
  • 1995-1999  (2)
  • 1950-1954
Year
  • 1
    ISSN: 1432-1416
    Keywords: Turing patterns ; CIMA/starch ; Brussellator/immobilizer ; Schnackenberg/immobilizer model systems ; One-dimensional nonlinear stability analyses
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Mathematics
    Notes: Abstract The development of one-dimensional Turing patterns characteristic of the chlorite-iodide-malonic acid/starch reaction as well as analogous Brussellator/immobilizer and Schnackenberg/immobilizer model systems is investigated by means of a weakly nonlinear stability analysis applied to the appropriately scaled governing equations. Then the theoretical predictions deduced from these pattern formation studies are compared with experimental evidence relevant to the Turing diffusive instabilities under examination in order to explain more fully the transition to such stationary symmetry-breaking spatial structures when the temperature or pool species concentrations vary.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-0603
    Keywords: Adhesin ; Antibody ; Bacteria ; Fab ; Phage display
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Surface proteins provide a multitude of functions for the bacterial cell. Antibodies to these proteins can provide tools for tagging bacteria and characterizing protein function. Phage display technology has emerged as a powerful method for producing monoclonal Fabs in Escherichia coli. In an effort to study the adhesion mechanisms of Streptococcus parasanguis FW213, Fabs specific for the surface adhesin protein Fap1 were produced using phage display. The immune repertoire of a mouse injected with purified Fap1 was cloned into the phagemid vector pCOMB3, and a combinatorial Fab library was expressed in E. coli. A cell-based panning method using whole S. parasanguis cells was developed and has been shown to be a means for enriching for Fabs specific for the Fap1 protein.
    Type of Medium: Electronic Resource
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