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Coupling segments

The earliest and simplest approach in this direction starts from Langevin equations with solutions comprising a spectrum of relaxation modes [1-4], Special features are the incorporation of entropic forces (Rouse model, [6]) which relax fluctuations of reduced entropy, and of hydrodynamic interactions (Zimm model, [7]) which couple segmental motions via long-range backflow fields in polymer solutions, and the inclusion of topological constraints or entanglements (reptation or tube model, [8-10]) which are mutually imposed within a dense ensemble of chains. [Pg.3]

DCC or EDC with an additive This is probably the most common method of coupling segments, with HOBt and HOObt competing as the most efficient additives. HOAt may be on par with the other two. The additive is essential to reduce isomerization to acceptable levels (see Sections 2.25 and 2.26). An important variant is supplementation of the reaction mixture with a cupric ion that minimizes or eliminates isomerization by preventing any oxazolone that is formed from enolizing (see Section 7.2). [Pg.59]

Dubrulle J, Pourquie O. (2004) Coupling segmentation to axis formation. [Pg.147]

Dubrulle, J., and O. Pourquie. 2004. Coupling Segmentation to Axis Formation. Development 131, no 23 5783-93. [Pg.22]

The choice of the vector d is very important for the exploitation of cooccurrence matrix. For segmentation operation, d will be calculated with the result that could separate the noise of defects. We will have therefore to research transitions to frontiers, that is to say couples (i, j) such that i is an intensity linked to the noise and j an intensity linked to the defect. [Pg.234]

This last factor overcounts the number of couplings, since the random placement of chain segments makes it improbable that each entanglement will involve a new molecule. Thus an entanglement may be redundant the chain might already be coupled to the original molecule. [Pg.118]

Several human receptors for the neurohypophyseal hormones have been cloned and the sequences elucidated. The human V2 receptor for antidiuretic hormone presumably contains 371 amino acids and seven transmembrane segments and activates cycHc AMP (76). The oxytocin receptor is a classic G-protein-coupled type of receptor with a proposed membrane topography also involving seven transmembrane components (84). A schematic representation of the oxytocin receptor stmcture within the membrane is shown in Eigure 4 (85). [Pg.191]

In a variation of this process, polymerization can start in the center (B segment, and A segments can then be polymerized onto each end. Alternatively, can be joined together by a coupling agent ... [Pg.14]

Sulphate in Waters, Effluents and Solids (2nd Edition) [including Sulphate in Waters, Effluents and Some Solids by Barium Sulphate Gravimetry, Sulphate in waters and effluents by direct Barium Titrimetry, Sulphate in waters by Inductively Coupled Plasma Emission Spectrometry, Sulphate in waters and effluents by a Continuous Elow Indirect Spectrophotometric Method Using 2-Aminoperimidine, Sulphate in waters by Elow Injection Analysis Using a Turbidimetric Method, Sulphate in waters by Ion Chromatography, Sulphate in waters by Air-Segmented Continuous Elow Colorimetry using Methylthymol Blue], 1988... [Pg.315]

Schreiner etal. (2001) modelled the precipitation process of CaC03 in the SFTR via direct solution of the coupled mass and population balances and CFD in order to predict flow regimes, induction times and powder quality. The fluid dynamic conditions in the mixer-segmenter were predicted using CFX 4.3 (Flarwell, UK). [Pg.258]

The choice of what protective groups to use in the synthesis of each segment was based on three aspects (a) the specific steps chosen to achieve the synthesis of each segment (b) the methods to be used in coupling the various segments, and (c) the conditions needed to deprotect the 42 blocked groups in order to... [Pg.11]


See other pages where Coupling segments is mentioned: [Pg.267]    [Pg.284]    [Pg.284]    [Pg.70]    [Pg.794]    [Pg.229]    [Pg.361]    [Pg.361]    [Pg.1470]    [Pg.74]    [Pg.372]    [Pg.211]    [Pg.267]    [Pg.284]    [Pg.284]    [Pg.70]    [Pg.794]    [Pg.229]    [Pg.361]    [Pg.361]    [Pg.1470]    [Pg.74]    [Pg.372]    [Pg.211]    [Pg.2554]    [Pg.118]    [Pg.173]    [Pg.531]    [Pg.94]    [Pg.360]    [Pg.549]    [Pg.74]    [Pg.505]    [Pg.514]    [Pg.1915]    [Pg.5]    [Pg.5]    [Pg.6]    [Pg.6]    [Pg.6]    [Pg.879]    [Pg.484]    [Pg.702]    [Pg.11]    [Pg.12]    [Pg.12]    [Pg.12]   
See also in sourсe #XX -- [ Pg.242 ]




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Options for Minimizing Epimerization during the Coupling of Segments

Peptide segment coupling

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