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Availability binding

The Deficit Reduction Act of 1984 significandy curtailed the available binding for the USSEC, which ceased operations in 1985. [Pg.356]

High yields are possible due to the large capacity of the ChiraLig for the single enantiomer on each load cycle. A significant percentage of the available binding sites are used in each cycle to bind the eutomer. [Pg.210]

Many neurotransmitters are inactivated by a combination of enzymic and non-enzymic methods. The monoamines - dopamine, noradrenaline and serotonin (5-HT) - are actively transported back from the synaptic cleft into the cytoplasm of the presynaptic neuron. This process utilises specialised proteins called transporters, or carriers. The monoamine binds to the transporter and is then carried across the plasma membrane it is thus transported back into the cellular cytoplasm. A number of psychotropic drugs selectively or non-selectively inhibit this reuptake process. They compete with the monoamines for the available binding sites on the transporter, so slowing the removal of the neurotransmitter from the synaptic cleft. The overall result is prolonged stimulation of the receptor. The tricyclic antidepressant imipramine inhibits the transport of both noradrenaline and 5-HT. While the selective noradrenaline reuptake inhibitor reboxetine and the selective serotonin reuptake inhibitor fluoxetine block the noradrenaline transporter (NAT) and serotonin transporter (SERT), respectively. Cocaine non-selectively blocks both the NAT and dopamine transporter (DAT) whereas the smoking cessation facilitator and antidepressant bupropion is a more selective DAT inhibitor. [Pg.34]

An additional question relating to sites of modification is the possible influence of DNA binding proteins and the conformational changes they induce in DNA as it forms chromatin, which in turn may influence available binding sites for adduct formation. Several studies have investigated the distribution of DNA adducts in chromatin (95-102). although no clear answer for the influence of these proteins has yet emerged. [Pg.201]

The basis for this technique lies in the competition between the test antigen and a labelled antigen for the available binding sites on a fixed amount of antibody. While the binding sites are traditionally associated with an antibody, any source of specific reversible binding sites may be used to create an assay in this format. Examples of such are specific transport proteins such as thyroxine-binding globulin and certain cellular receptors such as opiate or benzodiazepine receptors. Under these circumstances the equilibrium mixture may be represented thus ... [Pg.245]

The solutions to Equation 9 are those values of g for which the functional f=(l- ) intersects the functional f=(l-ag), where r=fcn[CQ,k, k, nQ,eQ,k, k ] and a in general also is a function of the same variables. Actin binding protein (ABP) joins contiguous chains and a therefore depends on strand density and network topology in addition to the intrinsic rate constants for attachment of ABP to an available binding site. [Pg.228]

Only nonpolar solvents, e.g., cyclohexane (most commonly employed with silica gel and silicic acid), methylcyclohexane, methylpentane, and carbon tetrachloride, can be utilized in these slurries since solvents of greater polarity will compete with the intended adsorbate for available binding sites and will result in incomplete sustrate adsorption. [Pg.316]

Further insight into molecular binding to the solid surface is possible from a determination of the surface area occupied by each molecule in a mono-layer. In a detailed study of the adsorption of a range of substances on silica gel (surface area 200 m2/g), Weis and coworkers9 found that a relatively small number of polynuclear aromatic substances occupied all available binding sites, indicating that the molecules are oriented parallel to the solid surface to... [Pg.318]

The stability of modern volatile agents is the result of the heavy fluorination of the ether molecule. The effect is most pronounced for CF3 and CF2 moieties. In the case of desflurane, of the eight available binding sites for halogens, six are occupied by fluorine atoms. Similarly, sevoflurane has seven fluorine atoms out of a possible ten. The lack of hydrogen atoms reduces both flammability and potency. [Pg.55]

A) The protein conformation does or does not provide access to the protein interior for the surfactant molecules, with implications for the number of available binding sites on each protein. [Pg.177]

Supramolecular control of reactivity and catalysis is among the most important functions in supramolecular chemistry. Since catalysis arises from a differential binding between transition and reactant states, a supramolecular catalyst is, in essence, chemical machinery in which a fraction of the available binding energy arising from noncovalent interactions is utilized for specific stabilization of the transition state or, in other words, is transformed into catalysis. [Pg.113]

Fabbrizzi and coworkers reported the synthesis of dicopper(II) complexes of bis-tren cryptands 61-63. The metal center was coordinated by a tren subunit oriented to a trigonal bipyramidal geometry which had an available binding site for anions at a vacant axial position. The complex 61 [49] showed the highest... [Pg.184]

Figure 10. Proposed Adaptation of a Fluorescence Energy Transfer Immunoassay to the Microparticle Sensor Design. A mixture of two different microparticles, each containing different reagents, are entrapped physically in the polyacrylamide layer. The reagents released from the microparticles set up a competition reaction between the free and labeled antigens for the available binding sites of labeled-antibody. The immunocomplexes formed have different emission spectra, allowing quantitation of free antigen concentration. Figure 10. Proposed Adaptation of a Fluorescence Energy Transfer Immunoassay to the Microparticle Sensor Design. A mixture of two different microparticles, each containing different reagents, are entrapped physically in the polyacrylamide layer. The reagents released from the microparticles set up a competition reaction between the free and labeled antigens for the available binding sites of labeled-antibody. The immunocomplexes formed have different emission spectra, allowing quantitation of free antigen concentration.
Displacement segregation involves another component in a formulation competing for the available binding sites on the carriers, thus displacing some adhering dmg particles. [Pg.168]

Saturation segregation involves any excess fine particles with no available binding sites on carrier particles. Formulations with excessive dmg loading act this way in certain circumstances. [Pg.168]


See other pages where Availability binding is mentioned: [Pg.72]    [Pg.225]    [Pg.44]    [Pg.86]    [Pg.410]    [Pg.285]    [Pg.285]    [Pg.387]    [Pg.105]    [Pg.9]    [Pg.246]    [Pg.83]    [Pg.32]    [Pg.669]    [Pg.223]    [Pg.392]    [Pg.163]    [Pg.383]    [Pg.118]    [Pg.1051]    [Pg.245]    [Pg.245]    [Pg.5]    [Pg.6]    [Pg.7]    [Pg.163]    [Pg.55]    [Pg.406]    [Pg.225]    [Pg.521]    [Pg.752]    [Pg.166]    [Pg.6]    [Pg.368]    [Pg.314]   
See also in sourсe #XX -- [ Pg.17 , Pg.19 , Pg.20 , Pg.23 ]




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