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Affine functions

Capture array involves the immobilization of non-protein molecules onto the surface which can interact with proteins in the solute phase. Generally, capture molecules may be broad capture agents based on chromatography type surface chemistries such as ion exchange, hydrophobic and metal affinity functionality, or they may be highly specific such as molecular imprinted polymers or oligonucleotide aptamers. [Pg.360]

A self-affine fractal profile with dFsR =1.5 was obtained by taking a, b, and N as 0.8165, 1.5, and 50, respectively. Next, various affine functions h(x) were made by multiplying /ws (x)... [Pg.372]

Affinities/functional activities at relevant molecular targets Pharmacological profiling — binding or functional assays at receptors, enzymes, ion channels, transporters Wakefield et al.,-83 Bowes et al.20... [Pg.257]

Affinities/functional activities at relevant molecular targets... [Pg.260]

Affinities/functional activities Pharmacological profiling — Bowes et al. 20 Wakefield et al. 83... [Pg.263]

Expression analysis using DNA microarrays analyzes only the transcriptome it should be mentioned that mRNA abundance in a cell often correlates poorly with the amount of protein synthesized (27). Important regulation takes place at the levels of translation and enzymatic activities. The only effect of a signal transduction pathway that is observed in a gene expression experiment is that at the endpoint of a given pathway. DNA microarrays currently have little value in determining post-translational modifications, which influence the diversity, affinity, function, cellular abundance, and transport of proteins. [Pg.30]

A number of specific components contribute to the complex energetics of lectin-ligand interactions. The observed affinities (functional affinities, see Section ll.B.l)... [Pg.221]

The first member of relation 9.19 is therefore an affinity function of the ratio of absorbances figuring in the second member. The calculated values are on a straight line whose slope and intercept enable calculations to be made for and Cj,. [Pg.196]

Early modeling efforts focused on equilibrium and near equilibrium conditions. Olander (J 3) developed analytical solutions for a variety of reaction shemes under reaction equilibrium conditions. Friedlander and Keller (44) used an affinity function to obtain analytical solutions for systems near reaction equilibrium. Secor and Beutler (45) used penetration theory to calculate transient mass transfer by numerical methods. Their results for semi-infinite media can be used for short time results. [Pg.12]

Improvement function G2 The second improvement function, G2, is a deterministic linear strictly decreasing function, see Fig. 2. It satisfies the following properties G2(0) = G m and G2(T) = Gmin = 0. This improvement function G2 is an affine function and its equation is defined by the following formula ... [Pg.559]

FOR-statements in which the upper and lower bound expressions are affine functions on the loop iterators. [Pg.80]

Furthermore, let I be an index vector containing loop iterators and let /(/) be an affine function on I. Then all variables of the program are of the form... [Pg.80]

Friedlander, S.K. and K.H. Keller. "Mass transfer in reacting systems near equilibrium. Use of the affinity function." Chemical Engineering Science 20 (1965) 121-129. [Pg.379]

The definition of self-similarity is based on the property of equal magnification in all directions. However, there are many objects in nature which have unequal scaling in different directions. Thus these are not self-similar but self-affine. The dimension of self-affine fractals cannot be obtained from Equation 5.5, which is based on the self-similarity of an object. Mandelbrot showed that the lengths of self-affine fractal curves do not follow the relation L 6 ° for all values of e and therefore the dimension of self-affine curves cannot be obtained by measuring their lengths. Instead, the dimension of self-affine functions can be obtained from their power spectra. [Pg.171]

To be qualified as a CWA simulant, the chemical should ntimic the behavior of the CWA it simulates. It must be relatively nontoxic if the simulant is intended for outdoor dissemination. The chosen substance must be environmentally benign. If the simulant is intended for use under laboratory control conditions, substances with some toxicity can be used. Simulants are chosen based on structural, vapor pressure function group similarities to respective CWAs. When the simulant is used to evaluate detector performance, choosing the simulant that closely matches the type of detection methodology used by the detector is of the utmost importance. For example, if the detection device is an ion mobility detector, the simulant chosen must have similar ionization affinity, function group, and structure size so that its mobility is similar to the CWA. [Pg.100]

We considered a binary representation with 30 bits per antibody corresponding to a large search space. Then we had to define an affinity function. As suggested in Section 4, we considered two factors to compute this function. The first factor represents the quality of the antibody, given by the function / we aim to optimize. The second factor represents the correlation between an antibody and any other antibody of the population, for this we used the Hamming distance between the two antibody strings u and v of size m... [Pg.145]

As second example we considered the Iterated Prisoner s Dilemma. The aim of this example is to show the use of the Algorithm with a less trivial problem, and the use of more sophisticated antibody representation and affinity function. [Pg.145]

The training data set and the test data set should be scaled before processing. The sample will be standardized to the range of 0.0 to 1.0 using an affine function. [Pg.316]

There are often differences in binding affinity, functional activity and/or pharmacological activity across species. Although interspecies potency differences are seen with other biological molecules, such as interleukins and interferons, MAbs often show absolute species specificity because they are restricted to binding a single epitope. [Pg.110]


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See also in sourсe #XX -- [ Pg.150 ]




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