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Generic approach

Equation XVII-127 connects the functions 0(F, T), d(Q,P, T) and f Q) and, in principle, if any two are known or can be assumed, the remaining one can be calculated. As may be imagined, many choices of such pairs of functions have been examined, often designed so that Eq. XVII-127 can be handled analytically alternatively, various schemes of successive approximations may be used. The field has become somewhat of a happy hunting ground for physical chemists and there are numerous reviews of the now-extensive literature (see Refs. 144-147 the last is a personalized account). For this reason only some generic approaches will be discussed here. [Pg.656]

Reduction and recycling of waste are inevitably site- and plant-specific, but a number of generic approaches and techniques have been used successfully across the United States to reduce many kinds of industrial wastewaters. [Pg.176]

The drawback of the nitride/Cu(100) approach is its narrow application while the principle is sound, the nanoscale nitride corrals only work on copper and a limited number of other single-crystal surfaces. For more realistic applications, a more generic approach is needed. The obvious place to start is to make use of intermolecular forces to control the arrangement of molecules... [Pg.204]

Figure 5.11. Generic approaches to identify interacting proteins within complexes. The complex is isolated from cells by affinity purification using a tag sequence attached to a protein known to be in the complex. Alternatively, the complex can be immunprecipitated with an antibody to one of the proteins in the complex. The proteins are resolved by polyacrylamide gel electrophoresis, proteolyzed, and the mass of the resulting peptides is determined by mass spectrometry. Alternatively, the proteins can be proteolyzed and the resulting peptides resolved by liquid chromatography. The peptide masses are then determined by mass spectrometry and used for database searching to identify the component proteins. Figure 5.11. Generic approaches to identify interacting proteins within complexes. The complex is isolated from cells by affinity purification using a tag sequence attached to a protein known to be in the complex. Alternatively, the complex can be immunprecipitated with an antibody to one of the proteins in the complex. The proteins are resolved by polyacrylamide gel electrophoresis, proteolyzed, and the mass of the resulting peptides is determined by mass spectrometry. Alternatively, the proteins can be proteolyzed and the resulting peptides resolved by liquid chromatography. The peptide masses are then determined by mass spectrometry and used for database searching to identify the component proteins.
Because the significance of exposure has only been considered over the past few years, there is not as wide a selection of exposure models available as that for fate models. The latter have been applied for several decades to the calculation of ambient exposure levels compared with some standard values. Papers illustrative of human exposure assessments in this symposium include one on airborne pollutant exposure assessments by Anderson (2), a generic approach to estimating exposure in risk studies by Fiksel (5), and a derivation of pollutant limit values in soil or water based on acceptable doses to humans by Rosenblatt, Small and Kainz (6). [Pg.95]

Figure 5 shows the workflow for a generic approach. In order to simplify and structure the exposure assessment of the waste stage, the current assessment approach distinguishes three main waste streams, each of which is connected... [Pg.146]

In Chapter 6 we presented an expression for the transition probability (or intensity, amplitude) of field-swept spectra from randomly oriented simple 5=1/2 systems (Equation 6.4), and we could perhaps tacitly assume (as is generally done in the bioEPR literature) that the expression also holds for effective S = 1/2 systems, such as for the high-spin subspectra defined by the rhombograms discussed in Chapter 5. But what about parallel-mode spectra And how do we compute intensities in complex situations like for systems in the B S B B intermediate-field regime Clearly, we need a more generic approach towards intensity calculations. [Pg.141]

Gill, I. and Ballesteros, A. (1998) Encapsulation of biologicals within silicate, siloxane, and hybrid sol-gel polymers An efficient and generic approach. Journal of the American Chemical Society, 120, 8587-8598. [Pg.108]

The term surface plasmon resonance (SPR) can refer to the phenomenon itself or to the use of this phenomenon to measure biomolecules binding to surfaces. This method is now widely used in the biosciences and provides a generic approach to measurement of bio molecule interactions on surfaces. [Pg.92]

A valuable introduction to the generic approach can be found in literature. To cut down optimization times a good starting point for method development are kit solutions available from a broad range of suppliers. Table 1 is a summary of kit solutions for small molecules from several suppliers. For details on the content of the kit packages please refer to the corresponding supplier. [Pg.98]

P. A. (2000). Generic approach to chiral separations chiral capillary electrophoresis with ternary cyclodextrin mixtures. /. Microcol. Sep. 12, 568 — 576. [Pg.142]

Vassort, A., Barrett, D. A., Shaw, P. N., Ferguson, P. D., and Szucs, R. (2005). A generic approach to the impurity profiling of drugs using standardised and independent capillary zone electrophoresis methods coupled to electrospray ionisation mass spectrometry. Electrophoresis 26, 1712—1723. [Pg.306]

To speed up the lipophilicity determination it was also proposed to use gradient elution procedures (for a review and guidelines, see references [5,101]). This generic approach is particularly useful when series of compounds with a broad lipophilicity range have to be tested since both polar and non-polar solutes can be retained with a reasonable elution time. [Pg.101]

Leonard, P., Hearty, S., Quinn, J., and O Kennedy, R. (2004). A generic approach for the detection of whole Listeria monocytogenes cells in contaminated samples using surface plasmon resonance. Biosens. Bioelectron. 19,1331-1335. [Pg.39]

Zone melting is a possibly generic approach to IL purification. The solidification of ILs often resulfs in the formation of glass. However, it is possible to determine/choose conditions under which single crystals of ILs with a melting point down to -25°C (but not all) can be grown [39]. Where crystallization is seen, then separation of impurities can be demonstrated. [Pg.302]

Three generic approaches for all aflatoxin-susceptible crops could be used to exclude toxigenic fimgi from their environmental niches and to regulate aflatoxin biosynthesis ... [Pg.280]

There are so many different NPs, made by so many different organisms and used in so many ways that it is inevitable that many different goals will be identified but these will usually be based on some generic approaches such as... [Pg.208]

Commonly, new non-covalent MIPs are designed using a generic approach where the functional groups on the binding monomers are chosen according to their complementarity with the chemical groups of the template. In order to... [Pg.6]

For firms that manufacture several products from one source (e.g., Chinese hamster ovary [CHO] cells), a generic approach may suffice. Regulatory authorities in some countries are accepting this approach [13]. There are also some generic kits on the market that can be used to study host cell protein clearance during development, and may be considered acceptable for licensure. [Pg.258]

Our work has been motivated towards making the use of peptide-modified electrodes for detecting metal ions as generic as possible. Essentially, this means developing a generic approach to modifying the electrode so that any peptide can be attached in a manner to provide optimal metal binding capability. [Pg.194]

The generic approach to modifying electrodes with peptides for the detection of metal ions is depicted in Fig. 10.1 and outlined in Procedure 13 (in CD accompanying this book). The essential feature is an electrode modified with an SAM, which contains a carboxylic acid moiety at the distal end. The carboxylic acid moiety is activated using carbodiimides, typically l-ethyl-3-(3-dimethylaminopropyl)... [Pg.195]

Isocratic focusing effects are used to (1) enhance peak shape (2) allow generic approaches to rapid pharmacokinetic screening, (3) perform online concentration for low level metabolite identification, and (4) provide for reducing the amount of... [Pg.335]


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See also in sourсe #XX -- [ Pg.311 ]




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