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Potential step methods technique types

Again, application of the principle to the simple potential-step method appears trivial or superfluous. However, it is of quite great important for other types of potential control, namely double potential step, cyclic potential step [73], and especially the linear potential sweep method [21, 22, 73]. In all these techniques, sets of data Jf ( ) /f (f) E can be obtained, thus enabling kt(E) to be determined from eqn. (100). For more details, the reader is referred to the quoted textbooks. [Pg.267]

Whilst ec reactions as described by Equations (2.60) and (2.61) may sometimes be studied by single potential step methods, the double potential step technique is greatly preferred, i.e. a waveform of the type shown in Fig. 2.11 is applied to the working electrode. [Pg.64]

It may be emphasized here that such an elaboration is possible for any small amplitude perturbation technique. It is only necessary to explicitize either the first-order current or the first-order interfacial potential, corresponding to the type of perturbation, to be able to derive expressions for 7q, 1 and AEl. So, the treatment is also useful to estimate the error due to second-order non-linearity in the step methods. However, a separate measurement of the second-order effect can only be done with (sinusoidal) a.c. perturbation. In Table 5, the explicit expressions for SF pertaining to the four methods mentioned in Sect. 2.4.1 are given in such a way that the connection between them is clearly shown. [Pg.258]

In principle, mesoscale methods can provide a means for connecting one type of simulation to another. For example, a molecular simulation can be used to describe a lipid. One can then derive the parameters for a lipid-lipid potential. These parameters can then be used in a simulation that combines lipids to form a membrane, which, in turn, can be used to compute parameters describing a membrane as a flexible sheet. Such parameters could be used for a simulation with many cells in order to obtain parameters that describe an organ, which could be used for a whole-body biological simulation. Each step, in theory, could be modeled in a different way using parameters derived not from experiment but from a more low-level form of simulation. This situation has not yet been realized, but it is representative of one trend in computational technique development. [Pg.276]

As an alternative, extremely sensitive detection can be achieved with reporter antibody probes tagged with intensely SERS-active compounds or with enzymes that react with substrates to yield SERS-active products. These methods often involve sandwich immunoassay techniques, which increase the number of required steps but offer the advantages of excellent sensitivity and the potential for label multiplexing. For example, Nie and coworkers recently reported the simultaneous detection of two types of antigens in a... [Pg.248]

While these methods both share the distinct advantage of looking directly at the active ingredient of the formulation they also share a number of disadvantages. Because of the small quantities released, sample preparation techniques, can frequently be elaborate and therefore very time consuming. Since each step in the preparation of a sample is a potential source of error, this increased complexity can also decrease the accuracy of the method. Considerations of this type led this laboratory to the use of labeled pheromones to decrease sample handling and to increase the quantitative accuracy, however, liquid scintillation counting does not provide qualitative information about the labeled species. [Pg.147]

At this moment, aminoacylation of tRNA with a nonnatural amino acid is still a bottleneck step for nonnatural mutagenesis both in vitro and in vivo. Hecht method is versatile to almost any types of amino acids, but can be done only for isolated tRNAs in a test tube. Further, the aminoacylation step of pdCpA is sometimes tricky. For aminoacylation in a test tube, micelle-mediated method is easier than the Hecht method, at least for some types of amino acids. The ribozyme technique of Suga is applicable to a variety of p-substituted phenylalanines and to a wide variety of tRNAs. This is, at present, the simplest and most dependable method of aminoacylation for isolated tRNAs. It has not been, however, applied to in vivo systems and to large-sized amino acids. Our PNA-assisted aminoacylation method may also be applicable to a wide variety of amino acids and tRNAs. Since the PNA-assisted aminoacylation is tRNA selective, it works as a potential amino acid donor in living cells. The orthogonal tRNA/aaRS pairs reported by Schultz and by Yokoyama are effective in some nonnatural amino acids with small side groups, but they have not been applied to large-sized amino acids, so far. [Pg.281]


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Method techniques

Potential Technique

Potential step

Potential step methods

Potential step techniques

Step methods

Stepping technique

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