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Identical replication

The fabrication of assemblies of perfect nanometer-scale crystallites (quantum crystal) identically replicated in unlimited quantities in such a state that they can be manipulated and understood as pure macromolecular substances is an ultimate challenge in modem materials research with outstanding fundamental and potential technological consequences. [Pg.218]

Modem process facilities are computer controlled. Temperature and AT are programmed upward during the start of a growth cycle, pressure and temperature are monitored and controlled, and pressure and temperature overshoot alarms and overrides are provided. Such systems also store data from previous runs for correlations with properties or for identical replication of past conditions. [Pg.519]

No other physicochemical property has attracted as much interest in QSAR as the 1-octanol/watcr partition coefficient (log P). This is because of its direct relationship to membrane permeation and numerous other biological processes (also see Chapter 9). At first sight, the experimental measurement of log P seems to be a straightforward exercise. In practice, this is not the case because many factors affect the experimental determination of log P such as temperature, pH, and stability to degradation. As a result identical replicate samples can give very different log P values, and measurement by different... [Pg.655]

Coal A is an Appalachian (eastern U.S.) coal with 3.38% S and a specific surface of 23 cm /g (especially 0.5 to 5 mm sizes). Chemical analysis is the mean of samples from three identical replicate runs collected after 40 leaching days. The sample also has 50 mg/kg Be (Helz et al. 1987). [Pg.485]

PBC Periodic boundary conditions. The term periodic boundary conditions refers to the simulation of molecular systems in a periodic 3-D lattice of identical replicates of the molecular system under consideration. Using PBC allows to simulate the influence of bulk solvent in such a way as to minimize edge effects such as diffusion of a solute toward a surface or the evaporation of solvent molecules. [Pg.761]

A certain discrepancy between the values of k at the same temperature can be observed. This may be caused by the fact that the oxidation medium is not totally homogeneous, turning difficult the occurrence of an identical replication or by the difference in the oxygen amount dissolved in the medium. A difference in the linearity coefficient values was found 8.6556 for the first (straw) and 6.5263 for the second (bagasse), a 24.6% lower value (Figs. 3 and 4). These values are related to the concentration of the original lignin however, they are different probably by the same fact of the discrepancy between the k values. [Pg.660]

Lyne, A., Boston, R., Pettigrew, K., and 2 ech, L. (1992). EMSA A SAAM service for the estimation of population parameters based on model fits to identically replicated experiments. Comput. Methods Programs Biomed. 38,117-151. [Pg.278]

Figure 11.3 Results from Mo adsorption experiments. Solid symbols represent dissolved Mo and open symbols Mo adsorbed on synthetic birnessite (MnOx). Symbol shapes va with experimental temperature according to the legend. SSW denotes experiments run at an ionic strength of 0.7 M. The two bold error bars indicate the typical magnitude of comprehensive experimental uncertainty, based on a set of identical replicates. Reproduced from [20]. Figure 11.3 Results from Mo adsorption experiments. Solid symbols represent dissolved Mo and open symbols Mo adsorbed on synthetic birnessite (MnOx). Symbol shapes va with experimental temperature according to the legend. SSW denotes experiments run at an ionic strength of 0.7 M. The two bold error bars indicate the typical magnitude of comprehensive experimental uncertainty, based on a set of identical replicates. Reproduced from [20].
The ability of DNA for identical replication becomes plausible with the aid of Watson and Crick s structural model. Through the pairing of bases each individual strand determines a second and complementary strand. The mechanism of the biosynthesis of DNA follows the same concept. More will be said about this in the following section. [Pg.128]

Transformation and Transduction. Transformation factors of bacteria have produced important proof for the genetic role of DNA. Of some bacteria, e.g., the Pneumococci, different strains are known which produce different capsular material. The material (a polysaccharide cf. Chapt. XVII-7) must be regarded as one of the hereditary properties, just like hair coloration of mammals. It is possible to convert (to transform) bacteria of one type (e.g. type II) to another (e.g. type III) by treating them under certain conditions with an extract of tyjie III The active factor in the extract was prepared in pure form by Avery (1944) it is high molecular weight DNA. The assumption is that transformation is a transplantation of a gene. In the host bacterium, the transplanted nucleic acid, used in the process of transformation, acquires the capacity to induce characteristics—here the synthesis of type-specific capsular material. It also acquires in the host the capacity for identical replication, since the very same transformation factor can be isolated in quantity from a new harvest of transformed bacteria. [Pg.129]

The passing-on of genetic information requires, as we have seen, identical replication of DNA, which means de novo synthesis of deoxyribonucleic acid in strict conformity with an existing template. [Pg.129]

Calibration curves are usually constructed by analyzing a series of external standards and plotting the detector s signal as a function of their known concentrations. As long as the injection volume is identical for every standard and sample, calibration curves prepared in this fashion give both accurate and precise results. Unfortunately, even under the best of conditions, replicate injections may have volumes that differ by as much as 5% and often may be substantially worse. For this... [Pg.573]

Compared to bacterial cells, which are identical within a given cell type (except for O antigen variations), animal cells display a wondrous diversity of structure, constitution, and function. Although each animal cell contains, in its genetic material, the instructions to replicate the entire organism, each differentiated... [Pg.282]

DNA replication yields two DNA molecules identical to die original one, ensuring transmission of genetic information to daughter cells widi exceptional fidelity. [Pg.328]

FIGURE 11.21 Replication of DNA gives identical progeny molecules because base pairing is the mechanism determining the nucleotide sequence synthesized within each of the new strands during replication. [Pg.340]

FIGURE 12.1 DNA replication yields two daughter DNA duplexes identical to the parental DNA molecule. Each original strand of the double helix serves as a template, and the sequence of nucleotides in each of these strands is copied to form a new complementary strand by the enzyme DNA polymerase. By this process, biosynthesis yields two daughter DNA duplexes from the parental double helix. [Pg.357]

I Replication—the process by which identical copies of DNA are made so that information can be preserved and handed down to offspring I Transcription-—the process by which the genetic messages are read and carried out of the cell nucleus to ribosomes, where protein synthesis occurs... [Pg.1105]

The double helix model provides a simple explanation for cell division and reproduction. In the reproduction process, the two DNA chains unwind from each other. As this happens, a new matching chain of DNA is synthesized on each of the original ones, creating two double helices. Since the base pairs in each new double helix must match in the same way as in the original, the two new double helices must be identical to the original. Exact replication of genetic data is thereby accomplished, however complex that data may be. [Pg.628]

The characteristics of a covalent bond between two atoms are due mainly to the properties of the atoms themselves and vary only a little with the identities of the other atoms present in a molecule. Consequently, we can predict some characteristics of a bond with reasonable certainty once we know the identities of the two bonded atoms. For instance, the length of the bond and its strength are approximately the same regardless of the molecule in which it is found. Thus, to understand the properties of a large molecule, such as how DNA replicates in our cells and transmits genetic information, we can study the character of C=0 and N- H bonds in much simpler compounds, such as formaldehyde, H2C=0, and ammonia, NH,. [Pg.204]

Data. Several groups of n replicate measurements of a given property on each of m different samples (for a total of n = l (ni). The group sizes n,- need not be identical. [Pg.55]

It is revealing to look at an example of such data in Fig. 12. The UE56/2 beamline has two nominally identical branches with replicated optical paths, but that have been used for different experiments. The measurements show a high degree of circular polarization, [531 > 98%, except near carbon K edge where the polarization reduces, but only on one branch. It is postulated that this is a consequence of carbon contamination on a beamline optic in that branch. These results demonstrate the necessity to be alert to such possible causes of degradation and to perform polarization checks where possible rather than rely on theoretical predictions. [Pg.302]

In experiments with water-soluble inhibitors, the subsample was stirred under nitrogen during post-addition of an aqueous solution of the inhibitor followed by an aqueous sodium nitrite solution. Aliquots were weighed into 1-oz ointment jars, covered with nitrogen, sealed, and stored at 37 for later replicate analyses. Preparation of the positive control subsample was identical except that water was added in place of inhibitor. [Pg.151]


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See also in sourсe #XX -- [ Pg.127 , Pg.128 ]




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