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Quadrant analysis

However, single-point correlations are of limited value for two reasons. The first relates to the choice of the specific parameters to be correlated. Although there are some procedures in the literature that could be used for selecting the most appropriate parameter [e.g., the quadrant analysis (16,17)], these are not easy to apply in practice and the choice is usually based on a best-result basis. Another reason is that two processes having the same value of the chosen characteristic parameter can be different in terms of their overall shape. Consequently, a quantitative IVIVC is much more informative if established using all available in vitro and in vivo raw data these are termed multiple-point or point-to-point correlations. [Pg.233]

Analyze data from control antibody tube determine cutoff for quadrant analysis (Fig. 3A,B). [Pg.345]

Figure 1-5 Quadrant analysis of clinical predictivity. Reprinted from Regulatory Toxicology and Pharmacology, vol. 32/1, Olson et al., "Concordance of the Toxicity of Pharmaceuticals in Humans and in Animals 12, 2000, with permission from Elsevier. Figure 1-5 Quadrant analysis of clinical predictivity. Reprinted from Regulatory Toxicology and Pharmacology, vol. 32/1, Olson et al., "Concordance of the Toxicity of Pharmaceuticals in Humans and in Animals 12, 2000, with permission from Elsevier.
Fig. 19.24 Example of time-averaged correlation coefficient (left) and the quadrant analysis for a local correlation value (right)... Fig. 19.24 Example of time-averaged correlation coefficient (left) and the quadrant analysis for a local correlation value (right)...
The behavior of the different amines depends on at least four factors basicity, nucleophilicity, steric hindrance and solvation. In the literature (16), 126 aliphatic and aromatic amines have been classified by a statistical analysis of the data for the following parameters molar mass (mm), refractive index (nD), density (d), boiling point (bp), molar volume, and pKa. On such a premise, a Cartesian co-ordinate graph places the amines in four quadrants (16). In our preliminary tests, amines representative of each quadrant have been investigated, and chosen by consideration of their toxicity, commercial availability and price (Table 1). [Pg.103]

In the previous analysis for the second quadrant amines, there was evidence that the presence of an aromatic ring (BzAM) increased competition with the deactivating intermediate(s) and significantly the amount of DHQ obtained. The study was thus extended to other aromatic amines aniline (AN), 2-ethylaniline (2-ETAN), 3-ethylaniline (3-ETAN) and N-ethylaniline (N-ETAN). These amines are not classified in the literature analysis of amine properties (16), although aniline and pyridine were studied by statistical analysis of their solvent properties and classified in the same sector (16). By analogy, we hypothesize that these model aromatic amines should be classified in the second sector. Thus, they may aid in an understanding of the specific role of the aromatic ring and the effect of an alkyl substituent. [Pg.106]

X-ray and CD analysis. The structure of procyanidin B-1 was unequivocally confirmed by x-ray analysis of its deca-(9-acetyl derivative by Weinges, one of the pioneers in the field of proanthocyanidin chemistry. One of the most powerful methods to establish the absolute configuration at C-4 of the T-unit in dimeric A- and B-type proanthocyanidins remains the chiroptical method via application of the aromatic quadrant rule. This has been repeatedly demonstrated by the author s own work and several other contributions listed in Refs. 7-12. [Pg.574]

Fig. I. Analysis of lysed whole blood stained with FITC-anti-CD45 and PE-anti-CD14. (A) Scatter analysis, showing the position of a gate to restrict the analysis to lymphocytes. (B) Gated fluorescence analysis, showing that over 98% of the gated cells are in quadrant 4 (Q4). Monocytes would appear in quadrant 2 (Q2) and nonleukocytes in quadrant 3 (Q3). With suboptimal cell preparations, the position of the lymphocyte scatter gate can be determined by back-gating that is, examining the scatter distribution of cells gated by quadrant 4. Fig. I. Analysis of lysed whole blood stained with FITC-anti-CD45 and PE-anti-CD14. (A) Scatter analysis, showing the position of a gate to restrict the analysis to lymphocytes. (B) Gated fluorescence analysis, showing that over 98% of the gated cells are in quadrant 4 (Q4). Monocytes would appear in quadrant 2 (Q2) and nonleukocytes in quadrant 3 (Q3). With suboptimal cell preparations, the position of the lymphocyte scatter gate can be determined by back-gating that is, examining the scatter distribution of cells gated by quadrant 4.
With these patterns in mind, we conducted a principal components analysis of the two datasets using a covariance matrix, since some of the elements have especially high concentrations that could swamp those with lower concentrations in the analysis (Figure S). Here we can see that, in the plaza, samples from the north half vary by P concentration, while those of the south vary according to levels of Ba and Mg the reverse is true for western versus eastern samples (not pictured). In the patio, all samples tend to vary along Factor 1, in which Al, Ba, Fe, and Mn account for most of the variance in the data. This suggests that activity loci in the plaza and patio vary by comer or quadrant. [Pg.221]

Fig. 4.5. Quadrants are cursors or markers for delineating the intensity (according to channel number) of cells of interest in dual-parameter analysis. Fig. 4.5. Quadrants are cursors or markers for delineating the intensity (according to channel number) of cells of interest in dual-parameter analysis.
Fig. 8.26. The use of propidium iodide to exclude dead cells from analysis of a mouse spleen cell population for the expression of the Thy-1 surface antigen. The cells were stained with fluorescein for Thy-1 and then with propidium iodide to mark the dead cells. It can be seen that the dead cells (upper right quadrant) contribute to the fluorescein-positive population. Stained cells courtesy of Maxwell Holscher. Fig. 8.26. The use of propidium iodide to exclude dead cells from analysis of a mouse spleen cell population for the expression of the Thy-1 surface antigen. The cells were stained with fluorescein for Thy-1 and then with propidium iodide to mark the dead cells. It can be seen that the dead cells (upper right quadrant) contribute to the fluorescein-positive population. Stained cells courtesy of Maxwell Holscher.
Quadrant For dual-parameter analysis, a two-dimensional plot of particles according to the correlated fluorescence intensities of two colors is, traditionally, divided into four quadrants. The division is based on the background fluorescence of the unstained control sample. The quadrants, from this division, will contain (1) cells that have stained with the first fluorochrome only (2) cells that have stained with both fluorochromes (3) cells that remain unstained and (4) cells that have stained with the second fluorochrome only. In other words, the quadrants are defined so that they delineate the two types of single positive cells (1 and 4), double-negative cells (3), and double-positive cells (2). [Pg.253]

Fig. 2. Representative dot plots (PE anti-IL-4 vs. FITC anti-IFN-y) for the analysis of intracellular Th cytokines of CD4+ lymphocytes using the Fastlmmune Cytokine System (BD Pharmingen) by flow cytometry (a) a control subject and (b) an allergic asthmatic patient. The numbers in the quadrants denote the percentages of Thl and Th2 cells (W16). Reproduced with permission from C. K. Wong, C. Y. Ho, F. W. S. Ko, C. H. S. Chan, A. S. S. Ho, D. S. C. Hui, and C. W. K. Lam. Proinflammatory cytokines (IL-17, IL-6, IL-18 and IL-12) and Th cytokines (IFN-y, IL-4, IL-10 and IL-13) in patients with allergic asthma. Clin. Exp. Immunol. 125 177-183, Copyright Blackwell Science Ltd., 2001. Fig. 2. Representative dot plots (PE anti-IL-4 vs. FITC anti-IFN-y) for the analysis of intracellular Th cytokines of CD4+ lymphocytes using the Fastlmmune Cytokine System (BD Pharmingen) by flow cytometry (a) a control subject and (b) an allergic asthmatic patient. The numbers in the quadrants denote the percentages of Thl and Th2 cells (W16). Reproduced with permission from C. K. Wong, C. Y. Ho, F. W. S. Ko, C. H. S. Chan, A. S. S. Ho, D. S. C. Hui, and C. W. K. Lam. Proinflammatory cytokines (IL-17, IL-6, IL-18 and IL-12) and Th cytokines (IFN-y, IL-4, IL-10 and IL-13) in patients with allergic asthma. Clin. Exp. Immunol. 125 177-183, Copyright Blackwell Science Ltd., 2001.
The first reactor in the 3-CSTR process has a conversion rate of 72.8%, and the reactant concentration in this first reactor is 2.18 kmol/m3. The reactor volume is low (14.3 m3), and the jacket heat transfer area is only 24.5 m2. The resulting jacket temperature (300 K) is almost down to the inlet cooling water temperature of 294 K. Linear analysis gives a Nyquist plot that never drops into the third quadrant, so the critical (—1,0) point cannot be encircled in a counterclockwise direction. This is required for closedloop stability because the openloop system is unstable and has a positive pole. Thus a proportional controller cannot stabilize this first reactor. [Pg.131]

In making an analysis of a small crystal we place it at the center of an X-ray spectrometer, provided with an ionization chamber and a quadrant electrometer. The slits of the instrument should be fairly narrow, and... [Pg.6]

SWOT is the business analysis technique used most commonly by companies and other organisations. SWOT stand for Strengths, Weaknesses, Opportunities and Threats. It is usually set out in quadrants on a single sheet of paper as illustrated in Figure C4. The contents of the SWOT analysis are usually generated by a brainstorming technique (see Section C, 1.8.3). [Pg.164]

A similar analysis may be carried out for the electron detachment poles as well and the Auger poles (Eq — E 1( )) will obviously be found in the first quadrant of the complex E-plane. With this brief discussion of the pole structure of the complex scaled electron propagator as a common background, its utility in direct and simultaneous treatment of resonances of N+l electron and N-l electron systems becomes manifest e.g., for Be both Be+ (Is-1) 2S Auger and 2P Be- shape resonances have been calculated simultaneously from a single calculation on Be/25,26/. [Pg.240]


See other pages where Quadrant analysis is mentioned: [Pg.18]    [Pg.324]    [Pg.628]    [Pg.183]    [Pg.101]    [Pg.787]    [Pg.25]    [Pg.18]    [Pg.324]    [Pg.628]    [Pg.183]    [Pg.101]    [Pg.787]    [Pg.25]    [Pg.130]    [Pg.116]    [Pg.73]    [Pg.94]    [Pg.1083]    [Pg.1092]    [Pg.343]    [Pg.82]    [Pg.29]    [Pg.342]    [Pg.343]    [Pg.162]    [Pg.72]    [Pg.52]    [Pg.105]    [Pg.19]    [Pg.28]    [Pg.302]    [Pg.244]    [Pg.151]    [Pg.146]    [Pg.72]   
See also in sourсe #XX -- [ Pg.324 ]

See also in sourсe #XX -- [ Pg.183 , Pg.201 ]




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Quadrantes

Quadrants

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