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Beta band

Table I illustrates the utility of DRUV-visible data in determining the surface structures involving Ti. Samples of TS-1 were prepared by three different methods or treatments. Samples 1 and 2 were prepared by conventional hydrothermal synthesis and sample 3 by synthesis in a fluoride medium. TS-2 was synthesized as reported (7). At least five bands could be discerned by deconvolution (Fig. 3), at 205, 228, 258, 290, and 330 nm. Band 1 at 205 nm is assigned to tetrahedral, tetrapodal Ti present in TS-1, TS-2, and Ti-beta. Band 5 at 330 nm is assigned to an... Table I illustrates the utility of DRUV-visible data in determining the surface structures involving Ti. Samples of TS-1 were prepared by three different methods or treatments. Samples 1 and 2 were prepared by conventional hydrothermal synthesis and sample 3 by synthesis in a fluoride medium. TS-2 was synthesized as reported (7). At least five bands could be discerned by deconvolution (Fig. 3), at 205, 228, 258, 290, and 330 nm. Band 1 at 205 nm is assigned to tetrahedral, tetrapodal Ti present in TS-1, TS-2, and Ti-beta. Band 5 at 330 nm is assigned to an...
Published pharmaco-EEG trials provide a heterogeneous picture some studies with J-amphetamine and methylphenidate reported a reduction in delta and theta waves other authors found either an increase in delta and theta activity or no effect at all on the quantified EEG. There is also no agreement in the case of changes in the alpha and beta bands after several stimulants. Some of the contradictory findings are most likely to be due to different experimental conditions, particularly the duration of EEG recordings (for details see Spiegel, 1996, p. 90). [Pg.87]

Holthauzen, L. M., Correa, F., and Farah, C. S. (2004). Ca2+-induced rolling of tropomyosin in muscle thin filaments The alpha- and beta-band hypothesis revisited. J. Biol. Chem. 279, 15204-15213. [Pg.154]

They recorded EEG and local field potentials (LFPs) from macroelectrodes inserted into the subthalamic nucleus area in nine awake patients following functional neurosurgery for PD. Patients were studied after overnight withdrawal of medication. Coherence between EEG and SA LFPs was apparent in the theta (3-7 Hz), alpha (8-13 Hz), lower beta (14-20 Hz), and upper beta (21-32 Hz) bands, although activity in the alpha and upper beta bands dominated. Theta coherence predominantly involved mesial and lateral areas, alpha and lower beta coherence the mesial and ipsilateral motor areas, and upper beta coherence the midline cortex. SA LFPs led EEG in the theta band. In contrast, EEG led the depth LEP in the lower and upper beta bands. SA LFP activity in the alpha band could either lead or lag EEG. [Pg.254]

C. Familial dysbetalipoproteinemia (Type III pattern). A defect in the remnant particle apoprotein, which results in the loss of ability of remnants to bind to liver ceils. There are xanthomas and marked premature atherosclerosis. Remnant particles accumulate in the plasma, seen as a broad beta band on electrophoresis. There is elevation of both plasma cholesterol and triglycerides. [Pg.57]

Many cytochromes have been discovered since Kei-lin s first observation. Their nomenclature has developed empirically and has become most confusing. The important cytochromes can be grouped in three main families cytochrome a, cytochrome b, and cytochrome c. Each member of a family is characterized by specific absorption bands—alpha, beta, and gamma. The first occurs between 600 and 500 mp, the second around 500 and 525 mp, and the third in the neighborhood of 430 mp (Soret band). Upon oxidation, the alpha and beta bands become faint and only weak absorption is observed. During this oxidation process, the iron passes from the ferrous to the ferric form. [Pg.37]

Liver disease is a major cause of all kinds of abnormal lipoproteins. In lipoprotein electrophoresis it often causes a boring pattern no alpha-lipoproteins and a very broad beta-band. The latter is due to a host of abnormal or abnormally composed lipoproteins. In summary, we find decreased alpha-lipoproteins, a dissociation of A-I and A-II (a rare instance of the presence of LP-A-II) decreased LP-B, abnormal VLDL, poor in Apo-C, remnants in the LDL-class, and LP-X. [Pg.35]

Fig. 3.1 Curve 1 absolute intensity (except for an arbitrary constant) of the phosphorescent emission of crystal violet in glycerol at 178 K, showing the alpha and beta bands. Curve 2 similar absolute intensity of fluorescent emission (plus 5-10 % phosphorescence), at 178 K. Curve 3 for reference, the absorption spectrum. Curve 4 intensity of green phosphorescence band (not corrected for plate characteristics). Reprinted with permission from [3]. Copyright 1942, American Chemical Society... Fig. 3.1 Curve 1 absolute intensity (except for an arbitrary constant) of the phosphorescent emission of crystal violet in glycerol at 178 K, showing the alpha and beta bands. Curve 2 similar absolute intensity of fluorescent emission (plus 5-10 % phosphorescence), at 178 K. Curve 3 for reference, the absorption spectrum. Curve 4 intensity of green phosphorescence band (not corrected for plate characteristics). Reprinted with permission from [3]. Copyright 1942, American Chemical Society...
The most recent contribution to the separation of lipoproteins and to the study of lipoprotein patterns in various forms of hyperlipidemias is that of Fredrickson s (1966) group. Using a modified form of paper electrophoresis, Fredrickson and Lees (1966) described 5 different types of familial hyperlipoproteinemia, type II of which corresponds to EFH and is characterized by an intensely staining beta-band in their system. [Pg.423]

Engleman R Jr, Rouse P E, Peek H M and Biamonte V D 1970 Beta and gamma band systems of nitric oxide Los Aiamos Scientific Laboratory Report no LA-4364... [Pg.2087]

N9. Nishi, S Stoffel, M., Xiang, K Shows, T. B Bell, G. I., and Takeda, J Human pancreatic beta-cell glucokinase cDNA sequence and localization of the polymorphic gene to chromosome 7, band p 13. Diabetologia 35,743-747 (1992). [Pg.48]

The superhyperfine splittings are sufficiently small to ignore second-order effects at X-band, and for adducts of the nitrone compounds splitting from the nitrone-N and the beta-H are the only resolved hyperfine interactions, thus affording the extremely simple resonance condition (cf. Equation 5.10)... [Pg.170]

The discovery of Lp(a) by Berg in 1962 (B6) relied on the production of rabbit antisera against beta-lipoprotein and on the selective absorption of these antisera with individual human sera. When certain human sera were used for absorption, the antisera retained precipitation capacity in radial immunodiffusion with 30-35% of individual human sera, which obviously contained a previous unknown antigen. The particle carrying the new antigen shared antigenic properties with beta-lipoprotein, but had an additional antigenic structure. This was evidenced from the only partial fusion of the precipitin bands formed between a positive human serum, the antibeta lipoprotein antiserum and the new absorbed antiserum. [Pg.105]

Electrophysiological Tobacco smoking produces cortical activation on the EEG. Broadly, it reduces slow-wave activity (theta and delta) and increases activity in alpha and beta frequency bands (Knott et al. 1998 Pritchard et al. 1999). Other studies have found more isolated effects in alpha frequencies (Domino and Matsuoka 1994 Foulds et al. 1994). [Pg.112]

Infrared spectroscopy has been used to help solve or determine the structure of zeolites. The technique is particularly useful for identifying the presence of double four- and six-rings as well as five-membered pentasil rings. In the structural characterization of beta zeolite, Newsam and coworkers used a variety of techniques including IR, electron microscopy (TEM), X-ray diffraction (XRD) and sorption data to solve the stacked, faulted structure [57]. The presence of IR absorption bands at 1232 and 560cm indicated that the structure contained five-member pentasil building units. [Pg.115]

Spectrum 1 illustrates how the interaction with tetramethylbenzene (by hydrogen-bonding) shifts the silanol band in Beta to 3563 cm" and the bridging hydroxyls to even lower frequencies where overlapping absorption from hydrogen-bonded silanols make them difficult to detect In spectrum 1 the bands between 3100 and... [Pg.427]

Figure 13.20 IR spectra of tetramethylben- zeolite-only. Spectrum 13 tetramethylben-zene over H-form of Beta zeolite at 300°K and zene-only. The arrow points to the 1604cm 400°K. Spectrum 1 initial. Spectra 2-10 band assigned to the tetramethylbenzenium... Figure 13.20 IR spectra of tetramethylben- zeolite-only. Spectrum 13 tetramethylben-zene over H-form of Beta zeolite at 300°K and zene-only. The arrow points to the 1604cm 400°K. Spectrum 1 initial. Spectra 2-10 band assigned to the tetramethylbenzenium...
Fig. 6. Deconvolved amide F region FTIR spectra of apo- and heme-hemopexin. The amide F FTIR spectra of apo- and heme-hemopexin in D2 O were recorded and curve-fitted to resolve the individual bands. The differences between the original and fitted curves are shown in the upper traces in the panels. The estimated helix (15%), beta (54%), turn (19%), and coil (12%) content of the apo-protein are not significantly changed upon heme binding 104). This analysis was required because of the positive 231-nm elhpticity band in hemopexin and is consistent with the derived crystal structure results. Fig. 6. Deconvolved amide F region FTIR spectra of apo- and heme-hemopexin. The amide F FTIR spectra of apo- and heme-hemopexin in D2 O were recorded and curve-fitted to resolve the individual bands. The differences between the original and fitted curves are shown in the upper traces in the panels. The estimated helix (15%), beta (54%), turn (19%), and coil (12%) content of the apo-protein are not significantly changed upon heme binding 104). This analysis was required because of the positive 231-nm elhpticity band in hemopexin and is consistent with the derived crystal structure results.
A series of Beta zeolites have been synthesized in the presence of tetraethylammonium hydroxide (TEA). Samples with Si/Al ratio in the 7-100 range have been characterized by X-ray powder diffraction, I.R. spectroscopy, and pyridine adsorption. The fraction of TEA which is compensating the charge of the framework aluminum is removed at temperatures higher than those required to remove "occluded" TEA. Three hydroxyl bands are observed at 3740 cm l (silanol groups), 3680 cm" (extraframework Al) and 3615 cm 1 (acid hydroxyl groups interacting with pyridine). [Pg.49]

Figure 5. Intensity of the 3615 cm l band as a function of the aliaminum content of H-Beta zeolites. Figure 5. Intensity of the 3615 cm l band as a function of the aliaminum content of H-Beta zeolites.
Regarding EEG frequencies outside the delta band, several micro-architectural sleep EEG characteristics of depression have been sought in both the remitted and the symptomatic state [Armitage 1995]. Based on preliminary data, certain computerized sleep EEG patterns appear to be relatively specific to depression [e.g., an elevated fast frequency activity on the right hemisphere and a reduced beta and theta interhemispheric coherence] [Armitage et al. 1991, 1992c, 1993]. The consistency of all these findings, however, has not yet been established. [Pg.259]

The wavelengths of IR absorption bands are characteristic of specific types of chemical bonds. In the past infrared had little application in protein analysis due to instrumentation and interpretation limitations. The development of Fourier transform infrared spectroscopy (FUR) makes it possible to characterize proteins using IR techniques (Surewicz et al. 1993). Several IR absorption regions are important for protein analysis. The amide I groups in proteins have a vibration absorption frequency of 1630-1670 cm. Secondary structures of proteins such as alpha(a)-helix and beta(P)-sheet have amide absorptions of 1645-1660 cm-1 and 1665-1680 cm, respectively. Random coil has absorptions in the range of 1660-1670 cm These characterization criteria come from studies of model polypeptides with known secondary structures. Thus, FTIR is useful in conformational analysis of peptides and proteins (Arrondo et al. 1993). [Pg.149]


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