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Of markers

The major problem in such conversions is the degradation of the branched carbon side-chain on C-17 which is present in all abundant steroids and lacking in all steroid hormones. The most important starting material used in industry today is diosgenin from the Mexican dioscorea plant. It is degraded by the method of Marker to 16-dehydropregnenolone in 45% total yield. This compound is a key substance in the production of several hormones with anabolic, catabolic, and sexual effects. [Pg.283]

Oxide movements are determined by the positioning of inert markers on the surface of the oxideAt various intervals of time their position can be observed relative to, say, the centreline of the metal as seen in metal-lographic cross-section. In the case of cation diffusion the metal-interface-marker distance remains constant and the marker moves towards the centreline when the anion diffuses, the marker moves away from both the metal-oxide interface and the centreline of the metal. In the more usual observation the position of the marker is determined relative to the oxide/ gas interface. It can be appreciated from Fig. 1.81 that when anions diffuse the marker remains on the surface, but when cations move the marker translates at a rate equivalent to the total amount of new oxide formed. Bruckman recently has re-emphasised the care that is necessary in the interpretation of marker movements in the oxidation of lower to higher oxides. [Pg.271]

We cannot progress any further at this point without assuming something about the distribution of markers. It is this distribution that effectively determines the... [Pg.461]

Rutherford backscattering (RBS) He 4He 30 nm heavy atoms jim — movement of markers... [Pg.363]

Harrison et al., 1998 10 week old OVX rats low calcium diet treatment starts 2 weeks after OVX Soy protein with isoflavones (6 mg/d) for 4 weeks Reduced bone loss (higher bone weight, higher calcium content) but no decrease of markers of bone turnover for the soy group... [Pg.94]

Caramel color interacts with other food components. As an example, a concentration higher than 700 ppm caramel in cola increased the rate of hydrolysis of the aspartame, forming alpha-L-aspartyl-L-phenylalanine. Caramelization products inhibited enzymic browning by 85.8 and 72.2% when heated at pH 4 and 6, respectively, for 90 min. The highest inhibitory activity was found for the fraction with molecular weight of 1000 to 3000. Caramel is often used for adulteration of juices and other foods like honey or coffee. It can be determined by quantification of marker molecules such as 5-HMF, 4-Mel, and DFAs. ... [Pg.340]

Hours after inoculation of self-induced anaerobic culture. Organelle identified by peak of marker enzyme activity. [Pg.865]

It is appropriate at this stage to evaluate procedures that will be used to assess the effectiveness of bioremediation, which have been discussed in Chapter 13. These may include (a) use of radiolabeled substrates (although these will not generally be permitted in field operations) and the application of C-labeled substrates, (b) evaluation of the occurrence of metabolites, and (c) evaluation of markers such as specific enzymes. [Pg.691]

Immunoassays have been based on the potentiometric measurement of marker ions such tetrapentylammonium ion (TPA ) that are loaded in phospholipid liposomes Complement mediated immunolysis of these loaded vesicles is caused... [Pg.16]

The researeh on dehydroepiandrosterone (DHEA) is limited beeause of the laek of radiolabeled metabolites. Robinzon et al. [126] showed that, using pig liver mierosomes, the radiolabeled metabolites of DHEA can be prepared in stable, pure form for bioehemical smdies. They utilized pig liver microsomal (PLM) fractions to prepare pH]-labeled 7a-hydroxy-DHEA (7a-OH-DHEA), 7[3-hydroxy-DHEA (7P-OH-DHEA), and 7-oxo-DHEA substrates from 50 pM [1,2,6,7-3H]DHEA. The metabolites were separated by silica gel PLC plates using ethyl aeetate-hexane-gla-eial aeetic acid (18 8 , v/v) as the mobile phase, extracted with ethyl aeetate, and dried under a stream of nitrogen. The purity of markers was determined with the use of TLC and GC/MS. [Pg.231]

A method should be able both to quantify the amount of marker drug residue present in the sample and to identify the compound unambiguously. Historically, this required two distinct procedures a determinative procedure used to quantify the analyte, and a confirmatory procedure used to unequivocally identify the analyte. The need for two procedures was driven by the limitations of available technology. Most determinative methods over the last two decades have been based on liquid chromatography, usually with ultraviolet (UV)/visible or fluorescence defection. Limitations of cost. [Pg.79]

An official document containing prerequisites for the use of marker compounds does not exist. However, in the author s experience the following rules may be used as guidance ... [Pg.98]

Torres, A. R., Krueger, G. G., and Peterson, E. A., Purification of Gc-2 globulin from human serum by displacement chromatography a model for the isolation of marker proteins identified by two dimensional electrophoresis, Anal. Biochem., 144, 469, 1985. [Pg.127]

Number of markers and 14-d risk of death, myocardial infarction, or urgent revascularization... [Pg.22]

Kinter AL, Umscheid CA, Arthos J, et al. HIV envelope induces virus expression from resting CD4+ T cells isolated from HIV-infected individuals in the absence of markers of cellular activation or apoptosis. J Immunol 2003 170(5) 2449-2455. [Pg.286]

Y Sela, S Magdassi, N Garti. Release of markers from the inner water phase of W/O/W emulsions stabilized by silicone based polymeric surfactants. J Control Release 33(1) 1-12, 1995. [Pg.286]

Fig. 16 Contours of fluorescent intensity in frozen sections of the rabbit eye following 15 pL injection of marker solution in the central vitreous cavity injection was conducted through the superior rectus muscle 15 hours following injection of 0.2% sodium fluorescein 14 days following injection of 0.1% FITC-dextran, molecular weight 66,000. (From Ref. 230.)... [Pg.448]

E. R Segregation of marker loci in families with an inherited paracentric insertion of chromosome 9. Am. J. Hum. Genet. 39, 612-617 (1986). [Pg.37]

Release of markers bound to the endothelial cell such as thrombomodulin is indicative of vascular damage. Increased levels of soluble thrombomodulin in plasma are diagnostic (93). Other endothelium-derived markers such as 6-keto-prostaglandin F a, which is a metabolite of prostacyclin, are useful in the assessment of endothelial function, with lower levels indicative of inability to synthesize this marker due to defective or damaged endothelium through plaque formation (93). [Pg.155]

These decision levels calculated on the basis of marker levels found in patients with confirmed advanced malignancies should indicate a very high probability of the presence of malignancy. [Pg.187]

Fry, PM, DL Hudson, MH O Hare, and JRW Masters. 2000. Comparison of marker protein expression in benign prostatic hyperplasia in vivo and in vitro. BJU Int 85 504—513. [Pg.460]

Tab. 5.1. List of marker compounds used to establish relationship between oral dose absorbed in humans (Fa) and apparent permeability coefficient in Caco-2 monolayers. Tab. 5.1. List of marker compounds used to establish relationship between oral dose absorbed in humans (Fa) and apparent permeability coefficient in Caco-2 monolayers.

See other pages where Of markers is mentioned: [Pg.243]    [Pg.244]    [Pg.2039]    [Pg.17]    [Pg.98]    [Pg.462]    [Pg.278]    [Pg.147]    [Pg.354]    [Pg.355]    [Pg.355]    [Pg.13]    [Pg.28]    [Pg.16]    [Pg.69]    [Pg.87]    [Pg.98]    [Pg.307]    [Pg.324]    [Pg.158]    [Pg.156]    [Pg.184]    [Pg.237]    [Pg.158]    [Pg.511]    [Pg.39]    [Pg.41]    [Pg.41]    [Pg.41]   
See also in sourсe #XX -- [ Pg.194 ]




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Aspects and Applications of Tumor Markers

Biochemical markers of bone mineral

Biochemical markers of bone mineral density

Biochemical markers of bone turnover

Biological Markers and Early Diagnosis of AD

Chemical markers of sterility

Chromatography of food irradiation markers

Classes of Markers

Determination of a Marker Enzyme Ouabain-Sensitive Na,K-ATPase

Determination of marker substances by high-pressure liquid chromatography

Development of Multi-marker-based Diagnostic Assays with the ProteinChip System

Direct detection of redox markers

Estimation of Markers Distributions Near the Virtual K-Plane

Identification of Protein Markers

Light Scattering and Emission Markers for Analysis of Blood

Marker for detection of changes during

Marker for detection of changes during heat processing and storage

Markers of DNA Oxidative Damage

Markers of bone turnover

Markers of oxidative stress

Molecular markers of cancer

Novel markers at the proteome level glycosylation of proteins

Polarized Luminescence of Macromolecules with Conjugated Luminescent Markers

Production Strains Devoid of Antibiotic Resistance Markers

Quantitative evaluation of Elbe river derived organic marker compounds in sediment samples from the German Bight

Spatial Distribution of Markers

Surrogate Markers in Different Stages of Drug Development Processes

Targeting tumour vessels using markers of angiogenesis

The use of molecular markers in organic breeding programs

Turning SNPs into Useful Markers of Drug Response

Types of Markers

Wrapping as a Marker of Local De-wetting Propensity

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