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Isolation and analysis

The real advantage of frequency-domain analysis is the ability to normalize each vibration component so that a complex machine-train spectrum can be divided into discrete components. This ability simplifies isolation and analysis of mechanical degradation within the machine-train. [Pg.686]

Fig. 5. Methods used for isolation and analysis of genes for which a product... Fig. 5. Methods used for isolation and analysis of genes for which a product...
Several studies characterizing the reactions of alkenyl radicals with quinone dumines and quino-neimines were published in the late 1970s. Quinone dumines react with allylic radicals yielding both the reduced PPD and the alkylated product. In these experiments 2-methyl-2-pentene served as a model olefin (model for NR). Samples of the olefin and quinoneimines or quinone diimine were heated to 140°C. Isolation and analysis of products demonstrated that 40%-70% of the imine or diimine was reduced to the corresponding PPD, while 20%-50% was isolated as the alkylated product. This alkylation reaction (via an allylic radical) represents the pathway to the formation of rubber-bound antidegradant. ... [Pg.489]

Schiedt, K. and Liaaen-Jensen, S., Isolation and analysis, in Carotenoids Isolation and Analysis, lA, Britton, G., Liaaen-Jensen, S., and Pfander, H., Eds., Birkhauser, Basel, 1995, 81. [Pg.473]

Isolation and Analysis of Multiple Tomato psubunit Genomic Clones and Related cDNAs from Arabidopsis. [Pg.259]

Weedon, B. C. L. and G. P. Moss (1995). Structure and nomenclature. Carotenoids, Isolation and Analysis. G. Britton, S. Liaaen-Jensen and H. Pfander, eds. Basel, Switzerland Birkauser Verlag, pp. 1A. [Pg.227]

Poly(3HAMCL)s have also been produced from free fatty acid mixtures derived from industrial by-products which are potentially interesting low-cost renewable resources. Isolation and analysis of the polymer allowed the identification of 16 different saturated, mono-unsaturated and di-unsaturated monomers [46]. Except for the presence of diene-containing monomers and a large number of minor components, the composition of the fatty acid mixture derived PHA did not differ significantly from oleic acid derived PHAs. [Pg.168]

A significant advantage of this method is that is provides quantitative information since the IEF technique actually separates the phospho- and dephospho- forms of the protein, the ratio of these species as detected by IEF/immunoblotting is a direct readout of the protein s phosphorylation status within the cell (assuming no selective loss of one species during isolation and analysis). [Pg.164]

Lemke, G., Lamar, E. and Patterson, J. Isolation and analysis of the gene encoding peripheral myelin-protein zero. Neuron 1 73-83,1988. [Pg.120]

Graham J, Higgins JA. Biomembrane Protocols. I. Isolation and Analysis, Humana Press, Totowa, NJ, 1993. [Pg.192]

Table 4 Current methods for the isolation and analysis of toxic compounds found in papermill waters... [Pg.35]

L. van Heukelem and C.S. Thomas, Computer assisted high-performance liquid chromatography method development with applications to the isolation and analysis of phytoplankton pigments. J. Chromatogr.A 910 (2001) 31—49. [Pg.363]

Liu S, Sjovall J, Griffiths WJ. 2003. Neurosteroids in rat brain extraction, isolation, and analysis by nanoscale liquid chromatography-electrospray mass spectrometry. Anal Chem 75 5835. [Pg.172]

On the other hand, some compounds which are Included may not be true Gossypium secondary metabolites. Not only are the sources mentioned above possible contributors of exogenous compounds which have been Included in the accompanying Tables (I - X), but also it is quite possible that methods of isolation and analysis caused molecular transformation which created Isomers of true metabolites or even caused more drastic alterations. The diversity of structures which are plausible natural products is so great that it is not reasonable to exclude many of those reported simply on the basis of structure assignment. For this reason, it can be expected that some errors of inclusion have been made. [Pg.277]

Larran S et al.. Isolation and analysis of endophytic microorganisms in wheat Triticum aestivum L.) leaves, WorldJMicrobiol Biotechnol 18 683—686, 2002. [Pg.565]

IJ Cartwright. Separation and analysis of phospholipids by thin layer chromatography. In JM Graham, JA Higgins, eds. Methods in Molecular Biology. Vol. 19 Biomembrane Protocols I. Isolation and Analysis. Totowa, NJ Humana Press, 1993, pp 153-167. [Pg.185]

Graham JM (1993) The identification of subcellular fractions from mammalian cells. In Graham J, Higgins J (eds.) Meth Molec Biol, vol. 19. Biomembrane protocols. 1. Isolation and analysis. Humana Press, To-towa, N.J., p 1... [Pg.171]

Yates, S. G., and R. E. England. Isolation and analysis of carrot constituents myristicin, falcarinol, and falcarindiol. J Agr Food Chem 1982 30(2) 317-320. [Pg.218]

A review of the literature shows that alkaline conditions have often been used in the isolation and analysis of nitrosamines in food stuffs and in other natural samples (19,20). We considered it possible that these conditions which involve digestion of the sample with alcoholic hydroxides could produce fragmentation... [Pg.119]

Exact analysis of sialic acid is required in biologieal experiments where the biological role of sialic acid is frequently studied with the aid of sialidases, and the amount of sialic acids released is determined. This is also important for periodate oxidation studies on biological systems, where modification of sialic acids by periodate is only assumed, but chemical analysis of this effect by isolation and analysis of the modified sialic acids is seldom performed. These uncertainties in determinations of sialic acid can be overcome by the purification procedures already described. Furthermore, it must be stressed that unequivocal determination of the structure of a sialic acid, especially... [Pg.152]

Tretyakova, N., Sangaiah, R., Yen. T.Y, Gold, A. Swenberg, J.A. (1997b) Adenine adducts with diepoxy butane isolation and analysis in exposed calf thymus DNA. Chem. Res. Toxicol., 10, 1171-1179... [Pg.222]

Early studies using resins for isolation and analysis of trace organics, such as pesticides, PCBs, and organic acids, from small volumes of water showed excellent recovery and the potential of easy application to environmental samples. Isotherm studies in distilled water were used to define the sampling parameters for quantitative analysis of these compounds. Later, studies using resin samplers for large-volume environmental samples were extrapolated from the early low-volume resin work of Junk et al. (5,14) and Thurman et al. (27) (see Table I). [Pg.271]

Clearly, branched arabinans are important, primary cell-wall components, but considerable further study is needed before it will be possible to draw even a tentative structure for the intact-wall component. Isolation and analysis of the arabinan of sycamore cell-wall is of current interest, a study augmented by the availability of two purified enzymes, endo-a-(l— 5)-arabinanase63 133 and exo-a-arabinosidase.63... [Pg.282]

Experiment 14 introduced students to some principles and techniques involved in recombinant DNA research. Specifically, the experiment outlined the replication, isolation, and analysis of bacterial plasmid vehicles for molecular cloning experiments. This experiment describes another tool that is essential in hybrid plasmid construction and analysis-restriction enzyme action. The procedures introduced here have also found widespread use in the analysis and characterization of all DNA molecules. [Pg.431]

Table I (104) shows the yields of products from maltose to malto-pentaose recovered from digests of 0.2 M crystalline a-D-glucosyl fluoride with crystalline a-amylase preparations from six different biological sources. The digests were incubated at 30 °C for 10 minutes, heat inactivated, and chromatographed for product isolation and analysis. Table I (104) shows the yields of products from maltose to malto-pentaose recovered from digests of 0.2 M crystalline a-D-glucosyl fluoride with crystalline a-amylase preparations from six different biological sources. The digests were incubated at 30 °C for 10 minutes, heat inactivated, and chromatographed for product isolation and analysis.

See other pages where Isolation and analysis is mentioned: [Pg.33]    [Pg.104]    [Pg.141]    [Pg.476]    [Pg.638]    [Pg.656]    [Pg.298]    [Pg.105]    [Pg.54]    [Pg.78]    [Pg.31]    [Pg.450]    [Pg.503]    [Pg.163]    [Pg.50]    [Pg.603]    [Pg.9]    [Pg.408]    [Pg.766]    [Pg.408]   


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Analysis of ADP-Ribosylation Patterns in Isolated Nuclei and Nucleosomal Fragments

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