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Labeling of reagent

In gas-phase reactions catalyzed by a solid surface, characterization of the chemisorbed species that are principally covering the surface can nowadays be made relatively easily by means of techniques such as IR and Raman spectroscopy, EELS, radioisotope labeling of reagents, and in some cases by nuclear magnetic resonance (NMR), electron spin resonance (ESR), and ESCA spectroscopies. In many cases, thermal desorption spectroscopy can be usefully applied to deduce indirectly the nature of species, and their distribution of energies of adsorption, that may have been strongly chemisorbed on the catalyst originally. [Pg.13]

Another part of input control is the proper labeling of reagents and materials. Proper identification should include the name, lot number (particular manufacturing batch), concentration, date received, date prepared, date opened, date of expiration, and recommended storage Conditions. In practice, such information is provided by manufacturers via a human-readable bar code. ... [Pg.497]

Examples of typical packaging labels from reagent grade chemicals. Label (a) provides the actual lot assay for the reagent as determined by the manufacturer. Note that potassium has been flagged with an asterisk ( ) because its assay exceeds the maximum limit established by the American Chemical Society (ACS). Label (b) does not provide assayed values, but indicates that the reagent meets the specifications of the ACS for the listed impurities. An assay for the reagent also is provided. [Pg.107]

In recent years, biochemists have developed an arsenal of reactions that are relatively specific to the side chains of particular amino acids. These reactions can be used to identify functional amino acids at the active sites of enzymes or to label proteins with appropriate reagents for further study. Cysteine residues in proteins, for example, react with one another to form disulfide species and also react with a number of reagents, including maleimides (typically A ethylmaleimide), as shown in Figure 4.11. Cysteines also react effectively... [Pg.95]

Various compounds of the type RAt, RAtCl2, R2AtCl and RAt02 (R = phenyl or p-tolyl) have been synthesized using astatine-labelled iodine reagents, e.g. ... [Pg.887]

A dual isotope labeling technique [85] has been used to measure membrane permeability in plant cells, based on the selective permeabiHty of the membranes of living cells to tritiated water and carbon-14 labeled mannitol. Kieran [29] showed that the results of the dual isotope labeling and Evan s Blue staining methods correlated well as indicators of cell viability however, the latter was preferable in terms of reagent cost and ease of analysis. [Pg.148]

After the addition of the non-radioactive material, the labeled material is added to the mixture and the mixture allowed to proceed toward equilibriim. In equilibrium analysis the order of addition of reagents is not critical as long as sufficient time is allowed for establishing equilibrium of the complete mixture (3,4). [Pg.59]

Preparation of Reagent and Labelling Procedures. The structure of F-D [2-(2,4-diazobicyclo-2,2,2-octyl)-4-(5-aminofluoresceinyl)-6-morpholinyl 1,3,5-triazine] has been confirmed by its FAB-MS, IR, and H-NMR spectra (9). Briefly, F-D was synthesized by the treatment of fluorescamine isomer I with cyanuric chloride, then reaction with morpholine and DABCO (l,4-diazobicyclo-2,2,2-octane), as illustrated... [Pg.63]

Maximum labelling of heparin with F-D was achieved at 5 hours at 25 °C, pH 8.4. In the case of heparin, the efficiency of labelling was not dependent on molecular weight, but solely a function of the ratio of the concentrations of labelling reagent to monosaccharide subunit in the reaction mixture. Similar results were encountered in the labelling of dextrans of different molecular weight (9). [Pg.70]

All such complexes can be thought of as potential. .irreversible labels of bio-molecules. A tris-chelate such as [Os(dipyridyl) 3]2+ will not behave as a reagent which has substitutional properties. Thus one limitation on the tjqpe of complex may well be that at least one or possibly two ligands should be monodentate as in [Pt(ethylenediamine)Cl2]. [Pg.14]


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See also in sourсe #XX -- [ Pg.274 ]




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Label reagents

Reagents labeled

Reagents labeling

Some examples of labeling with hydrophobic reagents

Use of Thiolation Reagents for Direct Labeling to Sulfhydryl Groups

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