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Serum charged with human

Figure 3. The inhibition of E. coli around wells charged with human serum or Tr and the neutralization of microbiostasis on serum medium around wells charged with a solution of ferric ammonium citrate (20 i g iron/well) or spent medium at 15-, 25-, and 35-hr incubation period (25)... Figure 3. The inhibition of E. coli around wells charged with human serum or Tr and the neutralization of microbiostasis on serum medium around wells charged with a solution of ferric ammonium citrate (20 i g iron/well) or spent medium at 15-, 25-, and 35-hr incubation period (25)...
Recently Tanford and his collaborators have made use of the electrostatic term w to analyze the titration curves of a number of proteins. By combining graphical methods and trial-and-error selection they obtained values of p(Kint) and w from experimental titration curves. In each case the value for the apparent average net charge was corrected for the binding of anions and cations as determined by independent experimental methods. Differences between their experimental values of w and those calculated from theory were interpreted by these workers in terms of alterations in molecular parameters or structure. For example, observed values which were low, especially when they became low only at pH s far removed from neutrality, were attributed to alteration in the size or shape of the molecule brought about by electrostatic repulsion. Thus, with human serum albumin Tanford (1950) found that although the basic branch of the titration curve could be computed from theory, the acid branch was much too steep... [Pg.159]

ICP-AES was validated for the simultaneous determination of Al, B, Ba, Be, Cd, Co, Cr, Cu, Fe, Li, Mn, Ni, Pb, Se, Sr and Zn in human serum in a clinical laboratory. The samples underwent digestion and yttrium was used as an internal standard. The LOD were as follows 0.002-0.003 (xM for Ba, Cd, Mn and Sr 0.014-0.07 (xM for Be, Co, Cr, Cu, Fe, Li, Ni, Pb and Zn and 0.2-0.9 (xM for Al, B and Se. The concentrations of Al, Be and Co in human serum were found to be above the LOD, while those of Cd, Cr, Ni and Pb were below the LOQ however, in case of acute intoxication with the latter elements the method is valid . Matrix effects were evaluated for ICP-AES analysis using solution nebulization and laser ablation (LA) techniques. The main matrix-related interferences stem from elements with a low second ionization potential however, these are drastically reduced when pure He is used as carrier gas. This points to Ar (the usual carrier) participation in the interference mechanism, probably by interacting with doubly charged species. ... [Pg.325]

Figure F2.4.1 Liquid chromatography/mass spectrometry (LC/MS) analysis of isomeric carotenes in a hexane extract from 0.5 ml human serum. Positive ion electrospray ionization MS was used on a quadrupole mass spectrometer with selected ion monitoring to record the molecular ions of lycopene, p-carotene, and a-carotene at m/z (mass-to-charge ratio) 536. A C30 HPLC column was used for separation with a gradient from methanol to methyl-ferf-butyl ether. The a -trans isomer of lycopene was detected at a retention time of 38.1 min and various c/ s isomers of lycopene eluted between 27 and 39 min. The all-frans isomers of a-carotene and P-carotene were detected at 17.3 and 19.3 min, respectively. Figure F2.4.1 Liquid chromatography/mass spectrometry (LC/MS) analysis of isomeric carotenes in a hexane extract from 0.5 ml human serum. Positive ion electrospray ionization MS was used on a quadrupole mass spectrometer with selected ion monitoring to record the molecular ions of lycopene, p-carotene, and a-carotene at m/z (mass-to-charge ratio) 536. A C30 HPLC column was used for separation with a gradient from methanol to methyl-ferf-butyl ether. The a -trans isomer of lycopene was detected at a retention time of 38.1 min and various c/ s isomers of lycopene eluted between 27 and 39 min. The all-frans isomers of a-carotene and P-carotene were detected at 17.3 and 19.3 min, respectively.
AQ/Qo = (Q - Qo)/Qo, where Q0 is charge consumption without analyte and Q is that at certain thrombin, concentration. An example of calibration curve for two independently prepared electrodes is shown in Fig. 47.3. It is seen, that results are well reproducible. Statistical analysis, performed earlier [4] revealed that standard error is approximately 11%. Interferences of this aptasensor with other compounds, human serum albumine (HSA) and human IgG are relatively low. An example is shown in Fig. 47.4, where calibration curve for thrombin is compared with those for HSA and IgG. Please note, that concentrations of HSA and IgG are much higher in comparison with that of thrombin. [Pg.1274]

In addition to substantial differences in the sorption behavior of products, the moisture distribution in each vial of one charge must be considered when the SD process is developed. Pikal and Shaw [1.59] studied this distribution in dextran 40, human serum albumin (HSA), bovin somatotropin (BST) and glycine. Thirty vials where filled with 10 or 20 mm cake thickness, loaded on shelves at 5 °C, cooled to -40 °C and frozen in 30-45 min. Tc was determined for all products as >-12 °C. In Table 1.10.6 the water content of four products is shown in four different positions... [Pg.98]


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