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Surfaces of Organisms

Figure 3.3 Cell surface display. Proteins displayed on the cell surface of organisms bind a fluorescent molecule. Cells are passed through a FACS machine, allowing separation into populations that do or do not bind the target... Figure 3.3 Cell surface display. Proteins displayed on the cell surface of organisms bind a fluorescent molecule. Cells are passed through a FACS machine, allowing separation into populations that do or do not bind the target...
Fortunately, ground waters dissolve and transport metals from mineral deposits at depth to the surface, where the metals adsorb onto the surfaces of organic matter and Fe- and Mn-oxy-hydroxide particles in the soil. Unfortunately, the adsorption of these ions contributes only a small amount of additional metal to the soil, resulting in marginally anomalous... [Pg.23]

Podzorov V, Menard E, Borissov A, Kiryukhin V, Rogers JA, Gershenson ME (2004) Intrinsic charge transport on the surface of organic semiconductors. Phys Rev Lett 93 086602... [Pg.64]

Several evidences, reported in the literature and briefly reviewed in the present article, demonstrate that the carbohydrate recognition at the surface of organized systems is somewhat different from that observed in isotropic media. These differences lie in (1) the conformation of carbohydrate which is affected by hydrophobization and by the nature of the surrounding lipids, (2) cluster effects from which can result in high energies of binding and which are affected by the fluidity of the lipid system, (3) entropy changes at the surface of a supra-molecular structure. [Pg.307]

Daubendiek et al.55 have extended this technique to demonstrate electronic energy transfer at the gas-solid interface. They irradiated photosensitizers, in polycrystalline form, in the presence of m-piperylene vapor and found that the extent of isomerization was comparable to values obtained for the same sensitizer in a solution of piperylene. Their results indicated an energy difference of about 1 kcal between triplet states of sensitizers in solution and on the surface of organic crystals. [Pg.331]

Before describing dye sensitized electron transfer reactions at the surface of organic crystals a few remarks shall be made concerning experimental peculiarities of the system. [Pg.59]

The interaction leading to the adsorption of rhodamine at the surface of organic crystals and also the dye coverage 6 can be deduced from properties of... [Pg.69]

To obtain a better control over the number of dye molecules at the crystal surface, sensitized current measurements have been carried out with dye molecules incorporated into a fatty acid layer deposited at the surface of an organic crystal and in contact with an eletrolytic solution at the other side 102>. However, the experimental technique which alllows for the reproduction of known experimental results for fatty acid layers deposited on glass slides and on aluminium-oxide 103,104) (joes not yield a satisfactory preparation of such layers at the hydrophobic surface of organic crystals 105>. [Pg.73]

Fig. 31. Quantum yield (filled circles) of rhodamine sensitized hole generation at the surface of organic crystals relative to perylene W/Wpe versus the ionisation energies 7C of the organic crystals (lower abcissa). The range of the estimate for the value at phenanthrene is indicated by the wiggled arrow. The activation times for electron transfer and back electron transfer Tjg are also shown (compare Section IV 7)... Fig. 31. Quantum yield (filled circles) of rhodamine sensitized hole generation at the surface of organic crystals relative to perylene W/Wpe versus the ionisation energies 7C of the organic crystals (lower abcissa). The range of the estimate for the value at phenanthrene is indicated by the wiggled arrow. The activation times for electron transfer and back electron transfer Tjg are also shown (compare Section IV 7)...
Endowing these polymolecular entities with recognition units and reactive functional groups may lead to systems performing molecular recognition or supramolecular catalysis on external or internal surfaces of organic (molecular layers, membranes, vesicles, polymers, etc.) [7.1-7.13, A.41] or inorganic (zeolites, clays, sol-gel preparations, etc.) [7.14-7.20] materials. [Pg.81]

The results demonstrate that the surfaces of organic expls, ie, RDX and HMX, are of relative-... [Pg.131]

SIMS has become a diverse tool in the study of many different substances other than metals and semiconductors. This part of the paper discusses the secondary ion emission of molecular and polyatomic ions from the surfaces of organic compounds including polymers and biomolecules. [Pg.173]

Epithelium Form a protective layer, allow secretion/excretion Linings and surfaces of organs... [Pg.36]

Surface protection A thin protective metal oxide layer can be formed on the surface of organic or inorganic substrates Priming of the substrate by solutions of titanium/zirconate or by partial hydrolyzing and heating or chemical vapor deposition... [Pg.192]

Stability of both foam and asymmetric aqueous films at the surface of organic liquids of different polarity has been studied as function of the surfactant concentration [551], Microscopic foam films were obtained in a glass cuvette (Tig. 3.120,c) by blowing an air bubble at the tip of a vertical capillary immersed into the surfactant solution. With a micrometric screw (not shown in the figure) the bubble was pressed carefully onto the solution/air interface, thus forming the film. [Pg.320]

Surfactant concentration ensuring formation of stable aqueous films at the surface of organic liquids... [Pg.321]

Similar results have been obtained in the study of foam breakdown by alcohols using a special device for determination of the rate of contact foam breakdown [69]. The foam was supplied at constant rate over the surface of organic solvent. The rate of foam breakdown was determined in two regimes impulse and continuous. In the impulse regime, after contacting the organic solvent, the foam expanded as a consequence of its breakdown in the contact zone and detached itself from the solvent surface. Since the foam was constantly supplied, after a... [Pg.647]

Surfaces of organisms have strong affinity for heavy metals such as Cu(II), Pb(II), Zn(II), Cd(II), and Ni(II) (surface complex formation). [Pg.659]

The data shown below, in Fig. 4.4, illustrate the richness of local information that can be extracted. On a micropattemed surface of organic molecules exposing hydrophobic -CH3 and hydrophilic -COOH groups at the film surface (prepared by microcontact printing [23]), the border region of the printed pattern was investigated in AFM-FV measurements. F-d curves were acquired pixel-per-pixel and provided information of local tip-surface interactions as shown in panels a and b. Here, the difference in pull-off force between the two chemically distinct regions and the tip is clearly pronounced. [Pg.193]


See other pages where Surfaces of Organisms is mentioned: [Pg.1703]    [Pg.237]    [Pg.108]    [Pg.7]    [Pg.693]    [Pg.622]    [Pg.384]    [Pg.277]    [Pg.307]    [Pg.510]    [Pg.71]    [Pg.72]    [Pg.80]    [Pg.307]    [Pg.1195]    [Pg.86]    [Pg.202]    [Pg.226]    [Pg.193]    [Pg.173]    [Pg.306]    [Pg.82]    [Pg.116]    [Pg.566]    [Pg.315]    [Pg.168]    [Pg.712]    [Pg.2506]    [Pg.776]    [Pg.126]   


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Organic surfaces

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