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Immobilized, concentration

Substance Partition coefficient olive oil water Minimal immobilizing concentration. mol/1 (water)... [Pg.24]

K. M. Maness, R. H. Terrill, T. J. Meyer, R. W. Murray, R. M. Wightman, Solid-state diode-like chemiluminescence based on serial, immobilized concentration gradients in mixed-valent poly[Ru(vbpy)(3)](PFg)(2) Ulrns, Journal of the American Chemical Society 1996, 118, 10609. [Pg.59]

Kapur, T.A. and Shoichet, M.S., Immobilized concentration gradients of nerve growth factor guide neurite outgrowth, /. Biomed. Mater. Res. A 68A, 235 3, 2004. [Pg.515]

An electrode that responds to the concentration of a substrate by reacting the substrate with an immobilized enzyme, producing an ion that can be monitored with an ion-selective electrode. [Pg.484]

Potcntiomctric Biosensors Potentiometric electrodes for the analysis of molecules of biochemical importance can be constructed in a fashion similar to that used for gas-sensing electrodes. The most common class of potentiometric biosensors are the so-called enzyme electrodes, in which an enzyme is trapped or immobilized at the surface of an ion-selective electrode. Reaction of the analyte with the enzyme produces a product whose concentration is monitored by the ion-selective electrode. Potentiometric biosensors have also been designed around other biologically active species, including antibodies, bacterial particles, tissue, and hormone receptors. [Pg.484]

By changing the enzyme and mediator, the amperometric sensor in Figure 11.39 is easily extended to the analysis of other substrates. Other bioselective materials may be incorporated into amperometric sensors. For example, a CO2 sensor has been developed using an amperometric O2 sensor with a two-layer membrane, one of which contains an immobilized preparation of autotrophic bacteria. As CO2 diffuses through the membranes, it is converted to O2 by the bacteria, increasing the concentration of O2 at the Pt cathode. [Pg.520]

Directions for preparing a potentiometric biosensor for penicillin are provided in this experiment. The enzyme penicillinase is immobilized in a polyacrylamide polymer formed on the surface of a glass pH electrode. The electrode shows a linear response to penicillin G over a concentration range of 10 M to 10 M. [Pg.534]

Immunoaffinity chromatography utilizes the high specificity of antigen—antibody interactions to achieve a separation. The procedure typically involves the binding, to a soHd phase, of a mouse monoclonal antibody which reacts either directly with the protein to be purified or with a closely associated protein which itself binds the product protein. The former approach has been appHed in the preparation of Factor VIII (43) and Factor IX (61) concentrates. The latter method has been used in the preparation of Factor VIII (42) by immobilization of a monoclonal antibody to von WiHebrand factor [109319-16-6] (62), a protein to which Factor VIII binds noncovalenfly. Further purification is necessary downstream of the immunoaffinity step to remove... [Pg.529]

Eig. 5. Determination of the for the binding of DAS to its polyclonal antibody raised in mice. A fixed amount of immobilized antibody in a microtiter plate is reacted with increasing amounts of DAS and the amount of DAS bound at each concentration is deterrnined using an EIA based on alkaline... [Pg.25]

The concentration requited to displace 50% of aDAS—AP bound to immobilized DAS. [Pg.26]

In a second example, a cell—gelatin mixture is cross-linked with glutaraldehyde (43). When soluble enzyme is used for binding, the enzyme is first released from the cell, then recovered and concentrated. Examples of this type of immobilization include binding enzyme to a DEAE-ceUulose—titanium dioxide—polystyrene carrier (44) or absorbing enzyme onto alumina followed by cross-linking with glutaraldehyde (45,46). [Pg.294]

The response of the immobilized enzyme electrode can be made independent of the enzyme concentration by using a large excess of enzyme at the electrode surface. The electrode response is limited by the mass transport of the substrate. Using an excess of enzyme often results in longer electrode lifetimes, increased linear range, reduced susceptibiUty to pH, temperature, and interfering species (58,59). At low enzyme concentrations the electrode response is governed by the kinetics of the enzyme reaction. [Pg.103]

The dye is excited by light suppHed through the optical fiber (see Fiber optics), and its fluorescence monitored, also via the optical fiber. Because molecular oxygen, O2, quenches the fluorescence of the dyes employed, the iatensity of the fluorescence is related to the concentration of O2 at the surface of the optical fiber. Any glucose present ia the test solution reduces the local O2 concentration because of the immobilized enzyme resulting ia an iacrease ia fluorescence iatensity. This biosensor has a detection limit for glucose of approximately 100 ]lM , response times are on the order of a miaute. [Pg.110]

When selecting a suitable feed symp, the main criteria are optimization of enzyme productivity and minimization of the formation of by-products. Typical feed symp specifications are shown in Table 5. Higher symp concentration and higher viscosity results in a reduced isomerization rate due to diffusion resistance in the pores of the immobilized enzyme. A deaeration step is desirable to remove dissolved oxygen that would otherwise iacrease the formation of by-products. The pH is adjusted to the optimum level for the productivity of the enzyme. [Pg.298]

Electrodecantation or electroconvec tion is one of several operations in which one mobile component (or several) is to be separated out from less mobile or immobile ones. The mixture is introduced between two vertical semipermeable membranes for separating cations, anion membranes are used, and vice versa. When an electric field is apphed, the charged component migrates to one or another of the membranes but since it cannot penetrate the membrane, it accumulates at the surface to form a dense concentrated layer of particles which will sink toward the bottom of the apparatus. Near the top of the apparatus immobile components will be relatively pure. Murphy [J. Electrochem. Soc., 97(11), 405 (1950)] has used silver-silver chloride electrodes in place of membranes. Frilette [J. Phys. Chem., 61, 168 (1957)], using anion membranes, partially separated and Na, ... [Pg.2007]

ANALYTICAL APPLICATION OF SILICAS WITH COVALENT AND ION-EXCHANGE BONDING OF IMMOBILIZED ORGANIC COMPOUNDS FOR SELECTIVE PRE-CONCENTRATION AND DETERMINATION OF PHENOLIC POLLUTANTS... [Pg.254]


See other pages where Immobilized, concentration is mentioned: [Pg.572]    [Pg.698]    [Pg.58]    [Pg.572]    [Pg.43]    [Pg.45]    [Pg.245]    [Pg.6717]    [Pg.351]    [Pg.1366]    [Pg.572]    [Pg.698]    [Pg.58]    [Pg.572]    [Pg.43]    [Pg.45]    [Pg.245]    [Pg.6717]    [Pg.351]    [Pg.1366]    [Pg.2490]    [Pg.610]    [Pg.664]    [Pg.772]    [Pg.135]    [Pg.331]    [Pg.8]    [Pg.299]    [Pg.311]    [Pg.456]    [Pg.476]    [Pg.294]    [Pg.294]    [Pg.404]    [Pg.574]    [Pg.108]    [Pg.110]    [Pg.233]    [Pg.2150]    [Pg.72]    [Pg.124]    [Pg.159]    [Pg.269]   


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