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CS, activation

Fig. XVII-29. Nitrogen isotherms the volume adsorbed is plotted on an arbitrary scale. The upper scale shows pore radii corresponding to various relative pressures. Samples A, Oulton catalyst B, bone char number 452 C, activated charcoal F, Alumina catalyst F12 G, porous glass S, silica aerogel. (From Ref. 196). Fig. XVII-29. Nitrogen isotherms the volume adsorbed is plotted on an arbitrary scale. The upper scale shows pore radii corresponding to various relative pressures. Samples A, Oulton catalyst B, bone char number 452 C, activated charcoal F, Alumina catalyst F12 G, porous glass S, silica aerogel. (From Ref. 196).
Protein C activator pLOOD, COAGULANTS AND ANTICOAGULANTS] (Vol 4) Thromboplastin [9002-05-5]... [Pg.991]

Type Temperature for a half-life of 1 s, °C Activation energy, kJ/mol Active oxygen, %... [Pg.375]

As a result of having two chiral centers, four stereoisomers of ascorbic acid are possible (Table 1) (Fig. 2). Besides L-ascorbic acid (Activity = 1), only D-araboascorbic acid (erythorbic acid (9)) shows vitamin C activity (Activity = 0.025-0.05). The L-ascorbic acid stmcture (1) in solution and the soHd state are almost identical. Ascorbic acid crystallizes in the space group P2 with four molecules in the unit cell. The crystal data are summarized in Table 2. [Pg.11]

In apphcations where vitamin C activity is unimportant, often D-erythorbic acid (D-araboascorbic acid) can also be used, providing the same antioxidant and reducing properties as L-ascorbic acid. [Pg.18]

Nl pyrazoles NMR Coalescence temperature (°C) Activation energy (kJmoP ) Ref. [Pg.213]

Economy, J., Daley, M. and Mangun. C., Activated carbon fibers - past, present and future, ACS Preprints (Fuel Chemistry Division), 1996, 41(1), 321 325. [Pg.111]

Protein kinase A activation usually promotes, whereas protein kinase C activation retards, apoptosi.s. [Pg.285]

Structural basis of protein kinase C activation by heterocyclic tumor promoters 98ACR163. [Pg.238]

The structure of human muscle fructose-1,6-bisphosphate aldolase, as determined by X-ray crystallography and downloaded from the Protein Data Bank. (PDB ID 1ALD Gamblin, S. J., Davies, G. J., Grimes, J. M., Jackson, R. M., Littlechild, J. A., Watson, H. C. Activity and specificity of human aldolases. J. Mol. Biol. v219, pp. 573-576, 1991.)... [Pg.865]

The NHR contains also the conserved Calcineurin docking site, PxlxIT, required for the physical interaction of NEAT and Calcineurin. Dephosphorylation of at least 13 serines residues in the NHR induces a conformational change that exposes the nuclear localization sequences (NLS), allowing the nuclear translocation of NEAT. Rephosphorylation of these residues unmasks the nuclear export sequences that direct transport back to the cytoplasm. Engagement of receptors such as the antigen receptors in T and B cells is coupled to phospholipase C activation and subsequent production of inositol triphosphate. Increased levels of inositol triphosphate lead to the initial release of intracellular stores of calcium. This early increase of calcium induces opening of the plasma membrane calcium-released-activated-calcium (CRAC) channels,... [Pg.847]

Turbidity measurements were determined using the dipping probe colorimeter. The light frequency was 650 nm. Deionized water transmittance was set at 90. The surfactant test solutions were stirred ( — 3500 rpm) and maintained at 75°C. Active surfactant concentration was 0.1% wt. Solution volume was 100 cm1. A 26.5% CaCU (95,699 ppm CaJ+) solution was added via syringe in 0,10 ml increments to the lower portion of the surfactant solution. [Pg.379]

Frequency Factor (1, mole, sec) Activation Energy/R (°c) Activation Volume/R (°C/atmo)... [Pg.225]

C. Active magnesium. A 200-ml., three-necked, round-bottomed flask is equipped with a Teflon-coated magnetic stirring bar, stopper, rubber septum, and condenser connected to an argon inlet (Note 6). The flask is charged with 1.5 g. (0.038 mole) of freshly cut potassium (Notes 7 and 8), 2.01 g. (0.0211 mole) of anhydrous magnesium chloride (Note 9), 3.55 g. (0.0214 mole) of anhydrous potassium iodide (Note 10), and 50 ml. of tetrahydrofu-ran (Note 11). The mixture is stirred vigorously (Note 12) and... [Pg.44]

The results do not differentiate between C activity derived from TCDD and that of possible metabolites. However, small amounts of C activity were detected in the expired air and urine within the first 10 days following administration. This is evidence that some metabolic alteration or breakdown of TCDD occurs. [Pg.90]

Thus far, all examples of C—C activation and/or C—C formation have employed alkynes, either alone or in concert with cluster-bound alkylidyne or CO. [Pg.69]

C—C activation. C C formation 2 PhC-CPh CPh + CPhCPhCPh IWCIiot/ti-CPhll-CPhCPhCPh M/(-CO)2(COla() -C3lH) butterfly 77. 78... [Pg.70]

The a subunits and the Py complex have actions independent of those on adenylyl cyclase (see Figure 43-4 and Table 43-3). Some forms of tt stimulate channels and inhibit Ca channels, and some ttj molecules have the opposite effects. Members of the G, family activate the phospholipase C group of enzymes. The py complexes have been associated with channel stimulation and phospholipase C activation. G proteins are involved in many important biologic processes in addition to hormone action. Notable examples include olfaction (oColf) <1 vision (aj. Some examples are listed in Table 43-3. GPCRs are implicated in a number of diseases and are major targets for pharmaceutical agents. [Pg.459]

Protein C Activated to protein Ca by thrombin bound to thrombomodulin then degrades factors Villa and Va. [Pg.600]

The differences between palytoxin and PDBu with respect to kinetics, temperature dependence, and effect on low affinity binding suggest that these two different types of tumor promoters may be acting through different mechanisms. Further, in contrast to PDBu, the effect of palytoxin is not readily reversible (33). To determine where the two pathways differ, we compared the relative ability of palytoxin and PDBu to inhibit EGF binding in protein kinase C depleted cells. Swiss 3T3 cells were depleted of protein kinase C to different extents by exposing confluent quiescent cells to 0, 20, 200, or 2000 nM PDBu for 72 hr. Previous results indicate that this treatment depletes cells of protein kinase C activity in a dose-dependent manner (31). [Pg.207]

Fig. 1. Performance evaluation of prepared electro-catalysts as an electrode of PEMFC. Cell temperature 70 C, active area 50cm, platinum loading anode(0.3mgPt/cm )/cathode(0.45mg Pt/cm ), fuel utilization H2/O2 = 80%/50%, RH 100% RFl, pressure H2/O2 = 0 psig/0 psig. Fig. 1. Performance evaluation of prepared electro-catalysts as an electrode of PEMFC. Cell temperature 70 C, active area 50cm, platinum loading anode(0.3mgPt/cm )/cathode(0.45mg Pt/cm ), fuel utilization H2/O2 = 80%/50%, RH 100% RFl, pressure H2/O2 = 0 psig/0 psig.

See other pages where CS, activation is mentioned: [Pg.71]    [Pg.841]    [Pg.202]    [Pg.299]    [Pg.18]    [Pg.390]    [Pg.175]    [Pg.141]    [Pg.96]    [Pg.152]    [Pg.76]    [Pg.99]    [Pg.506]    [Pg.57]    [Pg.77]    [Pg.343]    [Pg.386]    [Pg.89]    [Pg.675]    [Pg.832]    [Pg.833]    [Pg.1172]    [Pg.520]    [Pg.521]    [Pg.177]    [Pg.361]    [Pg.70]    [Pg.79]    [Pg.530]   
See also in sourсe #XX -- [ Pg.221 ]




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