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Folding, PDAs

A PDA detector provides UV spectra of eluting peaks in addition to monitoring the absorbance of the HPLC eluent like the UVA is absorbance detector. It is the preferred detector for testing impurities and for method development. PDA facilitates peak identification during methods development and peak purity evaluation during method validation. Detector sensitivity was an issue in earlier models but has improved significantly (more than ten-fold) in recent years. ... [Pg.65]

Serum previously stored at -80 °C was freshly thawed and diluted 3,500 fold using PBS-T (0.02% Tween 20 in PBS). An aqueous alachlor standard or unknown sample was preincubated with an equal volume of diluted serum at 22 °C for 1 hour. This mixture (0.1 mL/well) was then dispensed into six replicate wells on the plate, which was then covered and incubated at 22 °C for 1.5 hours. After triplicate washes of the wells with PBS-T, each well was treated with 0.1 mL of GAR-HRP (freshly thawed and diluted 4,000 fold with 1.0% powdered milk in PBS). After a final cycle of four washes with PBS-T, 0.2 mL of freshly prepared PDA substrate solution (0.4 mg/mL PDA and 0.01% H2O2 in 0.05 M citric acid containing 0.15 M sodium dibasic phosphate, pH 5.0) was dispensed into each of the wells and incubated in the dark at 22 °C for 30-60 minutes. Sulfuric acid (4 N, 0.05 mL/well) was added to stop the reaction, and the final absorbance of each well (490 nm) was recorded. The presence of free alachlor in samples inhibited the binding of the antibody to alachlor-BSA, resulting in an inhibition of the development of absorbance at 490 nm. The amount of free alachlor was thus inversely proportional to the intensity of color produced. The level of alachlor in unknown water samples was calculated based on alachlor standards which had been analyzed simultaneously on each plate. Alachlor standards (0, 0.2, 0.5, 1.0, 3.0, 5.0, and 8.0 ppb in deionized water) were stored at -20 °C in 1 mL portions, and were freshly thawed for each assay. [Pg.183]

While it may be expected that the interchain separation will be a function of the length of the pendant sidechain, the relation is unlikely to be linear. For example, folding becomes more likely with an increasing number of constituents in the methylene chains connecting the urethane functional group to the polymer spine. Upper bounds on the interchain distances for the PDAs investigated are given in Table II. [Pg.161]

One pre-requisite for such estimates is that all measured particles are spherical. This may be obtainable in modeled flows with selected particles, but is certainly not the rule in practical situations. The instrumentation problem is therefore two-fold. If the PDA system can detect non-sphericity, as indicated above using a three-detector receiver, then as a minimum the mass contained in all rejected non-spherical particles will be missed. If on the other hand, many non-spherical particles are in fact accepted as spherical particles, their computed size may differ from the volume equivalent diameter of a spherical droplet, thus also falsifying the measured mass flux. [Pg.295]

Optimum enzyme activity was observed over a broad pH range, from pH 6.8 to 9.0. The enzyme has a K, of 190 p,M for its substrate, 12-oxo-PDA. The preferred reductant was NADPH, for which the enzyme exhibited a K, of 13 i,M, compared with 4.2 mM for NADH. Reductase activity was low in the com kernel but increased five-fold by the fifth day after germination and then gradually declined [37]. [Pg.272]

PDA liposomes usually have lipids with two alkyl chains but liposomes can be formulated with a single or multiple alkyl chains in the lipids. The length and number of the lipid tails controls the self-assembly process of the amphiphiles in addition to the transition temperature from crystalline to liquid chain packing. It has also been observed that an increase in the size of the chains results in a red color upon polymerization. PDA polymers that have nonequivalent tails are 6500-fold less efficient at polymerization than those of the corresponding equivalent two-tailed monomers The increase in efficiency of two-tailed monomers is likely the result of better alignment for more optimal geometry. [Pg.271]

The introduction of vehicles implementing rechargeable batteries has increased the demand for batteries by several-fold. Batteries remained the mainstream source of power for systems ranging from mobile phones and personal digital assistants (PDAs) to electric and hybrid electric vehicles. The world market for batteries was approximately 41 billion in 2000, which included 16.2 billion primary and 24.9 billion secondary cells [20]. In 2010, the global demand was placed at 71 billion. [Pg.137]

In the presence of a 3-fold excess of sacrificial 2-methylpropanal, Co(acac)2 effects the aerobic oxidative cleavage (Figure 57) of (+)- and (-)-pinanediols (PDa,b) to the enantiomerically pure (+)- and (-)-cis-pinonic acids (PAajb) . In 1,2 dichloroethane at room temperature, 88% yield was observed in a reaction time of 6 hours. [Pg.310]


See other pages where Folding, PDAs is mentioned: [Pg.238]    [Pg.316]    [Pg.227]    [Pg.152]    [Pg.91]    [Pg.2473]    [Pg.253]    [Pg.238]    [Pg.221]    [Pg.99]    [Pg.748]    [Pg.100]    [Pg.144]    [Pg.205]   
See also in sourсe #XX -- [ Pg.161 ]




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