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Molecular error filter

Positive cooperativity is a basic characteristic of molecular amplification devices, since once initiated, the subsequent steps of the assembly are facilitated. It represents a non-linear process and confers features of an error filter, only the correct input will in principle lead to the cooperative structure generation. [Pg.142]

Errors in the molecular weight data from HPSEC are usually due to improperly prepared samples, column dispersity, or flow rate variations. The sample to be analyzed should be completely dissolved in the mobile phase and filtered prior to injection onto the column. A plugged column inlet frit will invalidate results. In addition, do not load the column with excess sample. Column overloading affects the accuracy of data by broadening peaks, reducing resolution, and increasing elution volume. For best results, the concentration of the injected sample should be as low as possible while still providing adequate... [Pg.82]

The fractions coilected are each run dropwise into 100 ml of stirred methanol to which two drops of concentrated hydrochloric acid have been added.Turbidity or precipitation will be observed from about the 6th fraction to about the 20th fraction.The precipitated fractions are filtered off, washed with methanol and dried to constant weight in vacuum at 20 °C. For each fraction the viscosity is measured in water at 25 °C using a capillary viscometer (capillary diameter 0.35 mm) and at as high a concentration as possible (10 g/l) in order to minimize errors.The limiting viscosity number, and hence the molecular weight, is estimated (see Sect. 2.3.3.3.1). Adjacent fractions for which there may be insufficient material for a viscosity measurement,can be combined where necessary. [Pg.177]

FIGURE 6.16 Correlation between calculated and predicted molecular polarizability for 50 benzene derivatives encoded with one-stage filtered D2Q transformed Cartesian RDF (128 components). The standard deviation of the prediction error is 0.6 A. ... [Pg.200]

Extensions of Kalman filters and Luenberger observers [131 Solution polymerizations (conversion and molecular weight estimation) with and without on-line measurements for A4w [102, 113, 133, 134] Emulsion polymerization (monomer concentration in the particles with parameter estimation or not (n)) [45, 139[ Heat of reaction and heat transfer coefficient in polymerization reactors [135, 141, 142] Computationally fast, reiterative and constrained algorithms are more robust, multi-rate (having fast/ frequent and slow measurements can be handled)/Trial and error required for tuning the process and observation model covariance errors, model linearization required The number of industrial applications is scarce A critical article by Wilson eta/. [143] reviews the industrial implementation and shows their experiences at Ciba. Their main conclusion is that the superior performance of state estimation techniques over open-loop observers cannot be guaranteed. [Pg.335]

The only known inborn error of metabolism that can be linked to a copper-dependent enzyme is albinism, A genetically acquired absence of the enzyme tyrosinase results in albinism, which is characterized by the complete lack of pigmentation in the eyes and integument. Tyrosinase is essential in the pigmentation process because this enzyme catalyzes the first two steps in the synthesis of melanin pigment from tyrosine. Mammals that lack pigment do not have the capability to filter the sun s ultraviolet rays, which penetrate the integument and cause molecular havoc. [Pg.131]

Figure 4. Kinetics of the staurosporine-induced increase in tau protein levels.One day before the experiment, PC 12 cells were plated on 20-cm dishes coated with collagen/polylysine and treated with staurosporine (50 nM) or NGF (50 ng/ml) as indicated. After treatment, cells were harvested, lysed and subjected to electrophoresis on 10% SDS-PAGE, electrotransferred to nitrocellulose filters, and immunostained with anti-tau antibody and ECL detection system. (A) A representative Western blot autoradiograph of PC 12 cell cultures treated with staurosporine or NGF. Numbers on top of the autoradiograph indicate hours of treatment. Arrows indicate mobility of rainbow-colored molecular weight markers. (B) Quantitation of tau protein levels by laser densitometry in four different kinetic experiments. Levels of 55- and 110-kD tau proteins were analyzed separately. Values (mean standard error) represent tau proteins level in the treated cells relative to their level in unstimulated control cells. Figure 4. Kinetics of the staurosporine-induced increase in tau protein levels.One day before the experiment, PC 12 cells were plated on 20-cm dishes coated with collagen/polylysine and treated with staurosporine (50 nM) or NGF (50 ng/ml) as indicated. After treatment, cells were harvested, lysed and subjected to electrophoresis on 10% SDS-PAGE, electrotransferred to nitrocellulose filters, and immunostained with anti-tau antibody and ECL detection system. (A) A representative Western blot autoradiograph of PC 12 cell cultures treated with staurosporine or NGF. Numbers on top of the autoradiograph indicate hours of treatment. Arrows indicate mobility of rainbow-colored molecular weight markers. (B) Quantitation of tau protein levels by laser densitometry in four different kinetic experiments. Levels of 55- and 110-kD tau proteins were analyzed separately. Values (mean standard error) represent tau proteins level in the treated cells relative to their level in unstimulated control cells.

See other pages where Molecular error filter is mentioned: [Pg.134]    [Pg.92]    [Pg.9]    [Pg.231]    [Pg.54]    [Pg.93]    [Pg.152]    [Pg.26]    [Pg.125]    [Pg.89]    [Pg.267]    [Pg.48]    [Pg.30]    [Pg.128]    [Pg.294]    [Pg.304]    [Pg.354]    [Pg.361]    [Pg.178]    [Pg.356]    [Pg.359]    [Pg.176]    [Pg.6565]    [Pg.184]    [Pg.467]    [Pg.119]    [Pg.71]    [Pg.789]    [Pg.463]    [Pg.178]    [Pg.185]   
See also in sourсe #XX -- [ Pg.142 ]




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