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Cell process control

The apparatus consists of a temperature regulated chamber, load cell, process controller and recorder. The outside view of the apparatus is shown in Fig. 2. [Pg.329]

Specialized equipment for industrial measurements and automatic control have been developed (18) (see Process control). In general, the pH of an industrial process need not be controlled with great accuracy. Consequendy, frequent standardization of the cell assembly may be uimecessary. On the other hand, the ambient conditions, eg, temperature and humidity, under which the industrial control measurements are made, may be such that the pH meter must be much more robust than those intended for laboratory use. To avoid costiy downtime for repairs, pH instmments may be constmcted of modular units, permitting rapid removal and replacement of a defective subssembly. [Pg.468]

Dielectric Constant The dielectric constant of material represents its ability to reduce the electric force between two charges separated in space. This propei ty is useful in process control for polymers, ceramic materials, and semiconduc tors. Dielectric constants are measured with respect to vacuum (1.0) typical values range from 2 (benzene) to 33 (methanol) to 80 (water). TEe value for water is higher than for most plastics. A measuring cell is made of glass or some other insulating material and is usually doughnut-shaped, with the cylinders coated with metal, which constitute the plates of the capacitor. [Pg.764]

Mercury is emitted from the mercury cell process from ventilation systems and by-product streams. Control techniques include (1) condensation, (2) mist elimination, (3) chemical scrubbing, (4) activated carbon adsorption, and (5) molecular sieve absorption. Several mercury cell (chloralkali) plants in Japan have been converted to diaphragm cells to eliminate the poisonous levels of methyl mercury found in fish (9). [Pg.499]

The ability of the leucine zipper proteins to form heterodimers greatly expands the repertoire of DNA-binding specificities that these proteins can display. As illustrated in Figure 10.19, for example, three distinct DNA-binding specificities could, in principle, be generated from two types of monomer, while six could be created from three types of monomer and so on. This is an example of combinatorial control, in which combinations of proteins, rather than individual proteins, control a cellular process. It is one of the most important mechanisms used by eucaryotic cells to control gene expression. [Pg.193]

It is emphasized that drug activity is observed through a translation process controlled by cells. The aim of pharmacology is to derive system-independent constants characterizing drug activity from the indirect product of cellular response. [Pg.37]

The recorded data can be used to improve the process. Controlling operating conditions is important for maintaining viable cells, and it makes the interpretation of fermentation data easier. [Pg.70]

The very beginning of the first mitotic cell cycle of the mouse embryo seems to be controlled by the mechanisms characteristic for both meiotic and mitotic cell cycles. Active MAP kinase, its substrate p90rsk and the CSF activity itself could influence the cellular processes within the one-cell embryo. Indeed, we have observed that despite the entry into the interphase (as judged by the low activity of MPF) some proteins are actively phosphorylated as during the meiotic M phase (e.g. 35 kDa complex Howlett et al 1986, Szollosi et al 1993), the nuclei and the microtubule interphase network start to form only 1.5 hours after activation (Szollosi et al 1993). This delay in the phenomena characteristic for the interphase could be linked to the mixed meiotic/mitotic character of this early period. This delay probably allows the correct transformation of the sperm nucleus into the male pronucleus. In species like Xenopus or Drosophila the transitional period between the meiotic and the mitotic cell cycle control is probably much shorter since it is proportional to duration of the short first cell cycle of these rapidly cleaving embryos. Mammalian embryos are perhaps the most suitable to study this transition because of the exceptionally long first embryonic cell cycle. [Pg.83]

Poly(3HB) is usually produced in a batch or fed-batch regime. These types of process control are derived from the general observation that overproduction of poly(3HB) occurs when cell multiplication is limited by an essential nutrient and the carbon substrate is available in excess. Batchwise production has an advantage in that a high poly(3HB) content can be reached. One disadvantage is the quality of the product, which can vary from one batch to the next. This can be overcome by a continuous process. Continuous production is basically possible if ... [Pg.153]

While we recommend the application of control cell fines as reagent, assay, and EQA monitoring tools, it is important to emphasize that appropriate tissue controls are also continued to be used in parallel, as tissue is still considered the gold standard in laboratory assay control. For reliable results, it is also important that tissue or cell line controls are fixed and processed in the same manner as diagnostic material submitted for evaluation. [Pg.102]


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