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Cell hybrids

Porous nickel diom pores mox) f Porous nickel 30 t diom pores (approx) [Pg.165]

The most successful fuel cell to date is the hydrogen-oxygen fuel cell, which deserves special attention since it has been used in the Apollo and Gemini space flights and moon landings. The reaction [Pg.165]

To facilitate the rapid attainment of equilibrium, a liquid gas-diffusion electrode was developed whereby concentration polarization could be minimized. The ohmic polarization (the RI drop between the electrodes, which gives rise to an internal resistance) is also minimized when the anode-to-cathode separation is reduced. The apparatus of the hydrogen-oxygen fuel cell developed by Bacon with gas-diffusion electrodes is shown in Fig. 9.12. The operating temperature of 240 C is attained with an electrolyte concentration of about 80% KOH solution, which with the high pressures of about 600 psi for H2 and O2, allows high current densities to be drawn with relatively low polarization losses. Units such as these with power of 15 kW have been built and used successfully for long periods. [Pg.165]

fuel cells are still in the development stage, and much further work must be done before an efficient economical fuel cell is produced. The oxidation of coal or oil to CO2 and H2O has been achieved in a fuel cell the system uses platinum as a catalyst and an acid electrolyte at high temperature, and thus the cost of materials for the cell construction is very high. The economic fuel cell-powered automobile, although a distinct possibility, is not to be expected in the immediate future. [Pg.165]

The hybrid cell is one which is not rechargeable by simply reversing the voltage. Some of these use oxygen in air as the cathode material [Pg.165]


Mammalian Cells Unlike microbial cells, mammalian cells do not continue to reproduce forever. Cancerous cells have lost this natural timing that leads to death after a few dozen generations and continue to multiply indefinitely. Hybridoma cells from the fusion of two mammalian lymphoid cells, one cancerous and the other normal, are important for mammalian cell culture. They produce monoclonal antibodies for research, for affinity methods for biological separations, and for analyses used in the diagnosis and treatment of some diseases. However, the frequency of fusion is low. If the unfused cells are not killed, the myelomas 1 overgrow the hybrid cells. The myelomas can be isolated when there is a defect in their production of enzymes involved in nucleotide synthesis. Mammahan cells can produce the necessary enzymes and thus so can the fused cells. When the cells are placed in a medium in which the enzymes are necessaiy for survival, the myelomas will not survive. The unfused normal cells will die because of their limited life span. Thus, after a period of time, the hybridomas will be the only cells left ahve. [Pg.2134]

McLawhon, R.W. West, R.E., Jr. Miller, R.J. and Dawson, G. Distinct high-aff1nity binding sites for benzomorphan drugs and enkephalin in a neuroblastoma-brain hybrid cell line. Proc Natl MM USA, 78 4309-4313, 1981. [Pg.34]

W. Evidence for opioid receptor-mediated activation of the G-proteins, Go and Gi2, in membranes of neuroblastoma x glioma (NG108-15) hybrid cells. J Biol Chem 1991 266 3365-3368. [Pg.484]

Monoclonal antibody technology entails isolation of such B-lymphocytes, with subsequent fusion of these cells with transformed (myeloma) cells. Many of the resultant hybrid cells retain immortal characteristics, while producing large quantities of the monospecific antibody. These hybridoma cells can be cultured long term to effectively produce an inexhaustible supply of the monoclonal antibody of choice. [Pg.376]

Abstract. The hybrid cell lines, which we have obtained, can be widely used in veterinary virology and biotechnology for preparing vaccines, test-systems for viruses. Any strains of hybrid cells are producing the biological active proteins (enzymes and others). We have obtained hybrid cell lines (PO-TKxCO, PO-TKxHO), which are sensitive to prion protein, and also hybrid culture with P-cells of the pancreas of rabbit. [Pg.211]

The new trend of hybridization is the obtaining of hybrid cell cultures of domestic animals, which develops since the beginning of 1980-ies in the laboratory of cell biotechnology at the Institute of experimental veterinary (L. P. Djakonov, A. A. Kusch, T. M. Tugizov, 1985 E. V. Maydzhy, 1987). [Pg.212]

TABLE 2. Intraspecific and interspecific hybrid cells of agricultural animals, obtained in the laboratory of biotechnology (1982 2004)... [Pg.214]

Isolation and characterization of monosomal mouse cell lines and interspecific hybrid cells with single mouse chromosomes... [Pg.20]

Select immortal hybrid cells that produce antibody with high antigen specificity and binding affinity... [Pg.277]

Figure 10.3. Schematic representation of monoclonal antibody production using immortalized hybrid cells that secrete antibodies selective for the target antigen. The mortal, immune B cells Isolated from mice immunized with a target antigen are fused with myeloma, immortal B cells that express defective antibodies. The selecting of antigen-specific, immortal hybrid cells (hybridomas) results in identification of unique clones of cells that express antibodies with high specificity and affinity (monoclonal antibodies). These cells are cloned and expanded for large-scale monoclonal antibody preparations. Figure 10.3. Schematic representation of monoclonal antibody production using immortalized hybrid cells that secrete antibodies selective for the target antigen. The mortal, immune B cells Isolated from mice immunized with a target antigen are fused with myeloma, immortal B cells that express defective antibodies. The selecting of antigen-specific, immortal hybrid cells (hybridomas) results in identification of unique clones of cells that express antibodies with high specificity and affinity (monoclonal antibodies). These cells are cloned and expanded for large-scale monoclonal antibody preparations.
As noted, one of the remaining challenges in obtaining human hybridoma cells for generahng human monoclonal antibodies is the lack of suitable human myeloma cell lines to generate stable hybrid cells that can be cloned and expanded indefinitely in culture. Many human hybridoma... [Pg.277]

Figure 16.1. Schematic representation of the yeast two-hybrid system for evaluation of protein-protein interactions. Haploid yeast of a and a cells can mate to form (a/a) diploid cells. (A) If two test proteins, PT1 and PT2—expressed in (a/a) diploid cells as fusion proteins of DNA binding domains (DAB) and activation domains (AD) of yeast gene-transcript activator proteins—bind to each other, the binding interaction allows the diploid cells to grow in histidine selection media. Histidine selection media is permissive for diploid cells that express the HISS reporter gene only if PT1 and PT2 interact. (B) If PT1 and PT2 do not interact, no HISS gene product is expressed and the hybrid cell cannot grow in histidine media. Figure 16.1. Schematic representation of the yeast two-hybrid system for evaluation of protein-protein interactions. Haploid yeast of a and a cells can mate to form (a/a) diploid cells. (A) If two test proteins, PT1 and PT2—expressed in (a/a) diploid cells as fusion proteins of DNA binding domains (DAB) and activation domains (AD) of yeast gene-transcript activator proteins—bind to each other, the binding interaction allows the diploid cells to grow in histidine selection media. Histidine selection media is permissive for diploid cells that express the HISS reporter gene only if PT1 and PT2 interact. (B) If PT1 and PT2 do not interact, no HISS gene product is expressed and the hybrid cell cannot grow in histidine media.
The development of hybridoma technology by Milstein and Kohler in 1975 revolutionized the antibody field and radically increased the purity and specificity of antibodies used in the clinic and for diagnostic tests in the laboratory. Hybridomas consist of antibody-forming cells fused to immortal plasmacytoma cells. Hybrid cells that are stable and produce the required antibody can be subcloned for mass culture for antibody production. Large-scale fermentation facilities are now used for this purpose in the pharmaceutical industry. [Pg.1194]

Werner R, Levine E, Rabadan-Diehl C, Dahl G Formation of hybrid cell-cell channels. Proc Natl Acad Sci USA 1989 86 5380-5384. [Pg.138]

Fusion with the cells compensates for this deficiency. When fused and unfused cells are incubated in the presence of the folic acid antagonist aminopterin, the de novo synthesis of purines and pyrimidines for DNA is blocked. Cells deficient in HGPRT die, whereas hybrid cells are able to bypass aminopterin blockage by metabolism of hypoxanthine and thymidine added to the medium. In the generation of mouse hybridomas, an number of myelomas deficient in HGPRT are available, all originating from MOPC 21, a spontaneous myeloma from the BALB/c mouse strain. [Pg.71]

In MAB technology, the objective of the fusion process is to produce hybrid cells that incorporate the immortal characteristics of the myeloma cell with the antibody secreting properties of the antigen-sensitized lymphocytes. [Pg.72]

We do not consider the related subject of fuel cells, where both cathodic and anodic reagents - usually gases - are stored externally and can be supplied to the electrochemical cell on a continuous basis. A number of books have recently been published on this topic. The term hybrid cell is used here to describe a power source in which one of the active reagents is in the gaseous state, e.g. the oxygen of the air. Use of the word hybrid in this context should not be confused with its meaning in the phrase hybrid electric vehicle , which refers to an electric vehicle with more than one power supply, as described below. [Pg.3]

A number of cells have been developed which make use of the oxygen of the air as the cathodic reagant. These so-called air-depolarized cells are examples of hybrid cells, which are discussed more fully in Chapter 9. Many recent advances in metal-air batteries can be attributed to the research carried out in the 1960s on high current density air electrodes for ambient hydrogen/oxygen fuel cells using aqueous electrolytes. [Pg.98]


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See also in sourсe #XX -- [ Pg.3 , Pg.290 ]

See also in sourсe #XX -- [ Pg.79 , Pg.80 , Pg.81 , Pg.82 ]




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