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Specifications, cell

Figure Bl.24.17. An example of scanning transmission ion microscopy (STIM) measurements of a human oral cancer cell. The different images indicate different windows in the energy of transmitted helium ions as indicated in the figure. White indicate areas of high counts. The teclmique offers a thickness scan through the sample, and, in this case, the cell walls of one specific cell can be seen in the areas dominated by thicker structures (data from C A Pineda, National Accelerator Centre, Fame, South Africa). Figure Bl.24.17. An example of scanning transmission ion microscopy (STIM) measurements of a human oral cancer cell. The different images indicate different windows in the energy of transmitted helium ions as indicated in the figure. White indicate areas of high counts. The teclmique offers a thickness scan through the sample, and, in this case, the cell walls of one specific cell can be seen in the areas dominated by thicker structures (data from C A Pineda, National Accelerator Centre, Fame, South Africa).
A new field of transfusion medicine, cell therapy, has developed with the better understanding of the function of different cell types ia the body. In cell therapy, various malignancies are treated by transfusion of specific cell types from blood. Therefore, more and more specialized methods for separating blood iato the various components are required. [Pg.520]

The two principal appHcations of countercurrent flow are found in the Beckman elutriators and the Haemonetics apheresis equipment. The Beckman elutriators are capable of very specific cell separation of small batches of cells. The Haemonetics surge technique can separate platelets and lymphocytes from four Hters of donor blood in one hour and forty minutes. [Pg.522]

Beckman Elutriation Method. The Beckman elutriation method uses a chamber designed so that the centrifugal effect of the radial inward fluid flow is constant (Fig. 3). The separation chambers are made of transparent epoxy resin which faciUtates observation of the movements of the cell boundary in strobe light illumination. This enables detection of the radius at which the cells are separating. When a mixture of cells, eg, mononuclear white cells, enters the chamber, separation can be achieved by fine tuning centrifuge speed and inward fluid flow to the specific cell group. This is a laboratory method suitable for relatively small numbers of cells. Chambers are available in sizes to handle 2-3 x 10 , 1 2 x 10 , and 1 x 10 ° cells. The Beckman chambers can be appHed to collect mononuclear cells from bone marrow aspirates. [Pg.522]

The primary use of EIA when it was first developed was for histological labeling and localization of specific cell macromolecules. Eor example, enzymes labeled with peroxidase were used to locate specific cellular compartments and stmctures for microscopic examination. The flexibiUty of EIA was recognized quickly and it was adapted for use as a laboratory assay. [Pg.24]

EIA was originally developed as a histological technique to localize specific ceUular sites using the specificity of an immunological reaction (23). The resulting fluorescent antibodies can be detected in animal tissues at levels as low as 1 /tg/mL of body fluid. Eluorophore-labeled antibodies have also been used widely for flow cytometry appHcations using fluorescein antibodies to cell surface markers to detect and quantify specific cells (24). [Pg.26]

Producers have developed specific cell configurations to optimise electricity consumption, cell capital, and operating costs. Pacific Engineering Corp., Kerr-McGee Chemical Corp., Chedde Pechiney, Cardox Corp., Electrochemie Turgi, American Potash and Chemical, and I. G. Earbenindustrie each has a unique cell design. [Pg.68]

Reaction Mechanisms. There is considerable difference of opinion concerning the specific cell reactions that occur ia the silver—ziac battery. Equations that are readily acceptable are... [Pg.554]

The mechanical properties of natural fibers depend on cellulose type because each type of cellulose has a specific cell geometry and the geometrical conditions determine the mechanical properties. [Pg.792]

Interference with specific cell-cell and cell-matrix adhesion mechanisms is another rapidly advancing approach to therapeutically interfere with angiogenesis. Antagonistic antibodies (Vitaxin) to the integrin heterodimer av 33 have been shown to act on the blood vessels of tumors but not on the resting organ vasculature. Vitaxin demonstrated some promise in Phase II clinical trials. [Pg.87]

Cellular therapies in transplantation and cancer are based on specific cells separated or sorted from human blood, bone marrow, or cord blood by means of their specific cell surface markers or cell differentiation antigens, e.g., CD3, CD4, CD8, CD 14, CD 19, and CD34. For example, the CD34+ stem cells, especially those derived from human embryos, have the capacity to differentiate in culture to generate different somatic cells, e.g., liver cells, heart cells, neurons, etc. This exploding field of research is now termed regenerative medicine. [Pg.265]

The steroid hormone 1,25-dihydroxy vitamin D3 (calcitriol) slowly increases both intestinal calcium absorption and bone resorption, and is also stimulated through low calcium levels. In contrast, calcitonin rapidly inhibits osteoclast activity and thus decreases serum calcium levels. Calcitonin is secreted by the clear cells of the thyroid and inhibits osteoclast activity by increasing the intracellular cyclic AMP content via binding to a specific cell surface receptor, thus causing a contraction of the resorbing cell membrane. The biological relevance of calcitonin in human calcium homeostasis is not well established. [Pg.279]

In addition to pharmacological approach, HO expression can also be downregulated by HO antisense treatment. Once the antisense is tagged to a specific cell type, cell type-specific local production of CO can be inhibited, which is more advantageous than general inhibition of HO activity by pharmacological compounds. [Pg.324]

A cell diagram corresponds to a specific cell reaction in which the right-hand electrode in the cell diagram is treated as the site of reduction and the left-hand electrode is treated as the site of oxidation. The sign of the emf then distinguishes whether the resulting reaction is spontaneous in the direction written ( > 0) or whether the reverse reaction is spontaneous ( < 0). [Pg.617]

Luminescence yields data that often cannot be provided by any other methodology. This book is a compilation of a wide variety of original research contributions. Substantial information is given on the use of luminescence techniques to understand specific cell responses and the chemical mechanisms of cell action. An examination of natural environments is presented in the form of specific studies that characterize materials in both solid and liquid form and give information on the respective reactions of these materials in soil and water systems. Advanced research on standardization and standards developed for luminescence studies, as well as both active and passive use of luminescence, is included. [Pg.258]

Engler AJ, Sen S, Sweeney HL, Discher DE (2006) Matrix elasticity directs stem cell lineage specification. Cell 126 677-689... [Pg.167]

Of the thousands of different enzymes present in the human body, those that fulfill functions indispensable to cell vitality are present throughout the body tissues. Other enzymes or isozymes are expressed only in specific cell types, during certain periods of development, or in response to specific physiologic or pathophysiologic changes. Analysis of the presence and distribution of enzymes and isozymes— whose expression is normally tissue-, time-, or circumstance-specific—often aids diagnosis. [Pg.56]

T cells responsible for delayed-type hypersensitivity seerete lymphokines whieh recruit and activate non-specific cells like maerophages into the area of the reaetion. Examples of some of these lymphokines are listed below. [Pg.295]


See other pages where Specifications, cell is mentioned: [Pg.1846]    [Pg.2834]    [Pg.2844]    [Pg.32]    [Pg.406]    [Pg.302]    [Pg.149]    [Pg.544]    [Pg.250]    [Pg.332]    [Pg.154]    [Pg.238]    [Pg.588]    [Pg.614]    [Pg.889]    [Pg.1316]    [Pg.419]    [Pg.197]    [Pg.71]    [Pg.256]    [Pg.143]    [Pg.145]    [Pg.331]    [Pg.157]    [Pg.542]    [Pg.435]    [Pg.456]    [Pg.610]    [Pg.355]    [Pg.234]    [Pg.235]    [Pg.74]    [Pg.103]   


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Antigen-specific T cell activation

Antigen-specific Treg cells

Aqueous Fuel Cell Using Specific Electrolyte

Autoantigens, /3-cell specific

B-cell specific activator protein

Cell cycle-specific drug

Cell specific growth rates

Cell specificity

Cell specificity

Cell type-specific coregulators

Cell type-specific gene expression

Cell wall specific gravity

Cell wall synthesis inhibitors specific agents

Cell-cycle specific agent

Cell-cycle specificity

Cell-cycle specificity, cytotoxic drugs

Cell-specific drag targeting, examples

Cell-specific drug delivery

Cell-specific signaling

Cell-surface receptor proteins specificity

Cell-type specific proteins

Cell-type specific surface markers

Cell-type specificity

Cells specific energy

Chemotherapy cell-cycle specificity

Cytotoxic agents cell-cycle-specific

Dendritic cell-specific intracellular

Double-Layer Specific Capacitance Characterization Using Three-Electrode Cell

Double-Layer Specific Capacitance Characterization Using Two-Electrode Test Cell

Drug action, cell cycle specificity

Endothelial cell specific promoter

Eukaryotic cells, specific enzyme production

Expression of cell-type specific proteins

Fuel cell critical specifications

Fuel cell power plants design specifications

Generation of Ag-Specific Cell-Mediated Responses

Genetic Mechanisms in Formation and Specification of Founder Cells

Germ cell specific toxicants, male

Half-cells specific types

Hematopoietic cell lineage-specific

High-Power Fuel Cells for Satellites with Specific Missions

Host Cell-Specific Interactions

Lead-acid cell specific energy

Listeria-specific cell mediated

Listeria-specific cell mediated immunity

Nerve growth factor cell specificity

Neural Cell-Specific Markers

Non-specific cytotoxic cells

Operating specifications, cell room

Other specific biochemical markers for Purkinje cells

Phage display cell-specific targeting

Photoreceptor cell-specific receptor

Pigment cell-specific gene expression

Precursor cells lineage-specific

Purkinje cell specific

Purkinje cell specific glycoprotein

Restricted cell-type specificity of immunoglobulin gene transcription

Site-specific drug delivery cell targeting

Solar cell specifications

Specific Energy Consumption and Cell Voltage

Specific Half-Cells and Reference Electrodes

Specific activity, platinum fuel cell

Specific activity, platinum fuel cell electrocatalysts

Specific cell-mediated cytotoxicity

Specific conductivity, fuel cell electrolyte

Specific power, fuel cell

Specific power, fuel cell methods

Specific power, fuel cell performances achieved

Specifications diaphragm cells

Specifications membrane cells

Specifications mercury cells

Storage tissue-/cell specific

Targeting Drug Delivery to Specific Cells and Tissues

Targeting specific cells in the kidney

Thyroid hormones cell specificity

Tissue (Cell Type)-Specific Expression

Tissue-specific progenitor cells

Transporters cell-specific

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