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Antibodies system, Antibody synthesis

Related topics The immune system (Dl) Antibody synthesis (D4)... [Pg.105]

Another example of new sorbents is the molecular imprinted polymers (MIP) from the work of Siemann and co-workers (1996). They synthesized a methacrylic acid-ethylene glycol dimethacrylate copolymer with atrazine as an imprint molecule. Imprint synthesis entails polymerization around an imprint species with monomers that are selected for their ability to form specific and definable interactions with the imprint molecule. The atrazine is chemically removed from the polymer leaving holes or cavities. The cavities are formed in the polymer matrix whose size and shape are complementary to that of the imprint molecule (Siemann et al., 1996). These recognition sites enable the polymer to rebind the imprint species selectively from a mixture of closely related compounds, in many instances with binding affinities approaching those demonstrated by antigen-antibody systems. [Pg.321]

The effects of MeHg on lymphocyte function have been studied in cell-culture systems in an attempt to elucidate the mechanisms involved in its ability to modulate immune function. Exposure of cultured lymphocytes to MeHg has been shown to inhibit mitogen-induced DNA synthesis, cell proliferation, and antibody synthesis. Electron micro... [Pg.179]

With regard to the inhibition of primary antibody responses, it may prove difficult to maintain sufficiently high concentrations of low molecular weight hapten in vivo. Thus, N -BPO-N -formyl-L-lysine did not inhibit the primary anti-BPO response to a BPO-BGG conjugate injected intravenously into rabbits, whereas with in vitro induction systems, specific inhibition of anti-hapten antibody responses can be observed in a number of instances. Secondary anti-hapten responses are easier to inhibit and N -BPO-iV" -formyI-L-lysine strikingly abolished anti-BPO antibody synthesis in primed rabbits secondarily injected with BPO-BGG (for review see de Weck 1974),... [Pg.27]

Antibodies are immune system-related proteins called immunoglobulins. An important component of the immune system, antibodies are found in the blood of all vertebrates. The synthesis, or manufacture, of antibodies is initiated when a foreign substance, referred to as an antigen, enters the body. Lymphocyte cells respond to the foreign substance by making an antibody with a molecular arrangement that fits the shape of molecules on the siuface of the substance so that the antibody combines with it. Common antigens are the protein components of bacteria and viruses. [Pg.75]

An application of the Ag -electrode is in the sensitive detection of a protein by a sandwich irmnunoassay using antibodies. An antibody is a protein produced by the immune system of an animal in response to a foreign molecule, which is called an antigen. An antibody specifically recognizes and binds to the antigen that stimulated its synthesis. [Pg.344]

Hence zeolite synthesis shares some of the same combinatorial self organization and self learning aspects as seen in the antibody system. During zeolite crystallization template molecules are incorporated in unique positions. Molecular mechanics techniques have been developed ] that allow the prediction of optimum template zeohte interaction useful to select template molecules to synthesize preselected zeohte structmes. [Pg.355]

We have thus far explored the possibilities that the impairment of antibody production in the vitamin deficiencies might be linked either to a faulty processing of the antigen or to a disturbance in the integrity of the antibody-synthesizing cells. There is also the distinct likelihood that the vitamins, by virtue of their close interrelationships with various enzyme systems, function directly in the enzymatic reactions involved in antibody synthesis. Our complete ignorance of these reactions constitutes an effective barrier against any attempt to implicate the vitamins in specific enzymatic mechanisms. However, certain points of interest are worthy of discussion. [Pg.18]

Cytokines. Figure 1 Inhibition of cytokine synthesis during activation of the specific immune system. The monoclonal antibodies Muromonab and Basiliximab are specific for the CD3 complex of the T-cell receptor, and for the IL-2 receptor on lymphocytes, respectively. Cyclosporin and Tacrolimus inhibit activation of cytoplasmic NF-AT, a transcription factor essential for activation of the IL-2 gene ( NFAT Family of Transcription Factors). Sirolimus interferes with mTOR signaling and inhibits IL-2 dependent proliferation. Red pharmaka, blue target proteins. [Pg.412]


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Antibodies synthesis

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