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Antibodies antibody activity

Host-derived (e.g., antigen-antibody complexes, activated complement fragments, inflammatory bile acids, urate crystals, certain androgenic steroid metabolites [e.g., etiocholanolone], certain lymphocyte products)... [Pg.501]

Chatenoud L (2003) CD3-specific antibody-induced active tolerance from bench to bedside. Nat. Rev. Immunol 3 123-132... [Pg.1181]

Active and passive immunity involve tiie use of agents that stimulate antibody formation (active immunity) or tiie injection of ready-made antibodies found in tiie serum of immune individuals or animals (passive immunity). The following sections describe active and passive immunity. [Pg.568]

Zimarino, V, Wilson, S., Wu, C. (1990b). Antibody mediated activation of Drosophila heat shock factor in vitro. Science 249, 546-549. [Pg.462]

Like many other antibodies, the activity of antibody 14D9 is sufficient for preparative application, yet it remains modest when compared to that of enzymes. The protein is relatively difficult to produce, although a recombinant format as a fusion vdth the NusA protein was found to provide the antibody in soluble form with good activity [20]. It should be mentioned that aldolase catalytic antibodies operating by an enamine mechanism, obtained by the principle of reactive immunization mentioned above [15], represent another example of enantioselective antibodies, which have proven to be preparatively useful in organic synthesis [21]. One such aldolase antibody, antibody 38C2, is commercially available and provides a useful alternative to natural aldolases to prepare a variety of enantiomerically pure aldol products, which are otherwise difficult to prepare, allovdng applications in natural product synthesis [22]. [Pg.68]

Cocaine vaccine Passive monoclonal antibodies, active vaccinations Further studies are required for this novel approach. [Pg.196]

Immunoglobulins are associated with the y-globulin fraction of plasma proteins but, as stated earlier, not all immunoglobulins exhibit antibody activity. [Pg.285]

Figure 20.9 Polysaccharide groups on antibody molecules may be oxidized with periodate to create aldehydes. Modification with biotin-hydrazide results in hydrazone linkages. The sites of modification using this technique often are away from the antibody-antigen binding regions, thus preserving antibody activity. Figure 20.9 Polysaccharide groups on antibody molecules may be oxidized with periodate to create aldehydes. Modification with biotin-hydrazide results in hydrazone linkages. The sites of modification using this technique often are away from the antibody-antigen binding regions, thus preserving antibody activity.
Freedman, M.H., Grossberg, A.L., and Pressman, D. (1968) The effects of complete modification of amino groups on the antibody activity of antihapten antibodies. Reversible inactivation with maleic anhydride. Biochemistry 7, 1941-1950. [Pg.1064]

Antibodies that, by binding to the cell surface antigen, mark the tumour cell for destruction. NK cells and macrophages express cell surface receptors that bind to the antibody Fc region (Box 13.2). Thus, antibody bound to tumour antigens directs these immune elements directly to tumour surface. Antibodies also activate complement, which is capable of directly lysing tumour cells. [Pg.382]

No antibody activity was found after oral immunization in any of the individual rabbits immunized with liposphere R32NS 1-vaccine formulation. However, rabbit immunization by all parenteral routes tested resulted in enhanced immunogenicity, with increased antibody IgG levels over the entire postimmunization period. The individual rabbit immune response shows that immunization by subcutaneous injection was the most effective vaccination route among all parenteral routes of administration tested. [Pg.8]

The feasibility of polymeric biodegradable lipospheres as carriers for the controlled release of a recombinant malaria antigen was also demonstrated. Polymeric lipospheres containing R32NS1 malaria antigen were able to induce very high levels of antibody activity after a single injection, in the absence of immunomodulators. [Pg.11]

Defining the biochemical mechanisms that couple stimulation at the cell surface to secretion by exocytosis is a major focus in biological research. In the mast cell, the steps by which immunologic secretagogues (for example, specific antigen, anti-IgE antibodies) activate a secretory response have been extensively studied and there are several reviews covering this area [ 12-14, 16, 121, 177],... [Pg.176]

Antibodies are members of a group of proteins known collectively as immunoglobulins. The name is derived from the observation that during electrophoresis of blood plasma the proteins associated with antibody activity migrate with the gamma globulin fraction. [Pg.231]

While the presentation thus far has emphasized the programmed relationship of hapten design and consequent antibody catalytic activity, there is a growing number of examples where the detailed examination of catalysis reveals mechanistic features that were not evidently design features of the system at the outset. Such discoveries are clearly a strength rather than a weakness of... [Pg.276]

Binding of nitroso-procainamide to histone proteins may perturb chromatin structure or catabolism, resulting in immunogenic forms of DNA-free histones. In fact, all sera of patients (n = 24) with procainamide-induced Lupus showed IgG and IgM antibody activity against various histone components of chromatin (chromosome subunits)122. The nature of the procainamide adduct to histone proteins still awaits elucidation. [Pg.1023]

In summary, these three approvals with the noncytotoxic monoclonal antibodies demonstrated activity based on survival (Avastin), TIP in an enriched population (Avastin in renal cell cancer), a pure response with endpoint (Campath), and a clever response rate to a combination vs. a reference point response rate with that new agent alone (Cetuximab). [Pg.451]


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