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Antibodies characteristics

Table 1 shows a list of antibody characteristics utilized for their separation from crude mixtures. [Pg.546]

Vincent A, Newsom-Davis J. Acetylcholine receptor antibody characteristic in myasthenia gravis. Patients with penicillamine-induced myasthenia or idiopathic myasthenia of recent onset. Clin Exp Immunol 1982 49 266-272. [Pg.476]

However, in the long term, ELISA is an ephemeral format. Even when streamlined and automated, it has too many steps. Certainly we should realize that it will be replaced by other systems, the most exciting of which will be biosensors. Also, other formats offer a proprietary edge in the market place which will be very important in the maturation of immunoassay systems in the environmental field. Finally, different formats will lend themselves to different environmental problems. We should continually emphasize that the same reagents can be used in many formats. Possibly in small letters we also should caution that certain antibody characteristics may be more important in one format than another, that some formats are more resistant to matrix effects, and that relative cross reactivities of compounds can change as one changes the subtle principles upon which an immunoassay works. For this reason a clear choice of formats should be made before initiating validation studies. [Pg.118]

The antigens induce not only an immune response but equally react with the antibodies, which are caused to appear by the living organism. However, these two properties are different. Small organic molecules such as pesticides are not able of inducing a production of antibodies. In the other hand, the antigens will react if an adapted antibody is already present these small molecules are called the haptens. To generate the antibodies characteristic to a hapten, the latter must be attached by a covalent bond to transporter proteins (BSA or HSA bovine or human serum albumin), or to a polysaccharide. Therefore, the hapten must have reactive functionality and this structural modification must not influence the specificity of the antibodies that will be produced. [Pg.426]

Affinity and Avidity Antibody strength of binding and specificity are the main determinants of the sensitivity and ruggedness of any immunoassay. Strength of binding reflects both affinity and avidity, which are described in more detail below and summarized in Table 3.3. Understanding these antibody characteristics will help in the appropriate selection of antibodies for assay development. A variety of methods for determining the affinity constant [13] and avidity index [14,15] have been reported. [Pg.48]

Antibodies are produced in animals after stimulation of the immune system by injecting the target molecule in a procedure called immunization. It is necessary to highlight that the production of antibodies is initiated in an in vivo system and the outcome (i.e., antibody features) is subjected to the specific response of each animal treated. In other words, antibody characteristics cannot be fully predetermined, due to variation in the response of each immunized individual. However, the quality of antibodies, which is critical to provide a good immunoassay, can be optimized, although not controlled completely, for the reasons mentioned above. [Pg.224]

The most used EIA reagents conjugate a fluotophote such as fluorescein-isothiocyanate (EITC) or thodarnine—isothiocyanate to antibody (or antigen) free amino groups. Examples of other commonly used fluotophotes for EIA and their spectral characteristics ate presented in Table 3. EIA assays ate available in sandwich and competitive formats similar to EIAs. Unlike EIA kits which can be used directly with visual color deterrnination, EIAs require a fluorometer, and thus ate primarily laboratory-based. [Pg.26]

Biosensors ai e widely used to the detection of hazardous contaminants in foodstuffs, soil and fresh waters. Due to high sensitivity, simple design, low cost and real-time measurement mode biosensors ai e considered as an alternative to conventional analytical techniques, e.g. GC or HPLC. Although the sensitivity and selectivity of contaminant detection is mainly determined by a biological component, i.e. enzyme or antibodies, the biosensor performance can be efficiently controlled by the optimization of its assembly and working conditions. In this report, the prospects to the improvement of pesticide detection with cholinesterase sensors based on modified screen-printed electrodes are summarized. The following opportunities for the controlled improvement of analytical characteristics of anticholinesterase pesticides ai e discussed ... [Pg.295]

It was established that Ab to Klebsiella pneumoniae didn t demonstrate the cross-reactivity to antigens of the relative bacterial species so, it could be considered that antibodies investigated was highly specific only to the own antigen. The physical-chemical characteristics of the immunological interaction such as constants of formation of Ag-Ab complex were obtained. The binding constants of immune complex were Ka =(9.7 l.l)-10 and Ka,=(1.7+0.3)T0 (mg/ml)f... [Pg.329]

Fermentation broths are complex, aqueous mixtures of cells, comprising soluble extracellular, intracellular products and any unconverted substrate or unconvertible components. Recovery and extraction of product is important in bioprocess engineering. In particular separation is a useful technique it depends on product, its solubility, size of the process, and product value. Purification of high-value pharmaceutical products using chromatography such as hormones, antibody and enzymes is expensive and difficult to scale up.1 Tire necessary steps to follow a specific process depend on the nature of the product and the characteristics of the fermentation broth. There are a few steps for product recovery the following processes are discussed, which are considered as an alternative for product recovery from fermentation broth. [Pg.170]

The behavior of liposomes in vivo can be influenced to a considerable extent by varying chemical composition and physical properties. Parameters affecting rate of clearance from the blood and tissue distribution include size, composition, dose, and surface characteristics (e.g., charge, hydrophobicity, presence of homing devices such as antibodies). [Pg.281]

Mastocytosis is recognized in most patients because of the presence of characteristic cutaneous lesions [10]. A positive Darier s sign and/or histological examination of the skin using metachromatic stains, or by immunohistochemistry using antibodies to mast cell tryptase, helps confirm the diagnosis of cutaneous disease. [Pg.118]

Other sensor applications can be considered if some sensitive biological molecules (such as antibodies or receptors) are attached to the nanogranule. If, for example, an antibody molecule is attached to it, then the granule is placed between two electrodes, and single-electron current flows between them. The step value of the coulomb staircase depends on the capacity of the junctions. When the antibody molecule binds specific antigen, the capacity value will be changed, and, therefore, the step value of the VH characteristics will also change. [Pg.185]

It is interesting that the stimulus compounds used in the study differ widely in their molecular structures, and yet they all interact with antibodies to thaumatin. It is, therefore, probable that a single receptor-structure responds to all sweet stimuli,there being a variation in the relative effectiveness of sweet stimuli across individual nerve-fibers, and the characteristics of all receptor sites do not appear to be identical. Earlier elec-trophysiological studies of single primary, afferent taste-neurons uniformly agreed that individual fibers very often have multiple sensitivities, and that individual, gustatory receptors are part of the receptive field of more than one afferent fiber. " We have yet to learn how these interact, and the nature of their excitatory, or possible inhibitory, relations, or both. [Pg.334]

A novel antibody supramolecule is designed and prepared by using immunoglobulin M (IgM) as a core and chemically modified IgGs as branches as shown in Scheme 3. The characteristic binding ability and specificity of IgG were found to remain during the chemical modification of IgG with 3MPylC. When IgM for... [Pg.249]

While much care has to be used in performing competitive protein binding assays, most well-equipped and staffed clinical laboratories should have no serious problem in undertaking such assays. The biggest problem that may be encountered is the selection of a dependable and reliable manufacturer for reagents. Problems that may arise are non-purity of standards and label non-specificity of antibodies or the inability to maintain any of these characteristics from lot to lot. It therefore is a good practice to evaulate a few manufacturers before selecting one for routine use. [Pg.67]

Idiotypic network. Idiotypic determinants (idiotypes) are unique antigenic epitopes characteristic of the antigen receptors on the surface of T and B cells. They are associated with the variable regions of these receptors. Antibodies produced by B cells as the result of antigenic stimulation can themselves stimulate the production of auto-anti-idiotypic antibodies which have the ability to combine with the B-cell receptor (Ig) and thus can dampen down the immune response. Idiotypes may likewise stimulate the production of T cells specific for idiotypic determinants. Jerne (1974) postulated his... [Pg.296]


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