By B. Salomons, J. Sigmond, M. Terpstra
This e-book offers the result of a finished examine of literature on patents, patent purposes and different literature, resembling magazine articles. The survey covers literature released from the us, Japan and Western Europe among January 1980 and April 1991.
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Extra resources for Immunoassay: A survey of patents, patent applications and other literature 1980-1991
As the method to bind an amino group and a carboxyl group, the peptidebinding method of carboxyl group to succinimido ester, the carbodiimide method, the Woodward reagent method are known. The periodate oxidation method (Nakane method) where a bridge between amino group and sugar chain forms is also utilized. In the case of using a thiol group, for example, a carboxyl group is first converted to a succinimido ester, and this ester group is then allowed to react with cysteine to introduce the thiol group, and both thiol groups are bound by using a thiol-reactive bifunctional cross-linking reagent NON-ANTIGEN SPECIFIC METHODS, APPARATUS AND KITS FOR IMMUNOASSAY 37 such as phenylene-bismaleimide.
T. and CANOVA-DAVIS, (94)), prepared a liposome assay reagent for determination of an analyte in a homogeneous immunoassay. The reagent includes a suspension of oligolamellar lipid vesicles containing encapsulated glucose-6-phosphate dehydrogenase (G6PD), at a specific activity of between about 1–10 units mu-mole vesicle vesicle lipid, and glucose6-phosphate (G6P) at a concentration of at least about 5 mM. The next figure shows a graphic representation of turbidity against time for several antigen/antibody reaction.
An enzymatic substrate, an enzyme inhibitor, a prosthetic group of an enzyme, a coenzyme, or an enzyme itself, or a fragment thereof. P. 4)). The bound fraction activates the first component of complement whereby a substrate present in the fluid is modulated to provide a detectable signal. The signal may be detected to establish the presence or absence of the analyte in the fluid, or it may be quantitatively measured to determine the concentration of the analyte in the fluid. Because the enzyme is added to the assay medium in an inactive form and is activated only by antibody bound to antigen, unbound antibody does not activate the enzyme and does not interfere with signal generation induced by bound antibody.
Immunoassay: A survey of patents, patent applications and other literature 1980-1991 by B. Salomons, J. Sigmond, M. Terpstra