|Statement||by Jeffrey C. Travis.|
|The Physical Object|
|Number of Pages||168|
Author(s): Travis,Jeffrey C Title(s): Fundamentals of RIA and other ligand assays: a programmed text/ by Jeffrey C. Travis. Country of Publication: United States Publisher: Anaheim, Calif.: Radioassay Publishers, c ELISA is the most widely used ligand binding assay platform within and outside the pharmaceutical industry. Formats include direct, indirect and sandwich assays which are often used as a basis for comparison with novel platforms in development and are run manually or semi-automated on 96 well plates where samples are measured in by: In book: Ligand-Binding Assays: Development, Validation, and Implementation in the Drug Development Arena, pp - Cite this publication Huifen F. Wang Ph.D. Travis JC () Fundamentals of RIA and other ligand assays. Scientific Newsletters, Anaheim Google Scholar Van Dyke K () Biolumisencence and chemiluminescence: instruments and applications, vol .
FUNDAMENTALS OF RIA AND OTHER LIGAND ASSAYS Jeffrey C. Travis, Radioassay Publishers, Anaheim, , pp, $ This soft-bound booklet (5Y2 X 8Y2 in.) is designed to teach the basic principles and the practical applications of ligand binding assays. Referred to as "a programmed. A 'read' is counted each time someone views a publication summary (such as the title, abstract, and list of authors), clicks on a figure, or views or downloads the full-text. Enzymes represent one. Immunoassay, DNA Analysis, and Other Ligand Binding Assay Techniques: From Electropherograms to Multiplexed, Ultrasensitive Microarrays on a Chip Roger P. Ekins Journal of Chemical Education , 76, 6, (Article). Radioimmunoassay (RIA) is a highly sensitive way to measure the concentration of antigen in a sample. In this assay, a quantity of the antigen of interest is tagged with a radioactive isotope (typically of iodine or iodine) and mixed with a known amount of its cognate antibody.
ELISA (enzyme-linked immunosorbent assay) is a plate-based assay technique designed for detecting and quantifying peptides, proteins, antibodies and hormones. In an ELISA, an antigen must be immobilized to a solid surface and then complexed with an antibody that is linked to an enzyme. Detection is accomplished by assessing the conjugated enzyme activity via incubation with a . The basic enzyme-linked immunosorbent assay (ELISA), or enzyme immunoassay (EIA), is distinguished from other antibody-based assays because separation of specific and non-specific interactions occurs via serial binding to a solid surface, usually a polystyrene multiwell plate, and because quantitative results can be achieved. These assays, in general, use labeled antigens, haptens, or antibody for recognizing the target analytes. Furthermore, different variants of immunoassays have been reported since the onset of such powerful efficient emerging technique, including radioimmunoassay (RIA), enzyme immunoassays (EIA), by: 4. Bibliographic record and links to related information available from the Library of Congress catalog.. Note: Contents data are machine generated based on pre-publication provided by the publisher. Contents may have variations from the printed book or be incomplete or contain other coding.