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Direct Competitive Enzyme-Linked Immunosorbent Assay (ELISA).
Cold Spring Harbor Protocols, 2017The competitive enzyme-linked immunosorbent assay (ELISA) (cELISA; also called an inhibition ELISA) is designed so that purified antigen competes with antigen in the test sample for binding to an antibody that has been immobilized in microtiter plate ...
T. Kohl, C. Ascoli
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ELISA: Enzyme-Linked Immunosorbent Assay
Hospital Practice, 1978Similar in design to radioimmunoassay, comparable in sensitivity and specificity but easier, safer, and less expensive, this new diagnostic technique uses enzyme-labeled rather than isotope-labeled reagents. The end point is a color change that can be assessed by colorimetry or with the naked eye.
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American Journal of Tropical Medicine and Hygiene, 1989
The diagnostic sensitivity and specificity of detection of anti-dengue IgM by antibody capture enzyme-linked immunosorbent assay (ELISA) was investigated in dengue infections in a variety of clinical settings. Sera from uninfected controls were uniformly
B. Innis+7 more
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The diagnostic sensitivity and specificity of detection of anti-dengue IgM by antibody capture enzyme-linked immunosorbent assay (ELISA) was investigated in dengue infections in a variety of clinical settings. Sera from uninfected controls were uniformly
B. Innis+7 more
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Enzyme linked immunosorbent assay (ELISA) for paraquat
International Journal of Immunopharmacology, 1983An Enzyme Linked Immunosorbent Assay (ELISA) has been developed for the estimation of paraquat. The amount of paraquat present in samples of human plasma was estimated in terms of the degree to which it combined with a rabbit antibody raised to a conjugate to paraquat with bovine serum albumin.
S.T. Walsh, G.E. Davies, Z. Niewola
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An enzyme‐linked immunosorbent assay for phytochrome
Physiologia Plantarum, 1984A double‐antibody sandwich, enzyme‐linked immunosorbent assay has been developed for phytochrome in Avena sativa L. cv. Saladin. An immunoglobulin fraction of rabbit antiserum raised to 118 kdalton phytochrome was used with alkaline phosphatase as the enzyme label.
Brian Thomas+2 more
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Analytical Chemistry, 2015
Lowering the detection limit is critical to the design of bioassays required for medical diagnostics, environmental monitoring, and food safety regulations.
Jiajie Liang+8 more
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Lowering the detection limit is critical to the design of bioassays required for medical diagnostics, environmental monitoring, and food safety regulations.
Jiajie Liang+8 more
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Development of an enzyme-linked immunosorbent assay for toosendanin
Analytica Chimica Acta, 2008Enzyme-linked immunosorbent assays (ELISAs) were developed by using polyclonal antibody for toosendanin (TSN), a biopesticide from Melai toosendan Sieb. et Zucc. Their application in the determination of this analyte in spiked cabbage, tomato and apple samples was studied.
Jing Zhang+7 more
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Enzyme-Linked Immunosorbent Assay: Types and Applications.
Methods in molecular biology, 2023H. Hayrapetyan+3 more
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In Analysis, 2014
The detection limit is one of the most important performance parameters for bioanalytical techniques. Here we present a generic method to estimate the detection limit of biomolecular assays based on a step-by-step analysis of the assay procedure.
Shiyun Zhang+3 more
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The detection limit is one of the most important performance parameters for bioanalytical techniques. Here we present a generic method to estimate the detection limit of biomolecular assays based on a step-by-step analysis of the assay procedure.
Shiyun Zhang+3 more
semanticscholar +1 more source
Thermometric enzyme linked immunosorbent assay: TELISA
Biochimica et Biophysica Acta (BBA) - Enzymology, 1977A new method, thermometric enzyme linked immunosorbent assay (TELISA), for the assay of endogenous and exogenous compounds in biological fluids is described. It is based on the previously described enzyme linked immunosorbent assay technique, ELISA, but utilizes enzymic heat formation which is measured in an enzyme thermistor unit.
Bo Sanfridson+3 more
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