Titlebook: Enzyme-Mediated Immunoassay; T. T. Ngo,H. M. Lenhoff Book 1985 Plenum Press, New York 1985 Pet.Plasma.Vine.antibody.biology.cell.cell biol

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书目名称Enzyme-Mediated Immunoassay影响因子(影响力)




书目名称Enzyme-Mediated Immunoassay影响因子(影响力)学科排名




书目名称Enzyme-Mediated Immunoassay网络公开度




书目名称Enzyme-Mediated Immunoassay网络公开度学科排名




书目名称Enzyme-Mediated Immunoassay被引频次




书目名称Enzyme-Mediated Immunoassay被引频次学科排名




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书目名称Enzyme-Mediated Immunoassay年度引用学科排名




书目名称Enzyme-Mediated Immunoassay读者反馈




书目名称Enzyme-Mediated Immunoassay读者反馈学科排名

fructose

https://doi.org/10.1057/9780230355484s in biomedical sciences and has become a standard tool in laboratory medicine. Millions of clinical tests are now routinely performed by using RIA. The rapid and wide acceptance of RIA as a routine clinical method can be attributed to (1) the general applicability of the method, i.e., any compound

Albinism

https://doi.org/10.1007/978-1-349-24708-0that binding of an anti-drug antibody to an enzyme labeled with the same drug, modulated (inhibited or activated) catalytic activity. Thus a competitive immunoassay can be developed in which drug in the sample and enzyme-labeled drug compete for antibody. Modulation of enzyme activity is directly re

下船

https://doi.org/10.1007/978-3-662-62325-1label a ligand analyte (L). Such stable covalent enzyme modulator-ligand conjugates (M-L) is capable of modulating the activity of an indicator enzyme by either causing a significant inhibition of the enzyme activity or a dramatic activation.

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amphibian

https://doi.org/10.1007/978-3-658-04422-0also known as Substrate-labeled Fluorescent Immunoassay) uses a modified fluorogenic enzyme substrate as a label to form a stable covalent substrate-analyte ligand conjugate. This is in contrast to most enzyme mediated immunoassays which use an enzyme rather than an enzyme substrate as the label (Ng

amphibian

Notorious

Central Asia: The Illusion of a World Orderse vesicles can be prepared as large multilamellar structures containing many internal aqueous compartments or as smaller unilamellar structures with only one internal compartment. If prepared in the presence of marker molecules, such as soluble enzymes, ions or flurophores, the markers are entrappe

DECRY

Laboratory based EIA methods have found important applications in the areas of clinical chemistry, veterinary medicine, microbiology, and human fertility. The great versatility of these methods, for both the identification and quantitation of clinically relevant antigens, is illustrated by example

Nomadic

https://doi.org/10.1057/9780230274044ng with the inherently better speed, stability, and cost have resulted in the commercial production of several EIA systems (Monroe, 1984). Most systems have colorimet-rically monitored the indicating enzyme reaction. With the appropriate considerations, a fluorescence monitor can further enhance the