๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Use of enzyme-linked immunosorbent assay for the diagnosis of equineHistoplasmosis farciminosi(epizootic lymphangitis)

โœ Scribed by M. A. Gabal; K. A. Mohammed


Publisher
Springer Netherlands
Year
1985
Tongue
English
Weight
217 KB
Volume
91
Category
Article
ISSN
0301-486X

No coin nor oath required. For personal study only.

โœฆ Synopsis


An enzyme-linked immunosorbent assay was evaluated for the detection of antibody in sera of equine naturally infected with Histoplasmafarciminosum 'epizootic lymphangitis'. Ten sera from naturally infected horses were tested. A hydrogen peroxide ABTS mixture constituted the substrate. The reactions were read as the absorbance values measured at 405 nm using a spectrophotometer. The standard deviation and the average percentage of the absorbance values of the different serum samples were considered in the interpretation of the results. All sera were proved positive with variations in the different samples. Ground preparation of four weeks old growth of the fungus in a phosphate buffer saline was used as antigen. A peroxidase labeled goat anti-equine IgG was used as a conjugate.


๐Ÿ“œ SIMILAR VOLUMES


Enzyme-Linked immunosorbent assay of cor
โœ Dr. J. Donald Coonrod; Paraskevi Karathanasis; Robert F. Betts; James C. Donofri ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 716 KB

A solid-phase enzyme-linked immunosorbent assay (ELISA) with monoclonal secondary antibodies was used to detect matrix protein and nucleoprotein of influenza A. The sensitivity of the ELISA for highly purified A/Brazil nucleoprotein and matrix protein was 0.05 and 1.0 ng, respectively. Nasal washes

Diagnosis of human coronavirus infection
โœ Malcolm R. Macnaughton; Dianne Flowers; David Lsaacs ๐Ÿ“‚ Article ๐Ÿ“… 1983 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 445 KB

An enzyme-linked immunosorbent assay (ELISA) was developed for diagnosing human coronavirus (HCV) infections in children. One hundred and seventy seven nose swabs, throat swabs, and nasopharyngeal aspirates were collected from 30 children suffering from acute respiratory infections. These samples we