نتایج جستجو برای: igm capture eia

تعداد نتایج: 140145  

Journal: :The American journal of tropical medicine and hygiene 2008
Stephanie S Groves Michael J Turell Charles L Bailey Victor N Morozov

To reduce the assay time for detecting virus-specific antibodies in serum, we developed microarray-based active immunoassay techniques for detecting West Nile virus (WNV)-specific IgM molecules in chicken blood. The assay uses electrophoretic concentration of IgM molecules onto WNV antigens arrayed on a dialysis membrane followed by detection of bound IgM molecules with functionalized magnetic ...

Journal: :Journal of clinical pathology 1984
S F Pugh

IgM antibody capture radioimmunoassays were developed to detect coxsackie virus B1-B5 specific IgM. Specific IgM was detected in sera from all patients with coxsackie B virus infections proved by isolation; however, sera from 13/32 patients with rising neutralising antibody titres were negative in the assay. Frequent heterotypic responses were seen among the positive sera. Thirty seven patients...

Journal: :Journal of clinical microbiology 2000
K H Engler A Efstratiou

A rapid enzyme immunoassay (EIA) was developed for the phenotypic detection of diphtheria toxin among clinical isolates of corynebacteria. The assay uses equine polyclonal antitoxin as the capture antibody and an alkaline phosphatase-labeled monoclonal antibody, specific for fragment A of the toxin molecule, as the detecting antibody. The assay is rapid, sensitive, and specific: a final result ...

Journal: :Journal of clinical microbiology 2008
Wenlan Zhang Martina Bielaszewska Matthias Pulz Karsten Becker Alexander W Friedrich Helge Karch Thorsten Kuczius

Shiga toxin (Stx)-producing Escherichia coli (STEC) strains secrete toxins that are major virulence factors and diagnostic targets, but some STEC strains secrete Stx in amounts that cannot be detected using conventional cell cytotoxicity or immunological assays. Therefore, there is an urgent need for more-sensitive Stx detection methods. We describe the development of an assay that can detect l...

Journal: :Journal of clinical microbiology 1994
S C Arya

The ,-capture assay to measure poliovirus-specific immunoglobulin M (IgM) antibodies for three poliovirus serotypes in serum and cerebrospinal fluid (CSF) in 114 patients with clinically determined acute poliomyelitis at Karachi, Pakistan, employed 35S-methionine-radiolabelled polioviruses. In the microwell format, the appearance of poliovirus-specific IgM antibodies appeared a sensitive and sp...

Journal: :Journal of clinical microbiology 1983
B Forghani C K Myoraku N J Schmidt

Monoclonal antibodies to human immunoglobulin M (IgM) were used in a four-phase enzyme immunofluorescence "capture" assay for determination of IgM antibodies to measles and rubella viruses. Little or no background reactivity was seen in the test system, and interfering effects of rheumatoid factor were avoided by preabsorption of test sera with aggregated human IgG. Virus-specific IgM antibody ...

Journal: :Clinical and vaccine immunology : CVI 2012
Stuart D Blacksell Richard G Jarman Robert V Gibbons Ampai Tanganuchitcharnchai Mammen P Mammen Ananda Nisalak Siripen Kalayanarooj Mark S Bailey Ranjan Premaratna H Janaka de Silva Nicholas P J Day David G Lalloo

Seven commercial assays were evaluated to determine their suitability for the diagnosis of acute dengue infection: (i) the Panbio dengue virus Pan-E NS1 early enzyme-linked immunosorbent assay (ELISA), second generation (Alere, Australia); (ii) the Panbio dengue virus IgM capture ELISA (Alere, Australia); (iii) the Panbio dengue virus IgG capture ELISA (Alere, Australia); (iv) the Standard Diag...

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