نتایج جستجو برای: elisa igm

تعداد نتایج: 61040  

2011
Jie Cao Qiuli Chen Huaqun Zhang Peipei Qi Chao Liu Xufang Yang Niansong Wang Baohua Qian Jinhong Wang Shaohua Jiang Hua Yang Shuhan Sun Wei Pan

Detection of specific antibodies against hepatitis C virus (HCV) is the most widely available test for viral diagnosis and monitoring of HCV infections. However, narrowing the serologic window of anti-HCV detection by enhancing anti-HCV IgM detection has remained to be a problem. Herein, we used LD5, a novel evolved immunoglobulin-binding molecule (NEIBM) with a high affinity for IgM, to develo...

Journal: :acta medica iranica 0
mehrdad hasibi department of infectious diseases, amir alam hospital, tehran university of medical sciences, tehran, iran. sirus jafari department of infectious diseases, imam khomeini hospital, tehran university of medical sciences, tehran, iran. habibollah mortazavi department of infectious diseases, imam khomeini hospital, tehran university of medical sciences, tehran, iran. marjan asadollahi department of neurology, loghman hospital, shahid beheshti university of medical sciences, tehran, iran. gholamreza esmaeeli djavid department of infectious diseases, imam khomeini hospital, tehran university of medical sciences, tehran, iran.

in endemic area the most challenging problem for brucellosis is to find a reliable diagnostic method. in this case-control study, we investigated the accuracy of elisa test for diagnosis of human brucellosis and determined the optimal cut-off value for elisa results in iran. the laboratory diagnosis of brucellosis was performed by blood isolation of brucella organism with a bactec 9240 system a...

Journal: :Japanese journal of infectious diseases 2008
Gulcin Cakan Fatma Betul Bezirci Askin Kacka Salih Cesur Sebahat Aksaray Deniz Tezeren Dilek Saka Kamruddin Ahmed

This study was performed to evaluate commercial brucella immunoglobulin G and M enzyme-linked immunosorbent assay (IgG and IgM ELISA) kits for the diagnosis of human brucellosis and to suggest a candidate prognostic marker for human brucellosis. We determined the serum levels of brucella IgG, IgM, C-reactive protein (CRP), soluble CD14 (sCD14), and neopterin in patients with brucellosis and com...

Journal: :Journal of clinical microbiology 1998
A J Cuzzubbo D W Vaughn A Nisalak S Suntayakorn J Aaskov P L Devine

Saliva was collected prospectively from patients presenting with suspected dengue infection 4 to 8 days after the onset of symptoms and assayed by a commercial dengue immunoglobulin M (IgM) and IgG capture enzyme-linked immunosorbent assay (ELISA) (PanBio Dengue Duo ELISA). Laboratory diagnosis was based on virus isolation and on hemagglutination inhibition (HAI) assay and an in-house IgM and I...

Journal: :Indian Journal of Medical Microbiology 2019

Journal: :Journal of clinical microbiology 1999
J P Brinker N R Blacklow X Jiang M K Estes C L Moe J E Herrmann

Sera obtained from adult volunteers inoculated with genogroup II Norwalk-like viruses (NLVs), Hawaii virus, and Snow Mountain virus and from patients involved in outbreaks of gastroenteritis were tested for genogroup II NLV Mexico virus-specific immunoglobulin M (IgM) by use of a monoclonal antibody, recombinant Mexico virus antigen (rMXV)-based IgM capture enzyme-linked immunosorbent assay (EL...

2005
W. Lüke T. Weber

Objectives: Progressive multifocal leukoencephalopathy (PML) is caused by a reactivated infection with the human polyomavirus JC (JCV). Primary infection with JCV has not been linked to any disease in humans. Using recombinant viral protein 1 (VP1) of JCV as antigen, we developed an enzyme linked immunosorbent assay (ELISA) for the detection of VP1-speciŽc IgM. Methods: Two different direct ELI...

2011
Karl Egerer Dirk Roggenbuck Thomas Büttner Barbara Lehmann Annushka Kohn Philipp von Landenberg Rico Hiemann Eugen Feist Gerd-Rüdiger Burmester Thomas Dörner

INTRODUCTION Diagnosis of antiphospholipid syndrome (APS) still remains a laboratory challenge due to the great diversity of antiphospholipid antibodies (aPL) and their significance regarding APS-diagnostic criteria. METHODS A multi-line dot assay (MLDA) employing phosphatidylserine (PS), phosphatidylinositol (PI), cardiolipin (CL), and beta2-glycoprotein I (β2 GPI) was used to detect aPL, im...

Journal: :The Journal of infectious diseases 1996
B J Johnson K E Robbins R E Bailey B L Cao S L Sviat R B Craven L W Mayer D T Dennis

An ELISA containing a purified flagellar antigen from Borrelia burgdorferi (FLA-ELISA) was evaluated. The FLA-ELISA, detecting IgM and IgG together, did not have adequate specificity by itself. Good accuracy was obtained, however, when the FLA-ELISA was the first step in a two-step protocol that used immunoblotting as a conditional second test. Samples that scored positive or equivocal by the F...

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