نتایج جستجو برای: dot immunogold filtration assay

تعداد نتایج: 287086  

2017
Po-Chiung Fang Chun-Chih Chien Hun-Ju Yu Ren-Wen Ho Shin-Ling Tseng Yu-Hsuan Lai Ming-Tse Kuo

PURPOSE To evaluate a bacterial dot hybridization (BDH) assay for the diagnosis of bacterial keratitis (BK). METHODS Sixty-one qualified corneal scrapings from 61 patients with suspected microbial keratitis were collected consecutively and prospectively. Among the 61 patients, 16 cases were BK and 45 cases were non-BK, including fungal keratitis, viral keratitis, parasitic keratitis, and non-...

Journal: :Journal of clinical microbiology 1990
M Musiani M Zerbini G Gentilomi G Gallinella S Venturoli D Gibellini M La Placa

A dot blot hybridization immunoenzymatic assay for the rapid detection of cytomegalovirus DNA in urine samples was developed by using a digoxigenin-labeled probe which was immunoenzymatically visualized by antidigoxigenin Fab fragments labeled with alkaline phosphatase. A total of 516 urine samples from different groups of subjects were analyzed, and the hybridization assay was able to yield re...

2014
Seon-Ju Yeo Dinh Thi Huong Nguyen Ngoc Hong Chun-Ying Li Kyunghan Choi Kyoungsik Yu Du-Young Choi Chom-Kyu Chong Hak Soo Choi Shyam Kumar Mallik Hak Sung Kim Haan Woo Sung Hyun Park

Great efforts have been made to develop robust signal-generating fluorescence materials which will help in improving the rapid diagnostic test (RDT) in terms of sensitivity and quantification. In this study, we developed coumarin-derived dendrimer-based fluorescent immunochromatographic strip test (FICT) assay with enhanced sensitivity as a quantitative diagnostic tool in typical RDT environmen...

Journal: :Chemical communications 2015
Guichi Zhu Kun Yang Chun-Yang Zhang

Telomerase is a promising biomarker and a therapeutic target due to its extensive expression in human tumors such as lung cancer and breast cancer. Here, we develop a single quantum dot (QD)-based biosensor for the sensitive detection of telomerase activity. This single QD-based biosensor has significant advantages of simplicity and high sensitivity, and it can be applied for the discrimination...

Journal: :Journal of clinical microbiology 1996
T Belay R Cherniak E B O'Neill T R Kozel

A method is described for the serotyping of Cryptococcus neoformans based on direct analysis of culture supernatants for the major type-specific capsular antigen, glucuronoxylomannan. Factor sera prepared by absorption of polyclonal rabbit antisera (Iatron Laboratories, Inc., Tokyo, Japan) or selected anti-C. neoformans monoclonal antibodies were used in a dot enzyme assay to detect the presenc...

Journal: :Journal of clinical microbiology 1989
J Flores K Y Green D Garcia J Sears I Perez-Schael L F Avendaño W B Rodriguez K Taniguchi S Urasawa A Z Kapikian

We have developed a hybridization assay that permits distinction of rotavirus serotypes 1, 2, 3, and 4. The serotype of rotaviruses from stool samples or tissue culture was recognized by hybridization of specific probes to (i) blots of viral double-stranded RNAs electrophoresed in agarose gels (Northern blots) or (ii) heat-denatured double-stranded RNAs directly dotted on nylon membranes. The p...

Journal: :JAMA 2007
David R Anderson Susan R Kahn Marc A Rodger Michael J Kovacs Tim Morris Andrew Hirsch Eddy Lang Ian Stiell George Kovacs Jon Dreyer Carol Dennie Yannick Cartier David Barnes Erica Burton Susan Pleasance Chris Skedgel Keith O'Rouke Philip S Wells

CONTEXT Ventilation-perfusion (V(dot)Q(dot) lung scanning and computed tomographic pulmonary angiography (CTPA) are widely used imaging procedures for the evaluation of patients with suspected pulmonary embolism. Ventilation-perfusion scanning has been largely replaced by CTPA in many centers despite limited comparative formal evaluations and concerns about CTPA's low sensitivity (ie, chance of...

Journal: :Clinical chemistry 1986
P C Patel L Aubin J Côte

We investigated two techniques of immunoblotting--the Western blot and the dot blot--for use in detecting prostatic acid phosphatase (PAP, EC 3.1.3.2). We used polyclonal antisera to human PAP, produced in rabbits by hyperimmunization with purified PAP, and PAP-specific monoclonal antibodies in the immunoenzymatic protocols. We conclude that PAP can be readily detected by Western blots with use...

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