نتایج جستجو برای: sandwich elisa

تعداد نتایج: 54982  

Journal: :Nepal Medical College journal : NMCJ 2009
S Ishiyamna K Ono S K Rai S Uga

Diagnosis of larval migrans (LM) is usually done by immunodiagnostic methods. These methods, however, simply show the presence or absence of antibody but not the active infection of the patients. Therefore, we aimed to establish a diagnostic method for detecting circulating Toxocara canis antigen using a sandwich, ELISA. Monoclonal antibodies (MAb) were produced against the excretory-secretory ...

Journal: :Journal of Immunological Methods 2010

Journal: :Journal of clinical microbiology 1988
N T Foged J P Nielsen K B Pedersen

An enzyme-linked immunosorbent assay (ELISA) was developed for the rapid and simple differentiation of toxigenic from nontoxigenic strains of Pasteurella multocida. The sandwich ELISA is based on two different murine monoclonal antibodies with specificity for the P. multocida toxin. The ELISA, which is now used as a routine test in Denmark, has several advantages compared with previously descri...

Journal: :Analytical biochemistry 2010
Ming Kei Chung Jacques Riby He Li Anthony T Iavarone Evan R Williams Yuxin Zheng Stephen M Rappaport

Adducts of benzo[a]pyrene-diolepoxide (BPDE) with blood nucleophiles have been used as biomarkers of exposure to polycyclic aromatic hydrocarbons (PAHs). The most popular such assay is a competitive enzyme-linked immunosorbent assay (ELISA) that employs monoclonal antibody 8E11 to detect benzo[a]pyrene tetrols following hydrolysis of BPDE adducts from lymphocyte DNA or human serum albumin (HSA)...

Journal: :archives of razi institute 2016
m. torabi a. haadi e. asli m. aminian f. esmaily

in the present study, seven isolates of haemophilus influenzae type b were cultured in four different media to compare growth rate and capsule production. four liquid media namely brain heart infusion broth (bhi), trypticase soy broth (tsb), mueller hinton broth (mhb) and gonococci broth (gc) with added supplements (1% hemoglobin, 1% isovitalex) were used. the growth was measured by colony coun...

Journal: :Analytical biochemistry 2011
Cheryl L Baird Ruimin Tan Christopher J Fischer Kristin D Victry Richard C Zangar Karin D Rodland

Sandwich enzyme-linked immunosorbent assay (ELISA) microarrays can simultaneously quantify the levels of multiple diagnostic targets in a biological sample. However, as with traditional ELISA diagnostics, endogenous antibodies in patient sera can cause interference. We demonstrate here that reducing the diagnostic capture antibody to its minimal functional unit (i.e., a single-chain antibody fr...

Journal: :Clinical chemistry 2015
Kazuya Omi Tsuyoshi Ando Takuya Sakyu Takashi Shirakawa Yoshiaki Uchida Asako Oka Nobuyuki Ise Katsumi Aoyagi Katsutoshi Goishi

BACKGROUND Small molecules classified as haptens are generally measured by competitive immunoassay, which is theoretically inferior to noncompetitive sandwich immunoassay in terms of sensitivity and specificity. We created a method for developing sandwich immunoassays to measure haptens on the basis of antimetatype antibodies. METHODS We generated antimetatype monoclonal antibodies against a ...

Journal: :Journal of clinical microbiology 2012
Yongjun Jiao Xiaoyan Zeng Xiling Guo Xian Qi Xiao Zhang Zhiyang Shi Minghao Zhou Changjun Bao Wenshuai Zhang Yan Xu Hua Wang

The recent emergence of the human infection confirmed to be caused by severe fever with thrombocytopenia syndrome virus (SFTSV) in China is of global concern. Safe diagnostic immunoreagents for determination of human and animal seroprevalence in epidemiological investigations are urgently needed. This paper describes the cloning and expression of the nucleocapsid (N) protein of SFTSV. An N-prot...

Journal: :Journal of clinical pathology 1997
M D Thomas G G McIntosh J J Anderson D M McKenna A H Parr R Johnstone T W Lennard C H Horne B Angus

AIM To develop a highly sensitive and specific enzyme linked immunosorbent assay (ELISA) system for analysis of p53 protein in cancer lysates. METHODS The anti-p53 monoclonal antibodies DO7, 1801, BP53.12, and 421, and anti-p53 polyclonal antiserum CM1 were assessed by immunohistochemistry and western blot analysis to identify those most suitable for determining p53 status of cancer cells. An...

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