Preparation of Monoclonal Antibody against Ema-1 and Development of Rapid Serological Detection Method for Theileria equi Infection, Xinjiang, China

10.1645/19-98 ◽  
2020 ◽  
Vol 106 (2) ◽  
pp. 283
Author(s):  
Jingjing Song ◽  
Ruiqi Song ◽  
Panju Wang ◽  
Yang Zhang ◽  
Yan Yan ◽  
...  
2020 ◽  
Vol 19 (5) ◽  
pp. 1283-1291 ◽  
Author(s):  
Yu ZHANG ◽  
Yan-ling GAO ◽  
Wan-qin HE ◽  
Ya-qin WANG ◽  
Ya-juan QIAN ◽  
...  

2018 ◽  
Vol 33 (2) ◽  
pp. 173-180 ◽  
Author(s):  
Minghao Zhang ◽  
Rui Chen ◽  
Xueping Zhou ◽  
Jianxiang Wu

1993 ◽  
Vol 5 (1) ◽  
pp. 33-36 ◽  
Author(s):  
Richard E. Corstvet ◽  
Stephen D. Gaunt ◽  
Phillip A. Karns ◽  
David Burgermeister ◽  
Jere W. McBride ◽  
...  

Four horses were inoculated with Ehrlichia risticii contained in either infected murine P388 D1 cells or heparinized blood from an infected horse. All 4 horses produced serum antibody, plasma antigen, and clinical signs of the disease. An enzyme-linked immunosorbent assay was used to detect antibody in the serum and was also used in conjunction with an anti- E. risticii monoclonal antibody to detect antigenemia. These laboratory and clinical findings were correlated to determine the efficiency of the antigen detection method for discerning E. risticii infection.


1996 ◽  
Vol 22 (6) ◽  
pp. 575-583
Author(s):  
Hiroyuki Yoshizawa ◽  
Susumu Yamauchi ◽  
Takiko Kenjo ◽  
Yoshio Kuroshima ◽  
Tsunehisa Makino

1986 ◽  
Vol 34 (12) ◽  
pp. 1645-1650 ◽  
Author(s):  
M M Leong ◽  
C Milstein ◽  
R Pannell

An anti-peroxidase-anti-biotin hybrid hybridoma rat cell line, capable of producing a bispecific monoclonal antibody, has been derived to explore its use in conjunction with a luminol immunodetection system. Luminescence was detected using x-ray film. The method was sufficiently sensitive and effective, but was less sensitive than autoradiographic methods using high-specific-activity 32P-labeled probes. Exposure times, on the other hand, were of the order of seconds rather than days. The direct binding of both peroxidase and biotin by the bispecific monoclonal antibody is simpler but less sensitive than the more conventional indirect method using a commercial peroxidase coupled with anti-rat antibody as a developing antibody.


Biosensors ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 191
Author(s):  
Weiming Sun ◽  
Lanhua Liu ◽  
Abdul Ghaffar Memon ◽  
Xiaohong Zhou ◽  
Hongwei Zhao

Carbofuran (CBF) is an efficient and broad-spectrum insecticide. As testing indicators for water quality and agricultural products, CBF and its metabolite 3-hydroxy-carbofuran (3-OH-CBF) are regulated by many countries. The detection of CBF and 3-OH-CBF is of great importance for the environment and human health. However, an immunosensor detection method for the simultaneous analysis of CBF and 3-OH-CBF remains unavailable. Herein, we report a waveguide-based fluorescent immunosensor for detecting CBF and 3-OH-CBF, synchronously. The immunosensor is based on a broad-spectrum monoclonal antibody with high binding affinity against CBF and 3-OH-CBF. The linear detection ranges for CBF and 3-OH-CBF are 0.29–2.69 and 0.12–4.59 μg/L, with limits of detection of 0.13 μg/L for CBF and 0.06 μg/L for 3-OH-CBF, respectively. The whole detection process for each cycle is approximately 30 min. The results show a good application prospect for the rapid detection of CBF and 3-OH-CBF in water or agricultural products.


2019 ◽  
Vol 35 (2) ◽  
pp. 227-234 ◽  
Author(s):  
Liqian Guo ◽  
Jiayu Wu ◽  
Rui Chen ◽  
Jian Hong ◽  
Xueping Zhou ◽  
...  

RSC Advances ◽  
2021 ◽  
Vol 11 (36) ◽  
pp. 22005-22013
Author(s):  
Qingbao Yang ◽  
Yanhua Qi ◽  
Jingming Zhou ◽  
Yumei Chen ◽  
Chao Liang ◽  
...  

(1) Water-soluble CdSe/ZnS QDs and an anti-FLE monoclonal antibody were used to prepare a fluorescent probe. (2) Primary rapid detection of FLE residues with visual fluorescent detection method.


2011 ◽  
Vol 18 (12) ◽  
pp. 2181-2182 ◽  
Author(s):  
Brett A. Thibodeaux ◽  
Nathan M. Liss ◽  
Amanda N. Panella ◽  
John T. Roehrig

ABSTRACTDiagnosis of human alphaviral infections relies on serological techniques, such as the immunoglobulin M antibody capture–enzyme-linked immunosorbent assay (MAC-ELISA). We have humanized the alphavirus broadly cross-reactive murine monoclonal antibody 1A4B-6 to create a reagent capable of replacing human positive sera in the MAC-ELISA for diagnosis of human alphaviral infections.


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