A sensitivity-enhanced heterologous immunochromatographic assay based on a monoclonal antibody for the rapid detection of histamine in saury samples

RSC Advances ◽  
2015 ◽  
Vol 5 (96) ◽  
pp. 78833-78840 ◽  
Author(s):  
Lin Luo ◽  
Jin-Yi Yang ◽  
Zhi-Li Xiao ◽  
Dao-Ping Zeng ◽  
Yong-Jun Li ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
Rapid Detection ◽  
Immunochromatographic Assay

An immunochromatograhic strip for rapid detection of histamine based on a sensitive monoclonal antibody against p-nitrobenzoylated histamine was firstly reported.

Development of a monoclonal antibody-based immunochromatographic strip for the rapid detection of tigecycline in human serum

2021 ◽  
Author(s):  
Chuanlai Xu ◽  
qianqian lu ◽  
Xin-Xin Xu ◽  
Shanshan Song ◽  
aihong wu ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
Human Serum ◽  
Rapid Detection ◽  
Immunochromatographic Assay ◽  
Immunochromatographic Strip

In this study, a gold labelled immunochromatographic assay was developed to detect tigecycline (TGC) in human serum. For this purpose, an anti-TGC monoclonal antibody, 2G7, was produced and characterized, and...

scholarly journals Development of a fluorescent immunochromatographic assay based on quantum dots for the detection of fleroxacin

RSC Advances ◽  
2021 ◽  
Vol 11 (36) ◽  
pp. 22005-22013
Author(s):  
Qingbao Yang ◽  
Yanhua Qi ◽  
Jingming Zhou ◽  
Yumei Chen ◽  
Chao Liang ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
Quantum Dots ◽  
Fluorescent Probe ◽  
Rapid Detection ◽  
Detection Method ◽  
Water Soluble ◽  
Fluorescent Detection ◽  
Immunochromatographic Assay

(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.

A novel chemiluminescent immunochromatographic assay strip for rapid detection of mercury ions

2017 ◽  
Vol 9 (16) ◽  
pp. 2401-2406 ◽  
Author(s):  
Xiaomei Wang ◽  
Fengquan Liu ◽  
Qian Shao ◽  
Zhengrong Yin ◽  
Limin Wang ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
Rapid Detection ◽  
Immunochromatographic Assay ◽  
Mercury Ions

A chemiluminescent immunochromatographic assay strip for rapid detection of Hg2+ was developed by using an anti-Hg2+ monoclonal antibody that could directly recognize Hg2+.

scholarly journals Preparation of a monoclonal antibody against testosterone and its use in development of an immunochromatographic assay

2016 ◽  
Vol 27 (4) ◽  
pp. 547-558 ◽  
Author(s):  
Zhongxing Wang ◽  
Shuzhen Zou ◽  
Changrui Xing ◽  
Shanshan Song ◽  
Liqiang Liu ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
Immunochromatographic Assay

scholarly journals Rapid Detection of PBP2a in Staphylococci from Shortly Incubated Subcultures of Positive Blood Cultures by an Immunochromatographic Assay

2021 ◽  
Author(s):  
Natalia Kolesnik-Goldmann ◽  
Elias Bodendoerfer ◽  
Kim Röthlin ◽  
Sebastian Herren ◽  
Frank Imkamp ◽  
...  
Keyword(s):  
Antibiotic Resistance ◽  
Antimicrobial Resistance ◽  
Patient Care ◽  
Rapid Detection ◽  
Resistance Mechanisms ◽  
Blood Cultures ◽  
Immunochromatographic Assay ◽  
Economic Costs ◽  
Major Threat ◽  
Improving Patient Care

Antibiotic resistance poses a major threat to health and incurs high economic costs worldwide. Rapid detection of resistance mechanisms can contribute to improving patient care and preventing the dissemination of antimicrobial resistance.

Listeriolysin O-Based Latex Agglutination Test for the Rapid Detection of Listeria monocytogenes in Foods

1997 ◽  
Vol 60 (9) ◽  
pp. 1038-1040 ◽  
Author(s):  
GHASSAN M. MATAR ◽  
PEGGY S. HAYES ◽  
WILLIAM F. BIBB ◽  
BALA SWAMINATHAN
Keyword(s):  
Monoclonal Antibody ◽  
Listeria Monocytogenes ◽  
Rapid Detection ◽  
Rapid Test ◽  
Food Samples ◽  
Cross Reactivity ◽  
Latex Agglutination ◽  
Listeriolysin O ◽  
Agglutination Assay ◽  
Latex Beads

A latex agglutination-based test for the rapid detection of Listeria monocytogenes in foods was developed. An antilisteriolysin O (LLO) monoclonal antibody (HID5E12D7; IgG2b) covalently bound to polystyrene amidine-modified latex beads was used in a slide agglutination assay. The latex reagent detected 0.1 ng/ml of LLO in phosphate-buffered saline plus bovine serum albumin. It reacted with culture supernatants of L. monocytogenes but not with other Listeria species or Streptococcus groups A through G. The listeriolysin O latex agglutination assay (LLOLAT) was applied to 24-h and 48-h USDA primary enrichment cultures of 208 food samples obtained from refrigerators of listeriosis patients enrolled in a study to determine the role of foods in sporadic listeriosis. Of 19 samples positive by cultural techniques, 17 were positive by the LLOLAT. Cultures with low (<0.3 CFU/g) levels of L. monocytogenes were positive in the LLOLAT. No cross-reactivity occurred when using a heterogeneous monoclonal antibody. The LLOLAT is a sensitive, specific and rapid test and may be useful for screening foods for L. monocytogenes.

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