Sensitive enzyme-linked immunosorbent assay and rapid one-step immunochromatographic strip for fumonisin B1 in grain-based food and feed samples

2010 ◽  
Vol 90 (6) ◽  
pp. 1020-1026 ◽  
Author(s):  
Chang-Min Shiu ◽  
Jing-Jhih Wang ◽  
Feng-Yih Yu

1999 ◽  
Vol 22 (12) ◽  
pp. 1266-1270 ◽  
Author(s):  
Tomofumi KUROKAWA ◽  
Tetsuo HOSHINO ◽  
Tsuneo ODA ◽  
Kazuhiro SAITO ◽  
Yasuaki OGAWA




2003 ◽  
Vol 24 (2) ◽  
pp. 205-217 ◽  
Author(s):  
Tulsidas G. Shrivastav ◽  
Anupam Basu ◽  
Kiran P. Kariya


2009 ◽  
Vol 637 (1-2) ◽  
pp. 273-278 ◽  
Author(s):  
Giampiero Scortichini ◽  
Loredana Annunziata ◽  
Valeria Di Girolamo ◽  
Roberta Buratti ◽  
Roberta Galarini


2018 ◽  
Vol 34 (1) ◽  
pp. 51-56 ◽  
Author(s):  
Masanori ISHII ◽  
Pattarachaya PREECHAKASEDKIT ◽  
Kentaro YAMADA ◽  
Orawon CHAILAPAKUL ◽  
Koji SUZUKI ◽  
...  


Toxins ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 551 ◽  
Author(s):  
Sato ◽  
Takaishi ◽  
Yasumoto ◽  
Watabe

A novel polyclonal antibody against tetrodotoxin (TTX) was raised using its haptenic antigen, where 4,9-anhydroTTX was reacted with 1,2-ethanedithiol and this derivative was further reacted with keyhole limpet hemocyanin (KLH). This newly designed antigen (KLH-TTX) was inoculated into rabbits, resulting in the production of the specific polyclonal antibody, which reacted well with TTX and its analogs, 4-epiTTX, 11-oxoTTX and 5,6,11-trideoxyTTX, except for 4,9-anhydroTTX. The enzyme-linked immunosorbent assay (ELISA) system using this specific antibody was also developed in the present study. This newly developed polyclonal antibody with analytical procedures using direct one-step ELISA is useful to detect TTX and its analogs in toxic organisms and also disclose the mechanisms involved in their metabolic pathways and accumulation of TTX.



1987 ◽  
Vol 17 (1-2) ◽  
pp. 141-148 ◽  
Author(s):  
F. Wielaard ◽  
J. Scherders ◽  
C. Dagelinckx ◽  
P. Gausset




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