Author/Authors :
Zhou، نويسنده , , Yu and Li، نويسنده , , Yan-Song and Pan، نويسنده , , Feng-Guang and Zhang، نويسنده , , Yuan-Yuan and Lu، نويسنده , , Shiying and Ren، نويسنده , , Honglin and Li، نويسنده , , Zhao-Hui and Liu، نويسنده , , Zeng-Shan and Zhang، نويسنده , , Jun-Hui، نويسنده ,
Abstract :
Brevetoxin B (PbTx-2) was covalently linked to carrier protein bovine serum albumin and human gamma globulin. A monoclonal antibody against PbTx-2, which showed high cross-reactivity values with PbTx-1, PbTx-3 and PbTx-9 (more than 89%) was obtained from ascites and some characteristics of monoclonal antibody were studied. An direct competitive enzyme-linked immunosorbent assay (ELISA) for detection of PbTxs was developed, which showed an IC50 value of 5.3 ng mL−1 with a detection limit of 0.6 ng well−1. The recoveries of PbTxs from cockle (88.4%–102.3%) and oyster (89.4%–104.3%) demonstrated that the matrices of cockle and oyster where PbTxs are found do not interfere with the assay. The newly developed competitive ELISA appears to be a reliable and useful method for mass monitoring of PbTxs in mollusk.
Keywords :
Recovery , Hybridoma cell line , monoclonal antibody , Enzyme-linked immunosorbent assay , Brevetoxin , cross-reactivity