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Abstract:
To prepare citrinin(CIT)-protein antigen, CIT was conjugated with bovine serum albumin (BSA) by 1, 4-butanediol diglycidyl ether The spleen from the BALB/C mice immunized with CIT-BSA conjugate was used to fuse with the murine SP2/0 By subcloning, a hybridoma cell lines excreting monoclonal antibodies(McAb) against CIT was obtained and named H2-F8 The monoclonal antibodies obtained from hybridoma H2-F8 was of IgM subclass The affinity constant of the McAb to CIT was 4 17x10(8) L/mol and the IC50 value was 0 3 mu g/L Its linear range of the assay was between 0 05 mu g/L and 1 0 mu g/L The cross-reactivity rates were less than 0 1% of other toxins such as ochratoxin A, aflatoxin B1, deoxynivalenol, zearalenone and were less than 0 01% of rubropunctamine and rubropunctamine This work would be helpful for establishing the technology and developing the kit to determine CIT-contaminated samples by ELISA
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PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS
ISSN: 1000-3282
CN: 11-2161/Q
Year: 2010
Issue: 11
Volume: 37
Page: 1248-1253
0 . 2 3 6
JCR@2010
0 . 2 0 0
JCR@2023
JCR Journal Grade:4
CAS Journal Grade:4
Cited Count:
WoS CC Cited Count: 5
SCOPUS Cited Count: 8
ESI Highly Cited Papers on the List: 0 Unfold All
WanFang Cited Count:
Chinese Cited Count:
30 Days PV: 0
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