Development of a Monoclonal Antibody-based Immunohistochemistry Method for Bse Surveillance in China.
From: National BSE Reference Laboratory, National Diagnostic Center for Exotic Animal Diseases, National Animal Quarantine Institute MOA, 266032, Qingdao, China.
Annals of the New York Academy of Sciences
- Publish Date: Oct 2006
- ISSN: 0077-8923
- Volume: 1081
- Issue:
- Pages: 112-23
- Medium: Print
- Language: English
- Citation (JAMA): Wu Xiaodong, Wang Zhiliang, Liu Yutian, et al. Development of a Monoclonal Antibody-based Immunohistochemistry Method for Bse Surveillance in China.. Ann. N. Y. Acad. Sci. Oct 2006;1081:112-23
Abstract
Five hybridoma cell lines secreting anti-PrP antibodies were established from the fusion between mouse myeloma Sp2/0 and spleen cells from mice immunized with recombinant Chinese Luxi yellow cattle (Bos taurus, Luxi) PrP (24-234) or recombinant Chinese small-tailed Han sheep PrP (94-227). According to their Western blot reactivity, five monoclonal antibodies (mAbs) could be divided into two groups. Group A, mAbs 1H2, 4C6, and 4C11 recognized re-PrP, PrP(C), and PrP(Sc) from both bovine and sheep. Group B, mAbs 2H3 and 4H10 only recognized re-PrP and PrP(Sc) of sheep, and especially, these two mAbs could not recognize PrP(C) from both bovine and sheep. In immunohistochemistry (IHC) test, mAb 4C11 immunostained the PrP(Sc) accumulation in tissue sections from BSE cattle and Scrapie sheep, and compared with mAb 6H4, it had the same immunohistochemical pattern. An IHC method based on mAb 4C11 for the detection of BSE was established and had been applied for the long-term surveillance of BSE in China. From 2001 to 2004, 12,692 samples from the whole country had been tested and all had negative results.
Mesh Headings (Keywords): Animals, Antibodies, Monoclonal, Blotting, Western, Brain, Cattle, China, Encephalopathy, Bovine Spongiform, Immunohistochemistry, PrPSc Proteins, Scrapie, Sensitivity and Specificity, Sentinel Surveillance, Sheep
Check for Full Text / PubMed Unique Identifier (PMID): 17135500
This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.
Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.
The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.
