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Technical Briefs |
1 Lipoprotein and Atherosclerosis Group, University of Ottawa Heart Institute, Ottawa Civic Hospital, Ottawa, Ontario, K1Y 4E9 Canada
2 The Gladstone Institute of Cardiovascular Disease, Cardiovascular Research Institute, University of California, San Francisco, CA 94141-9100
3 Département des Sciences Biologiques, Université du Québec, Montréal, CP 8888, Québec, H3C 3P8 Canada
aauthor for correspondence: fax 415-285-5632, e-mail rraffai@gladstone.ucsf.edu
| The first 20% of the full text of this article appears below. |
Numerous methods have been described to determine the apolipoprotein E (apoE) phenotype or genotype of individuals (1)(2). These techniques are relatively time-consuming, and interpretation of the results can be difficult. Here, we report the development of a rapid and specific antibody-based test for the identification of the apoE2 isoform. Previously, we characterized the binding properties of a panel of anti-human apoE monoclonal antibodies (mAbs) (3)(4)(5). The locations of epitopes of selected mAbs from the panel are presented in Fig. 1A
. Although neither mAb 6C5 nor 3H1 showed apoE isoform specificity, mAb 2E8 recognized an epitope that includes the apoE LDL receptor-binding site and resembles the LDL receptor in terms of its fine specificity.
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