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Purification of E. coli-synthesized Pan proteins and development of a Pan-specific monoclonal antibody.

作者信息

Vierra C A, Xin X Q, Jacobs Y T, Campbell J M, Shen L P, Rutter W J, Nelson C

机构信息

Department of Biochemistry, University of California, Riverside 92521.

出版信息

Hybridoma. 1994 Jun;13(3):191-7. doi: 10.1089/hyb.1994.13.191.

DOI:10.1089/hyb.1994.13.191
PMID:7523277
Abstract

The helix-loop-helix (HLH) transcription factors, Pan-1 (E47) and Pan-2 (E12), are produced by the mechanism of alternative transcript splicing. Pan-1 and Pan-2 were expressed in Escherichia coli, and a purification scheme was developed. Purified Pan-2 was used to immunize Smith-Webster mice and a hybridoma was generated that produced a monoclonal antibody (Yae) that specifically recognized both native and denatured Pan-1 and Pan-2. Deletion mapping and sequence transfer studies have localized the determinant recognized by the Yae antibody to the region 195-208 of Pan-2. This region is conserved in Pan-1 and Pan-2. The Yae antibody recognized in vitro-synthesized ITF-1, a third E2A (Pan) gene product also produced by the mechanism of alternative RNA splicing, but did not recognize the related HLH proteins, ITF-2, REB alpha, or REB beta. By Western blot assay of pancreatic acinar cells, the Yae antibody detected a single protein species of 72 kD that comigrated with in vitro-synthesized Pan-1 and Pan-2.

摘要

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