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. 2009 Jan 12;184(1):173–183. doi: 10.1083/jcb.200801071

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© 2009 Johswich et al.

This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).

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Figure 7. — Protein domains of β4GalNAcTB involved in the interaction with GABPI. Hybrids of Flag-β4GalNAcTA (red) and -B (blue) were cloned by domain swapping of the cytoplasmic (Cyt) and transmembrane domain (TMD), stem region, and catalytic domain (Cat) as illustrated and expressed in HEK293 with and without GABPI. The intracellular localization was analyzed by indirect immunofluorescence using α-mannosidase II and calnexin as markers for Golgi and ER, respectively.