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. 2016 Dec 5;26(12):1284–1296. doi: 10.1093/glycob/cww075

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© The Author 2016. Published by Oxford University Press.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Fig. 4. — Purification of IIH6+ proteins from rabbit kidney. IIH6 immunoreactivity of rabbit kidney extracts (A and B, Triton extract; C and D, urea extract) applied to columns (A and C, DEAE-cellulose; B and D, IIH6-Sepharose), and samples separated by the columns (the void and eluted fractions). The fractions TEA1-3 and NaCl-TEA1-3 derived from the Triton extract were subjected to trypsin digestion and analyzed by MS (Table II). In the cases of the TEA-2 and NaCl-TEA1-3 fractions derived from urea extract, the areas in the SDS-PAGE gels indicated by squared brackets were excised and analyzed by in-gel trypsin digestion and subsequent MS (Table III).