Literature DB >> 10803971

Purification of membrane-bound lactoferrin from the human milk fat globule membrane.

J K Cho1, N Azuma, C H Lee, J H Yu, C Kanno.   

Abstract

Although lactoferrin is known as a basic soluble glycoprotein, the presence of the membrane-bound form of this protein has also been demonstrated in human milk. Membrane-bound lactoferrin was extracted from the human milk fat globule membrane with a detergent mixture of 1% Tween-20, 0.5% C12E8, and 0.5 M KCl in 20 mM Tris-HCl (pH 7.4). Lactoferrin in the detergent-soluble fraction was purified by affinity chromatography with Concanavalin A and by hydrophobic chromatography with phenyl-Superose. The purified protein gave a single band of 80 kDa by SDS-PAGE. Its N-terminal amino acid sequence was consistent with that of human lactoferrin.

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Year:  2000        PMID: 10803971     DOI: 10.1271/bbb.64.633

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  3 in total

1.  Evolution of the mammary gland defense system and the ontogeny of the immune system.

Authors:  Armond S Goldman
Journal:  J Mammary Gland Biol Neoplasia       Date:  2002-07       Impact factor: 2.673

Review 2.  Growth hormone and prolactin--molecular and functional evolution.

Authors:  Isabel A Forsyth; Michael Wallis
Journal:  J Mammary Gland Biol Neoplasia       Date:  2002-07       Impact factor: 2.673

3.  The host defense proteome of human and bovine milk.

Authors:  Kasper Hettinga; Hein van Valenberg; Sacco de Vries; Sjef Boeren; Toon van Hooijdonk; Johan van Arendonk; Jacques Vervoort
Journal:  PLoS One       Date:  2011-04-27       Impact factor: 3.240

  3 in total

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