Each GPI-anchored protein species forms a specific lipid raft depending on its GPI attachment signal

Glycoconjugate Journal

Volumn 32, Issue 7, 2015, Pages 531-540

  Miyagawa Yamaguchi, Arisa ^a   Kotani, Norihiro ^b   Honke, Koichi ^a  

^a KOCHI MEDICAL SCHOOL   (Japan)

^b SAITAMA MEDICAL UNIVERSITY   (Japan)

Author keywords

EMARS; Fluorescein tyramide; HRP; N glycosylation; Visualization of co clustering molecules

Indexed keywords

AZIDE; DECAY ACCELERATING FACTOR; FLUORESCEIN ARYLAZIDE; FLUORESCEIN CONJUGATED TYRAMIDE; GLYCOSYLPHOSPHATIDYLINOSITOL ANCHORED PROTEIN; HORSERADISH PEROXIDASE; HYDROGEN PEROXIDE; REAGENT; THY 1 ANTIGEN; UNCLASSIFIED DRUG; FLUORESCEIN; MEMBRANE PROTEIN;

ANALYTIC METHOD; ARTICLE; CHEMICAL LABELING; CONFOCAL MICROSCOPY; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; ENZYME MECHANISM; ENZYME MEDIATED ACTIVATION OF RADICAL SOURCE METHOD; GOLGI MEMBRANE; LIPID RAFT; PRIORITY JOURNAL; PROTEIN GLYCOSYLATION; SIGNAL TRANSDUCTION; ANIMAL; CELL LINE; CELL MEMBRANE; CHEMISTRY; GENETICS; GLYCOSYLATION; GOLGI COMPLEX; METABOLISM;

ANIMALS; ANTIGENS, CD55; CELL LINE; CELL MEMBRANE; ENDOPLASMIC RETICULUM; FLUORESCEIN; GLYCOSYLATION; GOLGI APPARATUS; HORSERADISH PEROXIDASE; MEMBRANE MICRODOMAINS; MEMBRANE PROTEINS;

EID: 84944277806     PISSN: 02820080     EISSN: 15734986     Source Type: Journal    
DOI: 10.1007/s10719-015-9595-5     Document Type: Article

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