Studies of the pattern recognition molecule H-ficolin: Specificity and purification

Journal of Biological Chemistry

Volumn 287, Issue 11, 2012, Pages 8071-8081

  Zacho, Rikke M ^a   Jensen, Lisbeth ^a   Terp, Randi ^a   Jensenius, Jens C ^a   Thiel, Steffen ^a  

^a AARHUS UNIVERSITY   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYL SALICYLIC ACID; ARTIFICIAL TARGETS; BOVINE SERUM ALBUMINS; CALCIUM IONS; COMPLEMENT SYSTEMS; INNATE IMMUNE SYSTEMS; ION EXCHANGE CHROMATOGRAPHY; LIGAND BINDING; NACL CONCENTRATION; SERINE PROTEASE; SERUM ALBUMIN; SODIUM ACETATE; STRUCTURAL CHANGE;

AFFINITY CHROMATOGRAPHY; AMINO ACIDS; BACILLI; BODY FLUIDS; CHROMATOGRAPHIC ANALYSIS; GEL PERMEATION CHROMATOGRAPHY; MAMMALS; MOLECULES; OLIGOMERIZATION; OLIGOMERS; PATTERN RECOGNITION; SODIUM CHLORIDE;

PURIFICATION;

ACETIC ACID; ACETURIC ACID; ACETYL GROUP; ACETYLCYSTEINE; ACETYLSALICYLIC ACID; BOVINE SERUM ALBUMIN; CALCIUM ION; COMPLEMENT COMPONENT C4; FICOLIN; FUNCTIONAL GROUP; GLYCINE DERIVATIVE; H FICOLIN; H FICOLIN MASP 2 PROTEIN; HYBRID PROTEIN; MASP 2 PROTEIN; N ACETYLGALACTOSAMINE; N ACETYLGLUCOSAMINE; SODIUM CHLORIDE; UNCLASSIFIED DRUG;

AEROCOCCUS VIRIDANS; AFFINITY CHROMATOGRAPHY; ANTIGEN SPECIFICITY; ARTICLE; COMPLEMENT ACTIVATION; CONCENTRATION RESPONSE; CONTROLLED STUDY; GEL PERMEATION CHROMATOGRAPHY; HUMAN; ION EXCHANGE CHROMATOGRAPHY; LIGAND BINDING; MOLECULAR WEIGHT; MOUSE; NONHUMAN; OLIGOMERIZATION; PATTERN RECOGNITION; PRECIPITATION; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN PURIFICATION; SERUM;

ACETYLCYSTEINE; ACETYLGALACTOSAMINE; ACETYLGLUCOSAMINE; AEROCOCCUS; ANIMALS; ASPIRIN; CATTLE; COMPLEMENT C4; COMPLEMENT PATHWAY, MANNOSE-BINDING LECTIN; GLYCOPROTEINS; HUMANS; IMMUNITY, INNATE; LECTINS; MANNOSE-BINDING PROTEIN-ASSOCIATED SERINE PROTEASES; MICE; MULTIPROTEIN COMPLEXES; PROTEIN BINDING; SERUM ALBUMIN, BOVINE; SODIUM ACETATE;

AEROCOCCUS VIRIDANS; BOVINAE;

EID: 84858065747     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M111.301044     Document Type: Article

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