Isolating recombinant antibodies against specific protein morphologies using atomic force microscopy and phage display technologies

Protein Engineering, Design and Selection

Volumn 19, Issue 11, 2006, Pages 497-502

  Barkhordarian, Hedieh ^a   Emadi, Sharareh ^a   Schulz, Philip ^a   Sierks, Michael R ^a,b  

^a Arizona State University   (United States)

^b Box 876006 ^*  (United States)

Author keywords

Antibodies; Atomic force microscopy; Bio panning; phage display; Protein morphology

Indexed keywords

ANTIGENS; ATOMIC FORCE MICROSCOPY; DISEASES; OLIGOMERS; TOXICITY;

BIO-PANNING; PHAGE DISPLAY; PROTEIN MORPHOLOGY; RECOMBINANT ANTIBODY;

ANTIBODIES;

ALPHA SYNUCLEIN; OLIGOMER; RECOMBINANT ANTIBODY; SINGLE CHAIN FRAGMENT VARIABLE ANTIBODY;

ANTIBODY ISOLATION; ANTIBODY SPECIFICITY; ANTIGEN BINDING; ARTICLE; ATOMIC FORCE MICROSCOPY; CONTROLLED STUDY; DISEASE COURSE; DNA SEQUENCE; ELUTION; ENZYME LINKED IMMUNOSORBENT ASSAY; FIBER; LEWY BODY; MORPHOLOGY; NONHUMAN; PARKINSON DISEASE; PHAGE DISPLAY; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN EXPRESSION; PROTEIN FOLDING; PROTEIN PURIFICATION;

ALPHA-SYNUCLEIN; ANTIBODIES; ANTIGENS; BASE SEQUENCE; HUMANS; IMMUNOGLOBULIN FC FRAGMENTS; MICROSCOPY, ATOMIC FORCE; PARKINSON DISEASE; PEPTIDE LIBRARY; PLASMIDS; PROTEIN ENGINEERING; PROTEINS; RECOMBINANT PROTEINS;

EID: 33750291199     PISSN: 17410126     EISSN: 17410134     Source Type: Journal    
DOI: 10.1093/protein/gzl036     Document Type: Article

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