Tumor-derived multiple chaperone enrichment by free-solution isoelectric focusing yields potent antitumor vaccines

Cancer Immunology Immunotherapy

Volumn 49, Issue 9, 2000, Pages 476-484

  Graner, Michael ^a   Raymond, Amy ^a   Akporiaye, Emmanuel ^b   Katsanis, Emmanuel ^a  

^a UNIVERSITY OF ARIZONA COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF ARIZONA   (United States)

Author keywords

Antitumor immunity; Chaperones; Complexes; Isoelectric focusing

Indexed keywords

CANCER VACCINE; CHAPERONE; HEAT SHOCK PROTEIN 70;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANTINEOPLASTIC ACTIVITY; ARTICLE; CELL LYSATE; CONTROLLED STUDY; FEMALE; IMMUNE RESPONSE; ISOELECTRIC FOCUSING; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; TUMOR IMMUNITY; VACCINATION;

ANIMALS; BLOTTING, WESTERN; CANCER VACCINES; CHROMATOGRAPHY; DOSE-RESPONSE RELATIONSHIP, DRUG; ELECTROPHORESIS, POLYACRYLAMIDE GEL; FEMALE; HSP70 HEAT-SHOCK PROTEINS; ISOELECTRIC FOCUSING; LEUKEMIA, B-CELL; MICE; MICE, INBRED BALB C; MOLECULAR CHAPERONES; NEOPLASM TRANSPLANTATION; PROTEIN BINDING; TIME FACTORS; TUMOR CELLS, CULTURED;

EID: 0033762022     PISSN: 03407004     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002620000138     Document Type: Article

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