LC3- and p62-based biochemical methods for the analysis of autophagy progression in mammalian cells

Methods

Volumn 75, Issue , 2015, Pages 13-18

  Jiang, Peidu ^a,b   Mizushima, Noboru ^a  

^a UNIVERSITY OF TOKYO   (Japan)

^b TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

Author keywords

Autophagic flux; Autophagy; Immunoblotting; LC3; P62; SQSTM1

Indexed keywords

PROTEIN; PROTEIN P62; SEQUESTOSOME 1; UNCLASSIFIED DRUG; HEAT SHOCK PROTEIN; MAP1LC3 PROTEIN, MOUSE; MICROTUBULE ASSOCIATED PROTEIN; SIGNAL TRANSDUCING ADAPTOR PROTEIN; SQSTM1 PROTEIN, MOUSE;

ANIMAL CELL; ARTICLE; AUTOPHAGY; CHEMICAL ANALYSIS; CLINICAL PROTOCOL; CONCENTRATION (PARAMETERS); EMBRYO; HUMAN; HUMAN CELL; IMMUNOBLOTTING; MAMMAL CELL; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; ANIMAL; CELL LINE; GENETICS; LYSOSOME; MAMMAL; METABOLISM; MOLECULAR BIOLOGY; PROCEDURES;

MAMMALIA;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ANIMALS; AUTOPHAGY; CELL LINE; HEAT-SHOCK PROTEINS; LYSOSOMES; MAMMALS; MICE; MICROTUBULE-ASSOCIATED PROTEINS; MOLECULAR BIOLOGY;

EID: 84924367293     PISSN: 10462023     EISSN: 10959130     Source Type: Journal    
DOI: 10.1016/j.ymeth.2014.11.021     Document Type: Article

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