Monitoring the localization of MAP1LC3B by indirect immunofluorescence

Cold Spring Harbor Protocols

Volumn 2015, Issue 8, 2015, Pages 751-755

  Ktistakis, Nicholas T ^a  

^a BABRAHAM INSTITUTE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

FLUORESCENT DYE; MAMMALIAN TARGET OF RAPAMYCIN; MICROTUBULE ASSOCIATED PROTEIN; HYBRID PROTEIN; MAP1LC3B PROTEIN, HUMAN; PHOTOPROTEIN;

ARTICLE; AUTOPHAGOSOME; AUTOPHAGY; CONTROLLED STUDY; EMBRYO; FLUORESCENCE MICROSCOPY; GENE; GENE LOCATION; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOFLUORESCENCE; LC3B GENE; PLASMID; CELL LINE; CHEMISTRY; CYTOSOL; GENE FUSION; GENETICS; INDIRECT FLUORESCENT ANTIBODY TECHNIQUE; PHAGOSOME; PROCEDURES; STAINING;

MAMMALIA;

ARTIFICIAL GENE FUSION; AUTOPHAGY; CELL LINE; CYTOSOL; FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT; HUMANS; LUMINESCENT PROTEINS; MICROTUBULE-ASSOCIATED PROTEINS; PHAGOSOMES; RECOMBINANT FUSION PROTEINS; STAINING AND LABELING;

EID: 84938696943     PISSN: 19403402     EISSN: 15596095     Source Type: Journal    
DOI: 10.1101/pdb.prot086264     Document Type: Article

References (1)

1. Chittaranjan S, Bortnik S, Gorski SM. 2015. Monitoring autophagic flux by using lysosomal inhibitors and western blotting of endogenous LC3B. Cold Spring Harb Protoc doi: 10.1101/pdb.prot086256.