Electrophoretic mobility-shift and super-shift assays for studies and characterization of protein-DNA complexes

Methods in Molecular Biology

Volumn 977, Issue , 2013, Pages 159-167

  Parés Matos, Elsie I ^a  

^a NONE

Author keywords

DNA protein interaction; Electrophoretic mobility shift assay; Nuclear extract; Promoter of NF IL6 gene; Super shift assay

Indexed keywords

GENOMIC DNA; TRANSCRIPTION FACTOR; CCAAT ENHANCER BINDING PROTEIN BETA; CEBPB PROTEIN, HUMAN; CELL EXTRACT; DNA; DNA BINDING PROTEIN;

ARTICLE; DNA DETERMINATION; DNA PROTEIN COMPLEX; GEL MOBILITY SHIFT ASSAY; GENE CONTROL; GENE EXPRESSION; GENE EXPRESSION REGULATION; HUMAN; NONHUMAN; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN ANALYSIS; REGULATORY DNA SEQUENCE; BINDING SITE; CELL FRACTIONATION; CELL LINE; CELL NUCLEUS; CHEMISTRY; GENETICS; ISOLATION AND PURIFICATION; METHODOLOGY; POLYACRYLAMIDE GEL ELECTROPHORESIS; PROTEIN BINDING; STAINING;

BINDING SITES; CCAAT-ENHANCER-BINDING PROTEIN-BETA; CELL EXTRACTS; CELL FRACTIONATION; CELL LINE; CELL NUCLEUS; DNA; DNA-BINDING PROTEINS; ELECTROPHORESIS, POLYACRYLAMIDE GEL; ELECTROPHORETIC MOBILITY SHIFT ASSAY; HUMANS; PROMOTER REGIONS, GENETIC; PROTEIN BINDING; STAINING AND LABELING;

MLCS; MLOWN;

EID: 84880990432     PISSN: 10643745     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-62703-284-1_12     Document Type: Article

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