Capillary electrophoretic mobility shift assay for binding of DNA with NFAT3, a transcription factor from H9c2 cardiac myoblast cells

Electrophoresis

Volumn 32, Issue 16, 2011, Pages 2174-2180

  Park, Soo Hyun ^a,b   Ban, Eunmi ^a   Song, Eun Joo ^a   Lee, Hyunjung ^a   Chung, Doo Soo ^b   Yoo, Young Sook ^a  

^a Korea Institute of Science and Technology   (South Korea)

^b Seoul National University   (South Korea)

Author keywords

Binding interaction; Cardiac hypertrophy; CEMSA; H9c2; NFAT

Indexed keywords

BINDING ENERGY; CYTOLOGY; ELECTROPHORETIC MOBILITY; HEART; PATHOLOGY; TRANSCRIPTION; TRANSCRIPTION FACTORS;

BINDING INTERACTION; CARDIAC HYPERTROPHY; CELL-BE; CELL/B.E; CELL/BE; CEMSA; ELECTROPHORETIC MOBILITY-SHIFT ASSAYS; ENDOTHELIN-1; H9C2; NUCLEAR FACTOR OF ACTIVATED T CELLS;

DNA;

DNA; ENDOTHELIN 1; TRANSCRIPTION FACTOR NFAT3;

ANIMAL CELL; ARTICLE; BINDING AFFINITY; CALCIUM SIGNALING; CAPILLARY ELECTROPHORESIS; CELL LINE; COMPETITIVE ABILITY; CONTROLLED STUDY; DNA BINDING; GEL MOBILITY SHIFT ASSAY; HEART MUSCLE; HEART VENTRICLE HYPERTROPHY; MIGRATION; MYOBLAST; NERVOUS SYSTEM; NONHUMAN; RAT; REACTION TIME; SEPARATION TECHNIQUE; SKELETAL MUSCLE; WESTERN BLOTTING;

EID: 80051737538     PISSN: 01730835     EISSN: 15222683     Source Type: Journal    
DOI: 10.1002/elps.201100091     Document Type: Article

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