Improvement of the chromatin immunoprecipitation (ChIP) assay by DNA fragment size fractionation

BioTechniques

Volumn 31, Issue 4, 2001, Pages 740-742

  Johnson, T A ^a   Wilson, H L ^a   Roesler, W J ^a  

^a UNIVERSITY OF SASKATCHEWAN   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CCAAT ENHANCER BINDING PROTEIN; DNA FRAGMENT; PHOSPHOENOLPYRUVATE CARBOXYKINASE (GTP); TRANSCRIPTION FACTOR;

ANIMAL CELL; ARTICLE; BINDING SITE; CHROMATIN; CONTROLLED STUDY; FRACTIONATION; IMMUNOPRECIPITATION; NONHUMAN; POLYMERASE CHAIN REACTION; PROMOTER REGION; PROTEIN DNA BINDING; ULTRASOUND;

EID: 0034788297     PISSN: 07366205     EISSN: None     Source Type: Journal    
DOI: 10.2144/01314bm05     Document Type: Article

References (6)

1. A simplified formaldehyde fixation and immunoprecipitation technique for studying protein-DNA interactions
2. DNA fragment purification: Removal of agarose 10 minutes after electrophoresis
3. Mapping chromosomal proteins in vivo by formaldehyde-crosslinkedchromatin immunoprecipitation
4. Analysis of chromatin structure by in vivo formaldehyde cross-linking
5. The role of the CCAAT/enhancer binding protein in the transcriptional regulation of the gene for phosphoenolpyruvate carboxykinase (GTP)
6. Characterization of the liver-specific component of the cAMP response unit of the phosphoenolpyruvate carboxykinase (GTP) gene promoter