Electrophoretic mobility shift scanning using an automated infrared DNA sequencer

BioTechniques

Volumn 31, Issue 5, 2001, Pages 1056-1062

  Sano, M ^a   Ohyama, A ^a   Takase, K ^a   Yamamoto, M ^a   Machida, M ^a  

^a NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

COOLING; DNA; GELS; PROTEINS; RADIOISOTOPES;

GEL PLATES;

ELECTROPHORESIS;

DNA BINDING PROTEIN; FLUORESCENT DYE; TRANSCRIPTION FACTOR;

ARTICLE; ASPERGILLUS ORYZAE; AUTOMATION; DNA PROTEIN COMPLEX; DNA SEQUENCE; ELECTROPHORETIC MOBILITY; FUNGUS; INFRARED RADIATION; NONHUMAN; NUCLEOTIDE SEQUENCE; PROMOTER REGION; PROTEIN BINDING; SAFETY; SEQUENCE ANALYSIS;

EID: 0035173032     PISSN: 07366205     EISSN: None     Source Type: Journal    
DOI: 10.2144/01315st06     Document Type: Article

References (12)

1. n sequence repeats in DNA
2. Nonradioactive gel mobility shift assay using chemiluminescent detection
3. An RNA polymerase II transcription factor binds to an upstream element in the adenovirus major late promoter
4. Nonisotopic gel-mobility shift assay using chemiluminescent detection system
5. Glycosylated DNA-biding proteins from filamentous fungus, Aspergillus oryzae: Modification with N-Acetylglucosamine monosaccharide through an O-Glycosidic linkage
6. Long-range and highly sensitive DNase I footprinting by an automated infrared DNA sequencer
7. Continuous, on-line DNA sequencing using a versatile infrared laser scanner/electrophoresis apparatus
8. Comprehensive cloning and expression analysis of glycolytic genes from the filamentous fungus, Aspergillus oryzae
9. Effects of base mismatches on joining of short oligodeoxynucleotides by DNA ligases
10. Functional elements in the promoter region of the Aspergillus nidulans gpdA gene encoding glyceraldehyde-3-phosphate dehydrogenase
11. A fluorescence based non-radioactive electrophoretic mobility shift assay
12. A sensitive and rapid gel retention assay for nuclear factor I and other DNA-binding proteins in crude nuclear extracts