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Combination of native and denaturing PAGE for the detection of protein binding regions in long fragments of genomic DNA
BACKGROUND: In a traditional electrophoresis mobility shift assay (EMSA) a (32)P-labeled double-stranded DNA oligonucleotide or a restriction fragment bound to a protein is separated from the unbound DNA by polyacrylamide gel electrophoresis (PAGE) in nondenaturing conditions. An extension of this m...
Autores principales: | Kaer, Kristel, Mätlik, Kert, Metsis, Madis, Speek, Mart |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2435560/ https://www.ncbi.nlm.nih.gov/pubmed/18533036 http://dx.doi.org/10.1186/1471-2164-9-272 |
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