Cargando…
A 96-well DNase I footprinting screen for drug–DNA interactions
The established protocol for DNase I footprinting has been modified to allow multiple parallel reactions to be rapidly performed in 96-well microtitre plates. By scrutinizing every aspect of the traditional method and making appropriate modifications it has been possible to considerably reduce the t...
Autores principales: | Ellis, Tom, Evans, David A., Martin, Christopher R. H., Hartley, John A. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1919508/ https://www.ncbi.nlm.nih.gov/pubmed/17586817 http://dx.doi.org/10.1093/nar/gkm467 |
Ejemplares similares
-
Wellington: a novel method for the accurate identification of digital genomic footprints from DNase-seq data
por: Piper, Jason, et al.
Publicado: (2013) -
Multiplex indexing approach for the detection of DNase I hypersensitive sites in single cells
por: Gao, Weiwu, et al.
Publicado: (2021) -
Real-time PCR mapping of DNaseI-hypersensitive sites using a novel ligation-mediated amplification technique
por: Follows, George A., et al.
Publicado: (2007) -
A reliable method to display authentic DNase I hypersensitive sites at long-ranges in single-copy genes from large genomes
por: Pipkin, Matthew E., et al.
Publicado: (2006) -
Fast Fenton footprinting: a laboratory-based method for the time-resolved analysis of DNA, RNA and proteins
por: Shcherbakova, Inna, et al.
Publicado: (2006)