AGAR GEL ELECTROPHORESIS;
ARTICLE;
BINDING AFFINITY;
CONTROLLED STUDY;
CRISPR CAS SYSTEM;
DISSOCIATION CONSTANT;
DNA FOOTPRINTING;
DNA PROTEIN COMPLEX;
ESCHERICHIA COLI;
GEL;
GEL MOBILITY SHIFT ASSAY;
IMAGE ANALYSIS;
NONHUMAN;
POLYACRYLAMIDE GEL ELECTROPHORESIS;
PRIORITY JOURNAL;
PROTEIN DNA INTERACTION;
PROTEIN NUCLEIC ACID INTERACTION;
QUANTITATIVE ANALYSIS;
GENETICS;
IMAGE PROCESSING;
METABOLISM;
PLASMID;
PROCEDURES;
STAINING;
Interference by clustered regularly interspaced short palindromic repeat (CRISPR) RNA is governed by a seed sequence
Semenova E et al (2011) Interference by clustered regularly interspaced short palindromic repeat (CRISPR) RNA is governed by a seed sequence. Proc Natl Acad Sci 108:10098–10103
Analysis of DNA– protein interactions: From nitrocellulose fi lter binding assays to microarray studies
Helwa R, Hoheisel J (2010) Analysis of DNA– protein interactions: from nitrocellulose fi lter binding assays to microarray studies. Anal Bioanal Chem 398:2551–2561
Optical methods to study protein-DNA interactions in vitro and in living cells at the single-molecule level
Monico C et al (2013) Optical methods to study protein-DNA interactions in vitro and in living cells at the single-molecule level. Int J Mol Sci 14:3961–3992
H-NS-mediated repression of CRISPR-based immunity in Escherichia coli K12 can be relieved by the transcription activator LeuO
Westra ER et al (2010) H-NS-mediated repression of CRISPR-based immunity in Escherichia coli K12 can be relieved by the transcription activator LeuO. Mol Microbiol 77:1380–1393
CRISPR immunity relies on the consecutive binding and degradation of negatively supercoiled invader DNA by Cascade and Cas 3
Westra ER et al (2012) CRISPR immunity relies on the consecutive binding and degradation of negatively supercoiled invader DNA by Cascade and Cas 3. Mol Cell 46:595–605