Titlebook: DNA-Protein Interactions; Principles and Proto Beno?t Leblanc,Tom Moss Book 2009Latest edition Humana Press 2009 Chromatin immunoprecipitat

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書目名稱DNA-Protein Interactions影響因子(影響力)




書目名稱DNA-Protein Interactions影響因子(影響力)學(xué)科排名




書目名稱DNA-Protein Interactions網(wǎng)絡(luò)公開(kāi)度




書目名稱DNA-Protein Interactions網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書目名稱DNA-Protein Interactions被引頻次




書目名稱DNA-Protein Interactions被引頻次學(xué)科排名




書目名稱DNA-Protein Interactions年度引用




書目名稱DNA-Protein Interactions年度引用學(xué)科排名




書目名稱DNA-Protein Interactions讀者反饋




書目名稱DNA-Protein Interactions讀者反饋學(xué)科排名

原諒

Audiometry

DNase I Footprinting,using bulky nucleases such as DNAse I. The DNAse I footprinting method was developed to make use of this phenomenon in the study of DNA–protein interactions; it consists in comparing the pattern of fragments produced by the partial digestion of DNA in the absence of a protein to that produced by par

palpitate

Exonuclease III Footprinting on Immobilized DNA Templates, protects it from degradation by an enzyme or chemical reagent..Exonuclease III is a suitable probe to analyze the boundaries of a protein when it is necessary to eliminate any excess unbound DNA from the reaction to avoid background problems. In combination with biotin-labeled DNA that is bound to

Neolithic

Hydroxyl Radical Footprinting of Protein-DNA Complexes,cts between a protein and its cognate DNA and details of the complex structure. We describe several methods to prepare DNA templates for footprinting and ways to avoid many of the pitfalls associated with the use of hydroxyl radical footprinting. In addition, we describe in detail one example of the

Flounder

Flounder

Uranyl Photofootprinting,elength ultraviolet light (. = 300–420 nm), uranyl ions bound to backbone phosphates oxidize proximal sugars and induce nucleic acid backbone cleavage. Thus the uranyl(VI) ion functions as a very specific and efficient photochemical probe for identifying ligand(protein)-phosphate contacts in nucleic

Incorporate

Identification of Protein/DNA Contacts with Dimethyl Sulfate: Methylation Protection and Methylatiol probes, such as dimethyl sulfate, have been used to obtain information on these sites of interaction. Protection and interference patterns frequently correspond to highly conserved positions within binding sites and are often specific for a given transcription factor or family of factors. The meth

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高射炮

Identification of Nucleic Acid High-Affinity Binding Sequences of Proteins by SELEX,rtitioning assay. Here, a histidine-tagged protein is allowed to interact with a pool of nucleic acids and the protein–nucleic acid complexes formed are retained on a Ni-NTA matrix. Nucleic acids with a low level of recognition by the protein are washed away. The pool of recovered nucleic acids is a