نتایج جستجو برای: electrophoretic mobility shift assay

تعداد نتایج: 446161  

2017
Jinlyung Choi Dawn M. Klingeman Steven D. Brown Chris D. Cox

BACKGROUND Clostridium thermocellum utilizes a wide variety of free and cellulosomal cellulases and accessory enzymes to hydrolyze polysaccharides present in complex substrates. To date only a few studies have unveiled the details by which the expression of these cellulases are regulated. Recent studies have described the auto regulation of the celC operon and determined that the celC-glyR3-lic...

Journal: :RNA 2007
Bei-Wen Ying Dominique Fourmy Satoko Yoshizawa

We present here the use of fluorescent methodologies for structural and functional studies of RNA in place of radioactivity. The methods are highly sensitive and quantitative with the use of an infrared fluorescence imaging system. IRD-700 and IRD-800 labels are used for fluorescence detection. Chemical probing methods are largely used for mapping RNA secondary structure and to monitor ligand i...

Journal: :Nucleic acids research 1995
T K Hale A W Braithwaite

We have investigated the transcription factor requirements for basal expression of the mouse p53 promoter by using a combination of reporter and electrophoretic mobility shift assays (EMSAs). We have found that only four regions of the promoter bind transcription factors in EMSAs, suggesting that these are the only important factors for basal transcription. These factors are NF1, USF, ETF-like ...

Journal: :Cold Spring Harbor protocols 2012
Michael F Carey Craig L Peterson Stephen T Smale

This article describes experimental strategies for cloning or identifying genes encoding DNA-binding proteins. DNA-binding proteins are most commonly identified by electrophoretic mobility-shift assay (EMSA) or DNase I footprinting. To identify the gene encoding a protein detected by EMSA or DNase footprinting, the protein often needs to be purified and its sequence analyzed, as described here....

Journal: :Journal of immunology 2001
R Dzialo-Hatton J Milbrandt R D Hockett C T Weaver

Inducible expression of Fas ligand (CD95 ligand) by activated T cells and the resulting apoptosis of CD95-bearing cells is a critical component of peripheral T cell homeostasis and cytotoxic effector mechanisms. Transcriptional control of the expression of Fas ligand has been attributed to a number of factors, including early growth response gene 2 (Egr2), Egr3, Sp1, and NF-AT, although a direc...

2015
Lijun Wang Weiwei Wang Fudong Li Jiahai Zhang Jihui Wu Qingguo Gong Yunyu Shi

Small RNA OxyS is induced during oxidative stress in Escherichia coli and it is an Hfq-dependent negative regulator of mRNA translation. OxyS represses the translation of fhlA and rpoS mRNA, which encode the transcriptional activator and σ(s) subunit of RNA polymerase, respectively. However, little is known regarding how Hfq, an RNA chaperone, interacts with OxyS at the atomic level. Here, usin...

Journal: :The Journal of biological chemistry 1993
S Li H Pelka L H Schulman

A gel shift assay that distinguishes the aminoacylated form from the deacylated form of tRNAs was used to study the requirements for aminoacylation of Escherichia coli tRNA(Asn) in vivo. tRNA(Asn) derivatives containing single base changes in their anticodons or discriminator bases were constructed, and the extent of in vivo aminoacylation was determined directly. Substitution of U35 with C35 o...

2012
Valentina Calvenzani Barbara Testoni Giuliana Gusmaroli Mariangela Lorenzo Nerina Gnesutta Katia Petroni Roberto Mantovani Chiara Tonelli

BACKGROUND NF-Y is a transcription factor that recognizes with high specificity and affinity the widespread CCAAT box promoter element. It is formed by three subunits: NF-YA and the NF-YB/NF-YC- heterodimer containing histone fold domains (HFDs). We previously identified a large NF-Y gene family in Arabidopsis thaliana, composed of 29 members, and characterized their expression patterns in vari...

2013
Sarah E. Altschuler Karen A. Lewis Deborah S. Wuttke

The quantitative evaluation of binding interactions between proteins and nucleic acids is highly sensitive to a variety of experimental conditions. Optimization of these conditions is critical for obtaining high quality, reproducible data, particularly in the context of very high affinity interactions. Here, we discuss the practical considerations involved in optimizing the apparent binding con...

Journal: :Genetics and molecular research : GMR 2013
Jun Ma M G Wang A H Mao J Y Zeng Y Q Liu X Q Wang Jin Ma Y J Tian N Ma N Yang L Wang S Q Liao

Aptamers that recognize the IgG Fc region are of great interest because of their wide application as an immunology probing tool, for diagnostics, and as affinity agents for antibody purification. We developed a target replacement strategy as a modification of conventional Systematic Evolution of Ligands by EXponential enrichment (SELEX) in order to efficiently select and identify novel DNA apta...

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