Use of gel retardation to analyze protein-nucleic acid interactions.
about
Efficient translation of rotavirus mRNA requires simultaneous interaction of NSP3 with the eukaryotic translation initiation factor eIF4G and the mRNA 3' endChoosing a suitable method for the identification of replication origins in microbial genomesBHK cell proteins that bind to the 3' stem-loop structure of the West Nile virus genome RNAAccumulation of H/ACA snoRNPs depends on the integrity of the conserved central domain of the RNA-binding protein Nhp2p.A capillary electrophoresis mobility shift assay for protein-DNA binding affinities free in solution.From an electrophoretic mobility shift assay to isolated transcription factors: a fast genomic-proteomic approach.Multiplexed massively parallel SELEX for characterization of human transcription factor binding specificitiesIdentification of the domains of UreR, an AraC-like transcriptional regulator of the urease gene cluster in Proteus mirabilis.A model for the molecular organisation of the IS911 transpososome.Specific interaction of IHF with RIBs, a class of bacterial repetitive DNA elements located at the 3' end of transcription units.Practical strategies for the evaluation of high-affinity protein/nucleic acid interactionsTwo distinct, sequence-specific DNA-binding proteins interact independently with the major replication pause region of sea urchin mtDNA.Induced fit of a peptide loop of methionyl-tRNA formyltransferase triggered by the initiator tRNA substrateEffect of the non-conserved N-terminus on the DNA binding activity of the yeast TATA binding protein.The competence transcription factor of Bacillus subtilis recognizes short A/T-rich sequences arranged in a unique, flexible pattern along the DNA helix.Chemical synthesis of a fully active transcriptional repressor protein.Characterization of MarR, the repressor of the multiple antibiotic resistance (mar) operon in Escherichia coli.Snapshot blotting: transfer of nucleic acids and nucleoprotein complexes from electrophoresis gels to grids for electron microscopy.Activation and repression of transcription at two different phage phi29 promoters are mediated by interaction of the same residues of regulatory protein p4 with RNA polymeraseBinding of DnaA protein to a replication enhancer counteracts the inhibition of plasmid R6K gamma origin replication mediated by elevated levels of R6K pi proteinSynergistic binding of the Vibrio fischeri LuxR transcriptional activator domain and RNA polymerase to the lux promoter region.Transcriptional regulation by TrsN of conjugative transfer genes on staphylococcal plasmid pGO1A multi-parametric flow cytometric assay to analyze DNA-protein interactions.The A1 x U72 base pair conserved in eukaryotic initiator tRNAs is important specifically for binding to the eukaryotic translation initiation factor eIF2.Strand-invasion of duplex DNA by peptide nucleic acid oligomers.Purification and characterization of transcription factors.Protein p4 represses phage phi 29 A2c promoter by interacting with the alpha subunit of Bacillus subtilis RNA polymerase.TMEM8 - a non-globin gene entrapped in the globin web.Biochemical and structural insights into RNA binding by Ssh10b, a member of the highly conserved Sac10b protein family in Archaea.Vaccinia virion protein VP8, the 25 kDa product of the L4R gene, binds single-stranded DNA and RNA with similar affinity.IS911 transpososome assembly as analysed by tethered particle motion.Specificity of RNA binding by CPEB: requirement for RNA recognition motifs and a novel zinc fingerImproving the predictive value of the competence transcription factor (ComK) binding site in Bacillus subtilis using a genomic approach.Reorganization of terminator DNA upon binding replication terminator protein: implications for the functional replication fork arrest complex.Opine-regulated promoters and LysR-type regulators in the nopaline (noc) and octopine (occ) catabolic regions of Ti plasmids of Agrobacterium tumefaciensRole of the imp operon of the Streptomyces coelicolor genetic element SLP1: two imp-encoded proteins interact to autoregulate imp expression and control plasmid maintenance.Integrated microfluidic approach for quantitative high-throughput measurements of transcription factor binding affinities.Poly(A) binding protein, C-terminally truncated by the hepatitis A virus proteinase 3C, inhibits viral translation.The proneural proteins Atonal and Scute regulate neural target genes through different E-box binding sites.The beta recombinase of plasmid pSM19035 binds to two adjacent sites, making different contacts at each of them.
P2860
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P2860
Use of gel retardation to analyze protein-nucleic acid interactions.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Use of gel retardation to analyze protein-nucleic acid interactions.
@ast
Use of gel retardation to analyze protein-nucleic acid interactions.
@en
type
label
Use of gel retardation to analyze protein-nucleic acid interactions.
@ast
Use of gel retardation to analyze protein-nucleic acid interactions.
@en
prefLabel
Use of gel retardation to analyze protein-nucleic acid interactions.
@ast
Use of gel retardation to analyze protein-nucleic acid interactions.
@en
P2093
P2860
P1476
Use of gel retardation to analyze protein-nucleic acid interactions.
@en
P2093
P2860
P304
P577
1992-12-01T00:00:00Z