The Experts below are selected from a list of 87 Experts worldwide ranked by ideXlab platform
Mark S. Dodson - One of the best experts on this subject based on the ideXlab platform.
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Dimethyl suberimidate cross-linking of oligo(dT) to DNA-binding proteins.
Bioconjugate chemistry, 2000Co-Authors: Mark S. DodsonAbstract:Dimethyl suberimidate is a bifunctional reagent that is used for cross-linking the protein components of oligomeric macromolecules. In this report, dimethyl suberimidate is shown to specifically cross-link oligo(dT) of varying lengths to the DNA-binding subunits of a multimeric helicase-primase encoded by herpes simplex virus type 1. This result indicates that dimethyl suberimidate and other Imidoester cross-linking reagents may be useful for characterizing the interaction of oligo(dT) with proteins that bind single-stranded DNA.
H. Bock - One of the best experts on this subject based on the ideXlab platform.
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Liquid-crystalline and electron-deficient coronene oligocarboxylic esters and imides by twofold benzogenic Diels-Alder reactions on perylenes.
Chemistry (Weinheim an der Bergstrasse Germany), 2007Co-Authors: Sonia Alibert‐fouet, Isabelle Séguy, Jean-françois Bobo, P. Destruel, H. BockAbstract:Alkyl esters, imides and imido-esters of coronene-tri-, -tetraand-octacarboxylic acids are accessible by a twofold oxidative benzogenic Diels–Alder reaction. Alkyl acrylates add to perylene, and maleic alkyl imides react twice with perylene as well as with perylene-tetracarboxylictetraesters. Coronenes substituted with a greatly variable number of electron with drawing substituents are thus accessible, and di- and tetraimide derivatives are shown to be very pronounced electron-acceptor materials. The triand tetraalkyl esters and Imidoesters self-assemble into columnar liquid-crystalline phases.
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Liquid-Crystalline and Electron-Deficient Coronene Oligocarboxylic Esters and Imides By Twofold Benzogenic Diels–Alder Reactions on Perylenes
Chemistry - A European Journal, 2007Co-Authors: S. Alibert-fouet, Isabelle Séguy, Jean-françois Bobo, P. Destruel, H. BockAbstract:Alkyl esters, imides and imido-esters of coronene-tri-, -tetraand-octacarboxylic acids are accessible by a twofold oxidative benzogenic Diels–Alder reaction. Alkyl acrylates add to perylene, and maleic alkyl imides react twice with perylene as well as with perylene-tetracarboxylictetraesters. Coronenes substituted with a greatly variable number of electron with drawing substituents are thus accessible, and di- and tetraimide derivatives are shown to be very pronounced electron-acceptor materials. The triand tetraalkyl esters and Imidoesters self-assemble into columnar liquid-crystalline phases.
Paul A. Wade - One of the best experts on this subject based on the ideXlab platform.
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Use of bifunctional cross-linking reagents in mapping genomic distribution of chromatin remodeling complexes.
Methods, 2004Co-Authors: Naoyuki Fujita, Paul A. WadeAbstract:Chromatin remodeling complexes consist of multiple subunits, some of which are in intimate contact with DNA while others are not. The ability to effectively cross-link proteins to DNA with formaldehyde is impacted by the average distance between the two species. Productive cross-linking of proteins not in direct contact with DNA is greatly facilitated by the inclusion of an initial cross-linking reaction using bifunctional Imidoester cross-linking reagents.
Naoyuki Fujita - One of the best experts on this subject based on the ideXlab platform.
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Use of bifunctional cross-linking reagents in mapping genomic distribution of chromatin remodeling complexes.
Methods, 2004Co-Authors: Naoyuki Fujita, Paul A. WadeAbstract:Chromatin remodeling complexes consist of multiple subunits, some of which are in intimate contact with DNA while others are not. The ability to effectively cross-link proteins to DNA with formaldehyde is impacted by the average distance between the two species. Productive cross-linking of proteins not in direct contact with DNA is greatly facilitated by the inclusion of an initial cross-linking reaction using bifunctional Imidoester cross-linking reagents.
S. Alibert-fouet - One of the best experts on this subject based on the ideXlab platform.
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Liquid-Crystalline and Electron-Deficient Coronene Oligocarboxylic Esters and Imides By Twofold Benzogenic Diels–Alder Reactions on Perylenes
Chemistry - A European Journal, 2007Co-Authors: S. Alibert-fouet, Isabelle Séguy, Jean-françois Bobo, P. Destruel, H. BockAbstract:Alkyl esters, imides and imido-esters of coronene-tri-, -tetraand-octacarboxylic acids are accessible by a twofold oxidative benzogenic Diels–Alder reaction. Alkyl acrylates add to perylene, and maleic alkyl imides react twice with perylene as well as with perylene-tetracarboxylictetraesters. Coronenes substituted with a greatly variable number of electron with drawing substituents are thus accessible, and di- and tetraimide derivatives are shown to be very pronounced electron-acceptor materials. The triand tetraalkyl esters and Imidoesters self-assemble into columnar liquid-crystalline phases.
