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Scientific Article | Ce protocole décrit en détail la préparation des complexes nucléosomiques à l’aide de deux méthodes de préparation des échantillons
DNA repair in the context of chromatin is poorly understood. Biochemical studies using nucleosome core particles, the fundamental repeating unit of chromatin, show most DNA repair enzymes remove DNA damage at reduced rates as compared to free DNA.
Nucleosome core particle dimers. (A) Representative cryo-EM raw
Genome-wide mapping and cryo-EM structural analyses of the
Electron microscopy analysis of ATP-independent nucleosome
Preparation of Nucleosome Core Particles Complexed with DNA Repair
Cryo-EM structure of the nucleosome containing the ALB1 enhancer
Cryo-EM structure of SWI/SNF complex bound to a nucleosome
Structural and mechanistic insights into the DNA glycosylase AAG
Structural basis for APE1 processing DNA damage in the nucleosome
Self-Assembly of Geometry-Based DNA Origami-Histone Protein Hybrid
Cryo-EM data processing a, Data processing procedure for the
Asymmetric nucleosome PARylation at DNA breaks mediates
Chromatin structure meets cryo-EM: Dynamic building blocks of the
High-resolution structure determination of sub-100 kDa complexes
Cryo-EM structure of the nucleosome containing the ALB1 enhancer