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10.1016/bs.mie.2016.01.002

http://scihub22266oqcxt.onion/10.1016/bs.mie.2016.01.002
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suck abstract from ncbi


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pmid27372747
      Methods+Enzymol 2016 ; 573 (ä): 3-41
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  • In Vitro Chromatin Assembly: Strategies and Quality Control #MMPMID27372747
  • Muthurajan U ; Mattiroli F ; Bergeron S ; Zhou K ; Gu Y ; Chakravarthy S ; Dyer P ; Irving T ; Luger K
  • Methods Enzymol 2016[]; 573 (ä): 3-41 PMID27372747 show ga
  • Chromatin accessibility is modulated by structural transitions that provide timely access to the genetic and epigenetic information during many essential nuclear processes. These transitions are orchestrated by regulatory proteins that coordinate intricate structural modifications and signaling pathways. In vitro reconstituted chromatin samples from defined components are instrumental in defining the mechanistic details of such processes. The bottleneck to appropriate in vitro analysis is the production of high quality, and quality-controlled, chromatin substrates. In this chapter, we describe methods for in vitro chromatin reconstitution and quality control. We highlight the strengths and weaknesses of various approaches and emphasize quality control steps that ensure reconstitution of a bona fide homogenous chromatin preparation. This is essential for optimal reproducibility and reliability of ensuing experiments using chromatin substrates.
  • |*Chromatin Assembly and Disassembly [MESH]
  • |Animals [MESH]
  • |Chromatin/chemistry/genetics [MESH]
  • |DNA/analysis/genetics [MESH]
  • |Fluorescent Dyes/analysis [MESH]
  • |Histones/analysis/genetics [MESH]
  • |Humans [MESH]
  • |Micrococcal Nuclease/metabolism [MESH]
  • |Microscopy, Atomic Force/methods [MESH]
  • |Models, Molecular [MESH]
  • |Native Polyacrylamide Gel Electrophoresis/methods [MESH]
  • |Nucleosomes/chemistry/genetics [MESH]
  • |Protein Folding [MESH]
  • |Protein Multimerization [MESH]
  • |Scattering, Small Angle [MESH]
  • |Ultracentrifugation/methods [MESH]


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