Titlebook: Chromatin Protocols; Srikumar P. Chellappan Book 2009Latest edition Humana Press 2009 Chromatin immunoprecipitation (ChIP) assays.DNA.DNA

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Analysis of DNA Topology in Yeast Chromatin,gy that reflect alterations in chromatin structure can be measured and quantified using closed circular plasmids from living yeast. Here we describe detailed protocols for measuring DNA topology in yeast chromatin.

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Monitoring DNA Breaks in Optically Highlighted Chromatin in Living Cells by Laser Scanning Confocalins has provided spatial and temporal details concerning the establishment of biochemical subnuclear regions geared toward metabolizing genomic lesions. A specific marker for chromatin regions containing DNA breaks is required to study the initial dynamic structural changes in chromatin when DNA bre

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Analysis of Genomic Aberrations Using Comparative Genomic Hybridization of Metaphase Chromosomes, and amplifications are detected, which are likely to indicate regions harboring tumor suppressor and oncogenes. CGH involves the extraction of test and reference (karyotypically normal) DNA. These samples are whole-genome amplified by DOP-PCR and then differentially labeled with fluorophores via ni

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In Vitro Replication Assay with Mammalian Cell Extracts,d the complex mammalian replication system is the cell-free in vitro replication assay (IVRA). IVRA can provide a snapshot of the regulatory mechanisms controlling replication in higher eukaryotes by using a single plasmid, pEPI-1. This chapter outlines the general strategies and protocols used to p

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Investigation of Genomic Methylation Status Using Methylation-Specific and Bisulfite Sequencing Polenomic methylation of cytosines within CpG dinucleotides is crucial to development, gene silencing and chromosome inactivation. Importantly, aberrant methylation profiles of various genes are associated with cancer and potentially autoimmune disease, brain-related disease, diabetes and heart disease

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Biochemical Analysis of Arginine Methylation in Transcription,tion such as transcriptional activation and repression, mRNA processing and nuclear-cytoplasmic shuttling. This modification is catalyzed by the PRMT family of enzymes which utilize intracellular .-adenosyl methionine as a cofactor to dimethylate-specific arginines found within many target proteins.