Gene Regulation
Humana Press Inc. (Verlag)
978-1-4939-6288-4 (ISBN)
Comprehensive and broad in their scope, the protocols are useful to researchers in many disciplines including molecular biology, genomics, biochemistry, biomedicine, nutrition, and agricultural sciences.
Gene Regulation.- Isolation of Nuclei for use in Genome-wide DNase Hypersensitivity Assays to Probe Chromatin Structure.- DNase I Digestion of Isolated Nulcei for Genome-Wide Mapping of DNase Hypersensitivity Sites in Chromatin.- Isolation and Analysis of DNA Derived from Nucleosome-Free Regions.- Acquisition of High Quality DNA for Massive Parallel Sequencing by in vivo Chromatin Immunoprecipitation.- Luciferase Assay to Study the Activity of a Cloned Promoter DNA Fragment.- Promoter Deletion Analysis using a Dual-luciferase Reporter System.- Application of mRNA Display for in vitro Selection of DNA-binding Transcription Factor Complexes.- Isolation of Intracellular Protein:DNA Complexes using HaloCHIP; An Antibody Free Alternative to Chromatin Immunoprecipitation.- A Modified Yeast One-Hybrid System for Genome Wide Identification of Transcription Factor Binding Sites.- Identifying Specific Protein--DNA Interactions using SILAC--based Quantitative Proteomics.- Electrophoretic Mobility-Shift and Super-Shift Assays for Studies and Characterization of Protein-DNA Complexes.- Combination of Native and Denaturing PAGE for the Detection of Protein Binding Regions in Long Fragments of Genomic DNA.- Quantitative NanoProteomics Approach for Protein Complex (QNanoPX) using Gold Nanoparticle-based DNA Probe.- Chromatin Assembly and In Vitro Transcription Analyses for Evaluation of Individual Protein Activities in Multicomponent Transcriptional Complexes.- Using FRET to Monitor Protein-induced DNA Bending: The TBP-TATA Complex as a Model System.- Promoter Independent Abortive Transcription Assays Unravel Functional Interactions Between TFIIB and RNA Polymerase.- Fluorescence Cross-correlation Spectroscopy (FCCS) to Observe Dimerization of Transcription Factors in Living Cells.- Nuclear Recruitment Assay as a Tool to validate Transcription Factor Interactions in Mammalian Cells.- Preparation of Cell Lines for Single-Cell Analysis of TranscriptionalActivation Dynamics.- Peptide Microarrays for Profiling of Serine/threonine Kinase Activity of Recombinant Kinases and Lysates of Cells and Tissue Samples.- Immunoaffinity Purification of Protein Complexes from Mammalian Cells.- Simple and Efficient Identification of Chromatin Modifying Complexes and Characterization of Complex Composition.- Heavy Methyl-SILAC Labeling Coupled with Liquid Chromatography and High-resolution Mass Spectrometry to Study the Dynamics of Site-specific Histone Methylation.- Analysis of p300 Occupancy at the Early Stage of Stem Cell Differentiation by Chromatin Immunoprecipitation.- Mammalian Two-Hybrid Assays for Studies of Interaction of p300 with Transcription Factors.- Fluorescence Anisotropy Microplate Assay to Investigate the Interaction of Full-length Steroid Receptor Coactivator-1a with Steroid Receptors.- Use of Histone Deacetylase Inhibitors to Examine the Roles of Bromodomain and Histone Acetylation in p300-dependent Gene Expression.- Histone Deacetylases Valproic Acid as a Small Molecule Inducer to Direct the Differentiation of Pluripotent Stem Cells.- Sedimentation and Immunoprecipitation Assays for Analyzing Complexes that Repress Transcription.- Methods for Studies of Protein Interactions with Different DNA Methyltransferases.
Erscheinungsdatum | 24.07.2016 |
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Reihe/Serie | Methods in Molecular Biology ; 977 |
Zusatzinfo | 19 Illustrations, color; 61 Illustrations, black and white; XV, 401 p. 80 illus., 19 illus. in color. |
Verlagsort | Totowa, NJ |
Sprache | englisch |
Maße | 178 x 254 mm |
Themenwelt | Sachbuch/Ratgeber ► Natur / Technik ► Naturführer |
Medizin / Pharmazie ► Medizinische Fachgebiete | |
Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik | |
Naturwissenschaften ► Biologie ► Genetik / Molekularbiologie | |
ISBN-10 | 1-4939-6288-4 / 1493962884 |
ISBN-13 | 978-1-4939-6288-4 / 9781493962884 |
Zustand | Neuware |
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