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  • Book
    edited by Benoit P. Leblanc and Sebastien Rodrigue.
    Contents:
    Electrophoretic mobility shift assay using radiolabeled DNA probes
    In vitro DNase i footprinting
    Determining the architecture of a protein-DNA complex by combining FeBABE cleavage analyses, 3-D printed structures, and the ICM molsoft program
    In cellulo DNA analysis: LMPCR footprinting
    Southwestern blotting assay
    Single-molecule approaches for the characterization of riboswitch folding mechanisms
    Probing of nascent riboswitch transcripts
    Functional studies of DNA-protein interactions using fret techniques
    Precise identification of genome-wide transcription start sites in bacteria by 5'-rapid amplification of cDNA ends (5'-RACE)
    Analysis of DNA supercoiling induced by DNA-protein interactions
    Precise identification of DNA-binding proteins genomic location by exonuclease coupled chromatin immunoprecipitation (ChIP-exo)
    The cruciform DNA mobility shift assay: A tool to study proteins that recognize bent DNA
    Individual and sequential chromatin immunoprecipitation protocols
    Chromatin endogenous cleavage (ChEC) as a method to quantify protein interaction with genomic DNA in saccharomyces cerevisiae
    Selection and validation of spacer sequences for CRISPR-Cas9 genome editing and transcription regulation in bacteria
    Detection of short-range DNA interactions in mammalian cells using high-resolution circular chromosome conformation capture coupled to deep sequencing
    Global mapping of open chromatin regulatory elements by formaldehyde-assisted isolation of regulatory elements followed by sequencing (FAIRE-seq)
    Aggregate and heatmap representations of genome-wide localization data using VAP, a versatile aggregate profiler
    Circular dichroism for the analysis of protein-DNA interactions
    Quantitative investigation of protein-nucleic acid interactions by biosensor surface plasmon resonance
    Identification of nucleic acid high affinity binding sequences of proteins by SELEX.
    Digital Access Springer 2015
  • Book
    volume editor, Rubin Battino ; evaluators, Rubin Battino ... [et al.] ; compilers, Ardis L. Cramer ... [et al.].
    Digital Access ScienceDirect, 1981
  • Article
    Sicart R, Sable-Amplis R, Fons R.
    Comp Biochem Physiol B. 1978;61(1):77-80.
    1. The amounts of tissue lipids were higher in S. etruscus than in C. russula. 2. The level of liver phospholipids was specially low in C. russula, 2650 mg/100 g as opposed to 3725 g in S. etruscus. 3. This is in good agreement with a reduced rate of the labelled acetate incorporation into the lipids of C. russula. 4. The proportion of unsaturated fatty acids was greater in the liver of S. etruscus; however, the percentage of arachidonic acid was higher in C. russula--15% as opposed to 8%.
    Digital Access Access Options