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  2. MNase-seq - Wikipedia

    en.wikipedia.org/wiki/MNase-seq

    At sufficient concentrations, DNase I is capable of digesting nucleosome-bound DNA to 10bp, whereas micrococcal nuclease cannot. [17] Additionally, DNase-seq is used to identify DHSs, which are regions of DNA that are hypersensitive to DNase treatment and are often indicative of regulatory regions (e.g. promoters or enhancers). [57]

  3. DNase footprinting assay - Wikipedia

    en.wikipedia.org/wiki/DNase_footprinting_assay

    A DNase footprinting assay [1] is a DNA footprinting technique used in molecular biology/biochemistry that detects DNA-protein interaction by leveraging the fact that a protein bound to DNA often protects it from enzymatic cleavage. This makes it possible to locate a protein binding site on a particular DNA molecule.

  4. Deoxyribonuclease I - Wikipedia

    en.wikipedia.org/wiki/Deoxyribonuclease_I

    Deoxyribonuclease I (usually called DNase I), is an endonuclease of the DNase family coded by the human gene DNASE1. [5] DNase I is a nuclease that cleaves DNA preferentially at phosphodiester linkages adjacent to a pyrimidine nucleotide, yielding 5'-phosphate-terminated polynucleotides with a free hydroxyl group on position 3', on average producing tetranucleotides.

  5. Deoxyribonuclease - Wikipedia

    en.wikipedia.org/wiki/Deoxyribonuclease

    The body begins to attack itself as an inflammatory response encompasses the human body. As a result, high levels of ecDNA have been associated with the bloodstream and therefore, researchers have looked to DNase as an appropriate treatment. Studies have shown that DNase was successful in disrupting NETs and decreasing inflammatory responses ...

  6. Hi-C (genomic analysis technique) - Wikipedia

    en.wikipedia.org/wiki/Hi-C_(genomic_analysis...

    The key adaptation to the base protocol was the removal of the SDS solubilization step after digestion to preserve nuclear structure and prevent random ligation between fragmented chromatin by ligation within the intact nuclei, which formed the basis of in situ Hi-C. [12] In 2021, Hi-C 3.0 was described by Lafontaine et al., with higher ...

  7. DNA footprinting - Wikipedia

    en.wikipedia.org/wiki/DNA_footprinting

    It is a good cleavage agent for footprinting because its size makes it easily physically hindered. Thus is more likely to have its action blocked by a bound protein on a DNA sequence. In addition, the DNase I enzyme is easily controlled by adding EDTA to stop the reaction. There are however some limitations in using DNase I.

  8. Micrococcal nuclease - Wikipedia

    en.wikipedia.org/wiki/Micrococcal_nuclease

    Micrococcal nuclease (EC 3.1.31.1, S7 Nuclease, MNase, spleen endonuclease, thermonuclease, nuclease T, micrococcal endonuclease, nuclease T', staphylococcal nuclease, spleen phosphodiesterase, Staphylococcus aureus nuclease, Staphylococcus aureus nuclease B, ribonucleate (deoxynucleate) 3'-nucleotidohydrolase) is an endo-exonuclease that preferentially digests single-stranded nucleic acids.

  9. DNase-Seq - Wikipedia

    en.wikipedia.org/wiki/DNase-Seq

    DNase-seq (DNase I hypersensitive sites sequencing) is a method in molecular biology used to identify the location of regulatory regions, based on the genome-wide sequencing of regions sensitive to cleavage by DNase I. [1] [2] [3] FAIRE-Seq is a successor of DNase-seq for the genome-wide identification of accessible DNA regions in the genome ...