Definitions
from The American Heritage® Dictionary of the English Language, 5th Edition.
- noun An enzyme that catalyzes the hydrolysis of DNA.
from the GNU version of the Collaborative International Dictionary of English.
- noun (Biochem.) any of numerous enzymes that catalyze the breakdown of DNA into oligonucleotides or mononucleotides.
from Wiktionary, Creative Commons Attribution/Share-Alike License.
- noun biochemistry
deoxyribonuclease
Etymologies
from The American Heritage® Dictionary of the English Language, 4th Edition
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Examples
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To test this hypothesis, I added DNase to the crude extract in which we monitored ATP - and ubiquitin-dependent degradation of BSA, that was used as one of our model substrates.
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Manufactured in clean room conditions BRAND PCR products are DNase, DNA - and
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CAD (or caspase-activated DNase in full) by slicing apart other proteins holding it at bay.
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DNA was removed in two steps, on-column using Qiagen RNase-free DNase and after elution using RNase-free DNase (New England Biolabs).
PLoS ONE Alerts: New Articles Jean-Baptiste Rioux et al. 2010
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CAD (or caspase-activated DNase in full) by slicing apart other proteins holding it at bay.
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Upon completion, the reaction mixtures were treated with DNase RQ1 (Promega) at
PLoS ONE Alerts: New Articles Michel V. L�vesque et al. 2010
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The contiguous primers annealing to the common exon of the B19 genome were used for both DNA and RNA detection, the latter after DNase treatment.
PLoS ONE Alerts: New Articles Claudia Filippone et al. 2010
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They have discovered that the novel effect of caspase 3 in stem cells is related to its ability to activate another protein that cuts up the cell's DNA (called caspase-activated DNase) and has also traditionally been associated with programmed cell death.
PhysOrg.com - latest science and technology news stories 2010
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They have discovered that the novel effect of caspase 3 in stem cells is related to its ability to activate another protein that cuts up the cell's DNA (called caspase-activated DNase) and has also traditionally been associated with programmed cell death.
innovations-report 2010
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On-column DNase I digestion was performed. 100 ng of each RNA sample was retrotranscribed with QuantiTect Whole Transcriptome Kit (Qiagen) and a 50-fold dilution of cDNAs was analyzed by quantitative Real Time PCR (qRT-PCR) using an iCycler-iQ5
PLoS ONE Alerts: New Articles Simone Pacini et al. 2010
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