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RQ1 RNase-Free DNase

Degrades Single-Stranded or Double-Stranded DNA

  • Produces 3´ hydroxyl oligonucleotides during degradation
  • Preparation qualified for use in applications where maintaining the integrity of RNA is critical
  • Supplied at a concentration of 1u/μl

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Catalog number: M6101

RQ1 RNase-Free DNase is a preparation of deoxyribonuclease (DNase) I that degrades single-stranded or double-stranded DNA to produce 3´-hydroxyl oligonucleotides. The enzyme is provided with 10X Reaction Buffer (400mM Tris-HCl [pH 8.0 at 25°C], 100mM MgSO4, 10mM CaCl2) and Stop Buffer (20mM EGTA [pH 8.0 at 25°C])


  • Preparation of DNA-free RNA.
  • Degradation of DNA from RNA transcription systems.
  • Nick translation of DNA.
  • Studying DNA:protein interactions by DNase I footprinting.

Storage Buffer: 10mM HEPES (pH 7.5 at 25°C), 50% (v/v) glycerol, 10mM CaCl2, 10mM MgCl2.

Source: Bovine pancreas.

QC Tests: Activity, RNase.

Unit Definition: One unit is defined as the amount of enzyme required to completely degrade 1μg of DNA in 10 minutes at 37°C in 50μl of a buffer containing 40mM Tris-HCl (pH 7.9 at 25°C), 10mM NaCl, 6mM MgCl2, 10mM CaCl2.


Complete Protocol

RQ1 RNase-Free DNase Product Information
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What’s in the box?
Size: 1,000u

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Use Restrictions

For Laboratory Use. Outside of the United States, this product is intended for research use only unless otherwise stated.

Storage Conditions