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Description
- 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
Specifications
Specifications
| Concentration | 1 U/μL |
| Components | RQ1 DNase 10X Reaction Buffer 1 x 1mL, RQ1 DNase Stop Solution 1 x 1mL, RQ1 RNase-Free Dnase 1 x 1000U |
| pH | 7.5 |
| For Use With (Application) | 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 | 20mM HEPES (7.5 pH), 10mM CaCl2, 10mM MgCl2, 50% Glycerol |
| Content And Storage | -30°C to -10°C |
| Source | Bovine pancreas |
| Quantity | 1000 U |
| Product Type | RQ1 RNase-free DNase |
| Form | Liquid |
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