This Week's Special Recommendation: DNase I

DNase I, or Deoxyribonuclease I, is an endonuclease capable of digesting both single-stranded and double-stranded DNA, producing deoxyribonucleotides or single-stranded or double-stranded oligodeoxyribonucleotides.

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DNase I

DNase I, or Deoxyribonuclease I, is an endonuclease capable of digesting both single-stranded and double-stranded DNA, producing deoxyribonucleotides or single-stranded or double-stranded oligodeoxyribonucleotides. The hydrolysis products of DNase I have a 5' phosphate group and a 3' hydroxyl group. DNase I activity is calcium-dependent and can be activated by magnesium or divalent manganese ions. In the presence of magnesium ions, DNase I randomly cleaves double-stranded DNA at any site. In the presence of divalent manganese ions, DNase I cleaves both strands of DNA at the same site, generating blunt ends or sticky ends with 1-2 nucleotide overhangs.

 

Catalog Number: UA070036

Name: DNase I

Specifications: 1 KU / 5 KU

Enzyme Activity Definition: One unit of activity is defined as the amount of enzyme required to completely degrade 1 µg of pBR322 DNA in 10 minutes at 37°C.

 

 

The results of 1μg pBR322 plasmid digestion separated under different quantity of DnaseⅠ, The reaction was incubated for 10 minutes at 37°C, and 1% agarose gel was used for electrophoresis analysis after reaction.

M, marker;

Lane 1 1μg pBR322;

Lane 2 1μg pBR322 add 4U DNase I

Lane 3 1μg pBR322 add 2U DNase I

Lane 4 1μg pBR322 add 1U DNase I

Lane 5 1μg pBR322 add 0.5U DNase I

Lane 6 1μg pBR322 add 0.25U DNase I

Lane 7 1μg pBR322 add 0.125U DNase I

 

Applications of DNase I

1. DNA Removal During RNA Extraction

2. Preparation of DNA-Free Templates for Reverse Transcription and Degradation of DNA Templates Post-Transcription

3. Digestion of DNA Probes During rRNA Removal

4. Footprinting Analysis of DNA-Protein Interactions

5. Positive Control for DNA Cleavage in TUNEL Assays for Apoptosis Detection

 

For more newly launched tool enzymes, click on the product catalog numbers below to access detailed information on our official website.

This article is reviewed and published by the technical expert team of UA

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