Deoxyribonuclease I (DNase I)

SKU:BHP15200311
Overview
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Deoxyribonuclease I (DNase I) is a nuclease from ELK Biotechnology. The RNase-free recombinant DNase I hydrolyses single- and double-stranded DNA; digested samples can be used directly in reverse transcription without phenol/chloroform extraction.
Product Type Nucleases & Proteases
Source Recombinant (E. coli)
Activity Hydrolyses ssDNA and dsDNA
RNase Without RNase
Storage Room temperature
Shelf Life 1 year
Grade Research Use Only
Options selector
Catalog no. Size
EQ025-1000U 1000 U (500 uL)
EQ025-2000U 2000 U (1 mL)
EQ025-2000UX10 2000 U x 10
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 1000 U (500 uL), 2000 U (1 mL), 2000 U x 10
  • Lead time: options listed in "Availability Content"; other statuses may take longer.
  • Storage: Room temperature (shelf life 1 year)
  • Shipping: Please contact us to confirm shipping conditions for this product.
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Applications
  • Nucleic Acid Handling
Source Recombinant (E. coli)
Storage Room temperature
Shelf life 1 year
Catalog no. (Mfr.) EQ025
Main SKU BHP15200311
Nucleases & Proteases

Product Overview

Deoxyribonuclease I (DNase I) is a recombinant DNase I protein expressed in E. coli, without RNase. Hydrolysis of single- or double-stranded DNA leaves a phosphate group at the 5' end and a hydroxyl group at the 3' end. DNase I activity is dependent on calcium ions and can be activated by magnesium ions or divalent manganese ions. In the presence of magnesium ions, DNase I can randomly cleave any site of double-stranded DNA; in the presence of divalent manganese ions, DNase I can cleave DNA double-strands at the same site to form blunt ends or short sticky ends with 1–2 nucleotide overhangs.

The enzyme is supplied as a single reagent rather than a kit, in packs of 1000 U (500 µL) and 2000 U (1 mL). Documented uses are removal of DNA contamination from RNA samples, elimination of DNA template after transcription, nick translation, DNase I footprinting for protein–DNA interaction studies, generation of random DNA fragment libraries and use as a positive control in apoptosis TUNEL assays.

Specifications

Format Single reagent, recombinant DNase I solution
Source Recombinant (E. coli)
RNase content Without RNase
Substrate Single- or double-stranded DNA
Cofactor requirement Activity is dependent on calcium ions
Activation by Mg²⁺ Random cleavage at any site of double-stranded DNA
Activation by Mn²⁺ Cleavage of both strands at the same site, giving blunt ends or 1–2 nucleotide overhangs
Product ends 5' phosphate group and 3' hydroxyl group

Applications

  • Removal of DNA contamination from RNA samples and of DNA template after transcription
  • Nick translation
  • DNase I footprinting for protein–DNA interaction studies
  • Generation of random DNA fragment libraries
  • Positive control in apoptosis TUNEL assays

Key Features

  • No cumbersome phenol/chloroform extraction or inactivation is required after digestion.
  • The digested sample can be used directly in a reverse transcription reaction, which is fast and easy to use.

Storage & Handling

Stored at room temperature with a shelf life of one year.

Safety & Regulatory

For research use only. Not intended for clinical, diagnostic or therapeutic use. Follow the manufacturer's manual and standard laboratory safety practice.

GradeResearch Use Only
ManufacturerELK Biotechnology
Catalog No.EQ025
BioHippo SKUBHP15200311
Q.How should the DNase I be stored and how long is the shelf life?
A.The product is stored at room temperature and the shelf life is one year.
Q.What is supplied in the pack?
A.The product is supplied as a single reagent rather than a kit. The manual documents a pack of 1000 U in 500 µL of recombinant DNase I solution; a 2000 U (1 mL) size is also sold. Confirm with BioHippo whether a reaction buffer is included before ordering.
Q.Which ions does the enzyme require?
A.Activity is dependent on calcium ions. Magnesium ions allow random cleavage at any site of double-stranded DNA, while divalent manganese ions cause cleavage of both strands at the same site.
Q.What ends does the digestion leave?
A.Hydrolysis of single- or double-stranded DNA leaves a phosphate group at the 5' end and a hydroxyl group at the 3' end. With manganese ions the products are blunt ends or 1–2 nucleotide overhangs.
Q.Does the digested sample need clean-up before reverse transcription?
A.No. The manufacturer states that no phenol/chloroform extraction or inactivation is needed after digestion and that the digested sample can be used directly in a reverse transcription reaction.
Q.Is this product for research use only?
A.Yes. The manual states that the product is for research use only.

Customization & Add-ons: Need this molecular biology reagent tailored to your workflow? We can help with bulk or custom pack sizes, alternative formats (spin column, magnetic bead or reagent-only kits; premixed or stand-alone reference dye), matched extraction, cDNA synthesis and qPCR workflows, and sourcing of related enzymes, ladders and consumables not in our catalog. Click Talk to a Scientist to submit a request, email us at support@biohippo.com, or explore our Research Services — our team will follow up with feasibility details and next steps.

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