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DN25

Deoxyribonuclease I from bovine pancreas

lyophilized powder, Protein ≥85 %, ≥400 Kunitz units/mg protein

Deoxyribonuclease I from bovine pancreas
1 of 3 reviewers received a sample product or took part in a promotion

Synonym(s):

Deoxyribonuclease, DNase I, Deoxyribonucleate 5′-oligonucleotido-hydrolase

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About This Item

CAS Number:
UNSPSC Code:
12352204
NACRES:
NA.54
EC Number:
232-667-0
MDL number:
EC Number:
Specific activity:
≥400 Kunitz units/mg protein
Biological source:
bovine pancreas
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biological source

bovine pancreas

Quality Level

form

lyophilized powder

specific activity

≥400 Kunitz units/mg protein

mol wt

~31 kDa

composition

Protein, ≥85%

technique(s)

DNA extraction: suitable

solubility

0.15 M NaCl: soluble 5.0 mg/mL, hazy

suitability

suitable for molecular biology

application(s)

diagnostic assay manufacturing

foreign activity

RNase ≤0.02%

shipped in

wet ice

storage temp.

−20°C

General description

DNase I, or Deoxyribonuclease I, is an endonuclease isolated from bovine pancreas.
  • Our DNase I Digests double str and single stranded DNA into oligo and mononucleotides.
  • Bovine pancreatic DNase exists as four isozymes, having isoelectric points for A, B, C and D: 5.22, 4.96, 5.06 and 4.78.3. The predominant form is A, with smaller amounts of B and C, and only minor amount of D.
  • DNase I structure resembles the structure of to exonuclease III. It includes two central β sheets. Each β sheet is composed of six β-strands. This complex of β sheets is surrounded by extensive loop and α-helical regions. This enzyme shares structural similarity to exonuclease III.[1]

Application

  • Decreases viscosity providing better yields by removing DNA in primary cell isolation:
  • Incorporating labelled bases into DNA: DNA nick
  • Radioactive labelling
  • Bioprocessing applications: DNA removal
  • Eliminating genomic DNA from RNA preparations before RT-PCR
  • In vitro transcription
  • Nick translation
  • DNase footprinting
  • Actin regulation of actin polymerization in cells, and cell apoptosis
  • UV crosslinking of proteins to nucleic acids
  • DNase play a role in the regulation of actin polymerization in cells and is involved in apoptosis process [1]
Used for the removal of DNA from protein samples.

Biochem/physiol Actions

DNase I is an endonuclease that acts on phosphodiester bonds adjacent to pyrimidines to produce polynucleotides with terminal 5′-phosphates. In the presence of Mg2+, DNAse I cleaves each strand of DNA independently and the cleavage sites are random. Both DNA strands are cleaved at approximately the same site in the presence of Mn2+. Divalent cations such as Mn2+, Ca2+, Co2+, and Zn2+ are activators of the enzyme. A concentration of 5 mM Ca2+ stabilizes the enzyme against proteolytic digestion. The pH optimum is found to be between 7 and 8. DNAse I from bovine pancreas consists of four chromatographically distinguishable components, A, B, C, and D, with their molar ratios being 4:1:1 respectively. Only minor amounts of D are found.[1] 2-Mercaptoethanol, chelators, sodium dodecyl sulfate (SDS)[2] and actin[3] are known to inhibit the enzyme activity.

Features and Benefits

Our Deoxyribonuclease DNAse I,is essentially RNAse free product, which support the product application.

Physical form

Crude preparation, contains calcium chloride

Preparation Note

10 mg/mL solution of DNAse I in 0.15 M NaCl may lose <10% of its activity when stored for a week in aliquots at −20 °C. The same solutions stored in aliquots at 2-8 °C can lose approximately 20% activity. It remains active for up to five hours at 60 °C between pH 5 and 7, and loses activity in <10 minutes at 68 °C. It loses activity at the rate of 6%/hour in acetate buffer (pH 5.0) and tris buffer ((pH 7.2) at 1 mg/mL concentration.

Analysis Note

Protein determined by biuret.

Other Notes

One Kunitz unit will produce a change in A260 of 0.001 per min per mL at pH 5.0 at 25 °C, using DNA, Type I or III, as substrate.

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This Item
D4527D4513D4263
biological source

bovine pancreas

biological source

bovine pancreas

biological source

bovine pancreas

biological source

bovine pancreas

specific activity

≥400 Kunitz units/mg protein

specific activity

≥2,000 units/mg protein

specific activity

≥2,000 units/mg protein

specific activity

1700—2300 U/vial

technique(s)

DNA extraction: suitable

technique(s)

DNA extraction: suitable

technique(s)

DNA purification: suitable

technique(s)

DNA extraction: suitable

application(s)

diagnostic assay manufacturing

application(s)

diagnostic assay manufacturing

application(s)

diagnostic assay manufacturing

application(s)

diagnostic assay manufacturing

form

lyophilized powder

form

lyophilized powder

form

lyophilized powder

form

powder

suitability

suitable for molecular biology

suitability

suitable for molecular biology

suitability

suitable for molecular biology

suitability

suitable for molecular biology


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pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Resp. Sens. 1

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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Purification of rat spermatogenic cells and preliminary biochemical analysis of these cells.
M L Meistrich et al.
Biology of reproduction, 25(5), 1065-1077 (1981-12-01)
Enzymes of Molecular Biology
Weir, A.F.
Methods in Molecular Biology, 16(2), 2-16 null
Murali Muniraju et al.
Journal of virology, 93(16) (2019-05-31)
Kaposi sarcoma-associated herpesvirus (KSHV) is an emerging pathogen and is the causative infectious agent of Kaposi sarcoma and two malignancies of B cell origin. To date, there is no licensed KSHV vaccine. Development of an effective vaccine against KSHV continues



Global Trade Item Number

SKUGTIN
FTP9814204054839230615
FTP9889804054839199660
DN25-10MG04061835544349
DN25-100MG04061835556687
DN25-5G04061833591673
DN25-1G04061835556694

Questions

1–6 of 6 Questions  
  1. What is the salt tolerance of this DNase I?

    1 answer
    1. This product is not tested for salt tolerance, and therefore, data is not available.

      Helpful?

  2. I would like to know if this product can be used to eliminate DNA from cells in tissue culture (12 wells chamber slide) before immunofluorescent staining? if it can be used - how?

    1 answer
    1. This product can be used to eliminate DNA from cells in tissue culture. Concentration and incubation time should be optimized based on the specific application.

      Helpful?

  3. HOW CAN I PRESERVE DN25 DILUTED and filtered in culture medium? 4C or -20 C?. It will lose activity?

    1 answer
    1. This product is soluble in 0.15 M NaCl at 5 mg/mL. Solutions prepared at 10 mg/mL in 0.15 M NaCl may lose up to 10% activity when stored for 1 week in aliquots at –20 °C. The same solutions stored in aliquots at 2-8 °C can lose up to 20% activity. Please see the link below to review the product datasheet for additional information:
      https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/233/818/dn25pis-ms.pdf

      Helpful?

  4. What is the recommended method for long-term storage of the 1 gram bottle of DN25 in solution?

    1 answer
    1. The user bulletin provides guidance on the storage of DNase I once reconstituted. When stored in aliquots at -20°C, solutions of DNase I at 10 mg/mL in 0.15 M NaCl may lose 10% of activity over a week, while storing the same solutions at 2–8°C can result in a 20% activity loss. Alternatively, maintaining solutions at a minimum concentration of 1 mg protein/mL with 5 mM calcium chloride at -20°C can retain 90% activity for at least a year. Solutions with 0.1 mg protein/mL are less stable and may need gelatin as a stabilizer.
      For applications not affected by glycerol, two storage buffer options are available as they do not freeze at -20°C:
      • 20 mM sodium acetate (pH 6.5) with 5 mM CaCl2, 0.1 mM phenylmethylsulfonyl fluoride (PMSF), and 50% (v/v) glycerol, containing DNase I at 5 mg/mL.
      • 10 mM Tris-HCl (pH 7.5) with 50 mM NaCl, 10 mM MgCl2, 1 mM DTT, and 50% (v/v) glycerol, with DNase I at 2 mg/mL.

      Helpful?

  5. Hi I use the DNase during isolation of cells from lung tissue. Do I need to filter the DNase solution before usage?

    1 answer
    1. This is not a sterile product. If sterility is required due to the specific application, solutions may be filter sterilized before use. Please see the link below to review the product datasheet:
      https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/233/818/dn25pis-ms.pdf

      Helpful?

  6. I use the DNase when I isolate lung cells from lung. Do I need to filter them before I use? I will culture the isolated lung cells.

    1 answer
    1. Yes, please filter the DNase solution before use in cell culture, preferably with a 0.22 um filter. The powder is not sterilized as provided.

      Helpful?

Reviews

1–2 of 3 Reviews  

Active Filters

  1. AZ
    • Review 1
    • Votes 4
    5 out of 5 stars.

    Good in DNA removal during protein production.

    We use it for lysis in protein production and it works well for us.

    Helpful?

  2. Denver, CO
    • Review 1
    • Votes 2
    5 out of 5 stars.

    DNASe 1

    This reagent works well for our purpose in our cell culture prep for cardiomyocytes

    Helpful?

  3. 1 Ratings-only review