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AMPD1

Sigma-Aldrich

DNase I

Amplification Grade

Synonym(s):
Deoxyribonuclease I
Enzyme Commission number:
NACRES:
NA.55

Quality Level

form

liquid

concentration

1 unit/μL

color

colorless

shipped in

wet ice

storage temp.

−20°C

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This Item
101041590011128493200104536282001
DNase I Amplification Grade

Sigma-Aldrich

AMPD1

DNase I

DNase I grade II, from bovine pancreas

Roche

10104159001

DNase I

DNase I from bovine pancreas

Roche

11284932001

DNase I

DNase I recombinant grade I, from bovine pancreas, expressed in Pichia pastoris

Roche

04536282001

DNase I recombinant

concentration

1 unit/μL

concentration

-

concentration

-

concentration

-

color

colorless

color

-

color

-

color

-

shipped in

wet ice

shipped in

-

shipped in

-

shipped in

-

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

100

General description

Deoxyribonuclease I (DNase I) is an endonuclease isolated from bovine pancreas that digests double and single stranded DNA into oligo and mononucleotides. Amplification Grade DNase I has been purified to remove RNase activity, and is suitable for eliminating DNA from RNA preparations prior to sensitive applications, such as RT-PCR (Reverse Transcriptase - Polymerase Chain Reaction).

DNase I digests double- and single-stranded DNA into oligo- and mononucleotides. Using the Reaction Buffer provided, DNA is removed from RNA preparations in a 15 minute digestion at room temperature. The DNase I is then inactivated by heating with the Stop Solution. Heating also denatures hairpins in the RNA, so the RNA can be used directly in reverse transcription.

No current RNA isolation procedure removes 100% of the DNA. Many commercial DNase I formulations are contaminated with residual RNases. This RNase contamination can destroy or degrade valuable RNA samples prior to reverse transcription. Laboratory comparisons have shown that Sigma′s Amplification Grade DNase I demonstrates lower RNase activity than that from several leading molecular biology product suppliers.

Application

Amplification grade DNase I has been used:
  • for the digestion of DNA during isolation and purification of RNA. The purified RNA can be used for the synthesis of cDNA using RNA reverse transcriptase.
  • to hydrolyze extracellular matrix (ECM) components and enhance photosensitizer penetration into the biofilm to determine the efficacy of antimicrobial photodynamic therapy (aPDT) on Candida albicans biofilms
  • to remove contaminating DNA from total RNA extracted from cattle blood samples

Features and Benefits

  • Suitable for the elimination of DNA from RNA
  • Minimal RNase activity available
  • Optimized 10× reaction buffer and Stop Solution for complete inactivation of DNase I

Suitability

Suitable for use in removing DNA from RNA preparations.

Unit Definition

One unit completely digests 1 μg of plasmid DNA to oligonucleotides in 10 min. at 37 °C.

Legal Information

Purchase of this product is accompanied by a limited license for use in the Polymerase Chain Reaction (PCR) process for research purposes only and in conjunction with a thermal cycler whose use in the automated performance of the PCR process is covered by an up-front license fee, either by payment to Applied Biosystems or as purchased, i.e., and authorized thermal cycler.

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Hafid Ait-Oufella et al.
The Journal of experimental medicine, 207(8), 1579-1587 (2010-07-07)
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Runting-stunting syndrome (RSS) in chickens, also known as malabsorption syndrome, which is characterized by mild to severe enteritis and diagnosed through typical histopathologic examination as well as clinical signs, results in considerable economic losses. Despite the many studies carried out
Ling Yuan et al.
Molecular vision, 18, 1684-1695 (2012-07-10)
The objectives of this study were to determine whether high-glucose-induced upregulation of heparanase (HPSE) expression and differential heparanase expression in human retinal vascular endothelial cells (HRECs) can alter HREC migration and proliferation. We also aimed to determine whether HREC migration
John P Dunbar et al.
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The noble false widow spider Steatoda nobilis originates from the Macaronesian archipelago and has expanded its range globally. Outside of its natural range, it may have a negative impact on native wildlife, and in temperate regions it lives in synanthropic
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